Team:Potsdam Bioware/Labjournal/August part 2

From 2011.igem.org

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Line 87: Line 87:
<b>Materials</b><br>
<b>Materials</b><br>
-
* DNA of pSB1T3 clones and different promotors (Ara, IPTG, constitutive)
+
* DNA of pSB1T3 clones and different promotors (Ara, Lac, constitutive)
* restriction enzymes: EcoRI, XbaI
* restriction enzymes: EcoRI, XbaI
Line 259: Line 259:
<br>
<br>
-
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Ligation of pSB1T3 backbones with Ara, IPTG and constitutive promotors</h3>
+
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Ligation of pSB1T3 backbones with Ara, Lac and constitutive promotors</h3>
<b>Investigators:</b> Nicole, Jessica, Katharina<br>
<b>Investigators:</b> Nicole, Jessica, Katharina<br>
Line 289: Line 289:
** constitutive promotor
** constitutive promotor
-
** IPTG-Promotor
+
** Lac-Promotor
* water
* water
Line 339: Line 339:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;">Site directed mutagenesis of Precission protease to remove iGEM restriction sites from the protease and introduction of iGEM restriction sites</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;">Site directed mutagenesis of 14_3C protease to remove iGEM restriction sites from the protease and introduction of iGEM restriction sites</h3>
<b>For better understanding of described experiment see also: [[http://141.89.201.101/iGEM/wiki2011/images/c/c8/UP_SG_Klonierungsschema_Protease.pptx]]</b><br>
<b>For better understanding of described experiment see also: [[http://141.89.201.101/iGEM/wiki2011/images/c/c8/UP_SG_Klonierungsschema_Protease.pptx]]</b><br>
Line 347: Line 347:
<b>Aim:</b><br>
<b>Aim:</b><br>
-
* Removal of iGEM restriction sites from Pre protease, amplifying protease fragments with iGEM restriction sites<br>
+
* Removal of iGEM restriction sites from 14_3C protease, amplifying protease fragments with iGEM restriction sites<br>
<b>Materials:</b><br>
<b>Materials:</b><br>
-
*Plasmid: pGEX-3_PreSiccion
+
*Plasmid: pGEX-3_14_3C
-
*Primers: (1) f_Presiccion_ACCAGC, r_Presiccion_iGEM_BamHI (2) r_PreSiccion_ACCAGC, f_PreSiccion_AraFusion_NgoMIV, (3) f_PreSiccion_tm_Xbal208_A-T, r_PreSiccion_tm_Xbal208_A-T (4)r_PreSiccion_iGEM_BamHI, f_PreSiccion_tm_Xbal280_A-T
+
*Primers: (1) f_14_3C_ACCAGC, r_14_3C_iGEM_BamHI (2) r_14_3C_ACCAGC, f_14_3C_AraFusion_NgoMIV, (3) f_14_3C_tm_Xbal208_A-T, r_14_3C_tm_Xbal208_A-T (4)r_14_3C_iGEM_BamHI, f_14_3C_tm_Xbal280_A-T
<b> Used method: </b>
<b> Used method: </b>
Line 401: Line 401:
Expected Fragments:
Expected Fragments:
-
*PreSiccion_mut_fragI: 153 bp
+
*14_3C_mut_fragI: 153 bp
-
*PreSiccion_mut_fragII: 66 bp
+
*14_3C_mut_fragII: 66 bp
-
*PreSiccion_mut_fragIII: 72 bp
+
*14_3C_mut_fragIII: 72 bp
-
*PreSiccion_mut_fragIV: 260 bp
+
*14_3C_mut_fragIV: 260 bp
<b> Further going: </b>
<b> Further going: </b>
-
*Assembly PCR of purificated products to produce NgoMIV_iGEM_PreSiccion-Protease_iGEM_BamHI (mutated Pre-Fragment)
+
*Assembly PCR of purificated products to produce NgoMIV_iGEM_14_3C-Protease_iGEM_BamHI (mutated 14_3C-Fragment)
<br>
<br>
Line 723: Line 723:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;">Digestion of complete mutated TEV and PreSciccion fragments and 3x-ligation into TEV- or Pre-backbones with amplified and digested AraC fragment</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;">Digestion of complete mutated TEV and 14_3C fragments and 3x-ligation into TEV- or 14_3C-backbones with amplified and digested AraC fragment</h3>
<b>Investigators:</b> Paul, Stefan
<b>Investigators:</b> Paul, Stefan
Line 731: Line 731:
(1)NgoMIV_iGEM_TEV-Protease_iGEM_BamHI
(1)NgoMIV_iGEM_TEV-Protease_iGEM_BamHI
-
(2)NgoMIV_iGEM_PreSiccion-Protease_iGEM_BamHI
+
(2)NgoMIV_iGEM_14_3C-Protease_iGEM_BamHI
(3)HindIII_iGEM_AraC_NgoMIV (digested)
(3)HindIII_iGEM_AraC_NgoMIV (digested)
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* resolving of digested fragments on preparative agarose gel and excission of corresponding bands. Extraction of DNA from the gel was performed using NucleoSping ExtractII KIT.
* resolving of digested fragments on preparative agarose gel and excission of corresponding bands. Extraction of DNA from the gel was performed using NucleoSping ExtractII KIT.
-
Ligation of digested proteases into digested the pJC354-Pre/TEV vectors including the AraC fragment (3)
+
Ligation of digested proteases into digested the pJC354-14_3C/TEV vectors including the AraC fragment (3)
concentrations for ligations were calculated using gibthon ligation calculator: [http://www.gibthon.org/ligate.html CALC]
concentrations for ligations were calculated using gibthon ligation calculator: [http://www.gibthon.org/ligate.html CALC]
Line 777: Line 777:
**pSB1A3-YFP +Ara (clone C) 14: 221.4 ng/µl
**pSB1A3-YFP +Ara (clone C) 14: 221.4 ng/µl
-
**pSB1A3-CFP +IPTG (clone A) 15: 319.3 ng/µl
+
**pSB1A3-CFP +Lac (clone A) 15: 319.3 ng/µl
-
**pSB1A3-CFP +IPTG (clone B) 34: 105.5 ng/µl
+
**pSB1A3-CFP +Lac (clone B) 34: 105.5 ng/µl
-
**pSB1A3-CFP +IPTG (clone C) 33: 135.7 ng/µl
+
**pSB1A3-CFP +Lac (clone C) 33: 135.7 ng/µl
-
**pSB1A3-YFP +IPTG (clone A) 16: 110.6 ng/µl
+
**pSB1A3-YFP +Lac (clone A) 16: 110.6 ng/µl
-
**pSB1A3-YFP +IPTG (clone B) 4: 340.4 ng/µl
+
**pSB1A3-YFP +Lac (clone B) 4: 340.4 ng/µl
-
**pSB1A3-YFP +IPTG (clone C) 13: 290.6 ng/µl
+
**pSB1A3-YFP +Lac (clone C) 13: 290.6 ng/µl
**pSB1A3-CFP + const (clone A) 11: 312.2 ng/µl
**pSB1A3-CFP + const (clone A) 11: 312.2 ng/µl
Line 809: Line 809:
**pSB1K3-YFP +Ara (clone C) 30: 135.1 ng/µl
**pSB1K3-YFP +Ara (clone C) 30: 135.1 ng/µl
-
**pSB1K3-CFP +IPTG (clone A) 20: 138.4 ng/µl
+
**pSB1K3-CFP +Lac (clone A) 20: 138.4 ng/µl
-
**pSB1K3-CFP +IPTG (clone B) 21: 58.3 ng/µl
+
**pSB1K3-CFP +Lac (clone B) 21: 58.3 ng/µl
-
**pSB1K3-CFP +IPTG (clone C) 23: 122.0 ng/µl
+
**pSB1K3-CFP +Lac (clone C) 23: 122.0 ng/µl
-
**pSB1K3-YFP +IPTG (clone A) 29: 69.3 ng/µl
+
**pSB1K3-YFP +Lac (clone A) 29: 69.3 ng/µl
-
**pSB1K3-YFP +IPTG (clone B) 17: 153.1 ng/µl
+
**pSB1K3-YFP +Lac (clone B) 17: 153.1 ng/µl
-
**pSB1K3-YFP +IPTG (clone C) 18: 90.9 ng/µl
+
**pSB1K3-YFP +Lac (clone C) 18: 90.9 ng/µl
**pSB1K3-CFP + const (clone A) 26: 89.8 ng/µl
**pSB1K3-CFP + const (clone A) 26: 89.8 ng/µl
Line 867: Line 867:
<b>Further tasks:</b><br>
<b>Further tasks:</b><br>
-
Ligation with TEV and PreScission and appropriate backbone<br>
+
Ligation with TEV and 14_3C and appropriate backbone<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Ligation and transformation of PreScission with backbone</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Ligation and transformation of 14_3C with backbone</h3>
<b>Investigator:</b> Paul, Stefan<br>
<b>Investigator:</b> Paul, Stefan<br>
Line 875: Line 875:
<b>Aim:</b><br>
<b>Aim:</b><br>
-
*liagte and transform PreScission with AraC and backbone<br>
+
*liagte and transform 14_3C with AraC and backbone<br>
<b>Materials:</b><br>
<b>Materials:</b><br>
Line 1,135: Line 1,135:
<h2 style="background-color: rgb(240, 20, 70);">71th Labday 2011-08-21</h2>
<h2 style="background-color: rgb(240, 20, 70);">71th Labday 2011-08-21</h2>
-
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Transformation of competent RV cells with ligation products of pSB1T3/pSB1C3 backbones with Ara, IPTG and constitutive promotors</h3>
+
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Transformation of competent RV cells with ligation products of pSB1T3/pSB1C3 backbones with Ara, Lac and constitutive promotors</h3>
<b>Investigator:</b> Katharina<br>
<b>Investigator:</b> Katharina<br>
Line 1,211: Line 1,211:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Digest of pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Digest of pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL</h3>
<b>Investigator:</b> Sascha, Sebastian<br>
<b>Investigator:</b> Sascha, Sebastian<br>
Line 1,217: Line 1,217:
<b>Aim:</b><br>
<b>Aim:</b><br>
-
*Digestion of vector pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL for ligation with AraC and PreSciccion protease<br>
+
*Digestion of vector pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL for ligation with AraC and 14_3C protease<br>
<b>Materials:</b><br>
<b>Materials:</b><br>
-
* 4 µl of 3 different fractions of pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL (approx. 1,2-1,5 µg DNA)<br>
+
* 4 µl of 3 different fractions of pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL (approx. 1,2-1,5 µg DNA)<br>
* Restriction enzymes BamHI HF and HindIII (purchased form NEB)<br>
* Restriction enzymes BamHI HF and HindIII (purchased form NEB)<br>
Line 1,233: Line 1,233:
<b>Results:</b><br>
<b>Results:</b><br>
-
* 3 different digested vector fractions of pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL for ligation with AraC and PreSciccion protease<br>
+
* 3 different digested vector fractions of pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL for ligation with AraC and 14_3C protease<br>
<b>Further tasks:</b><br>
<b>Further tasks:</b><br>
Line 1,241: Line 1,241:
<b>Output:</b><br>
<b>Output:</b><br>
-
* pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL vector fraction 1, c= ng/ml<br>
+
* pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL vector fraction 1, c= ng/ml<br>
-
* pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL vector fraction 2, c= ng/ml<br>
+
* pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL vector fraction 2, c= ng/ml<br>
-
* pJC354_ssTorA_NheI_CS-Pre_XhoI_blaFL vector fraction 3, c= ng/ml<br>
+
* pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL vector fraction 3, c= ng/ml<br>
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Assembly PCR of different TEV mutagenesis fraction </h3>
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Assembly PCR of different TEV mutagenesis fraction </h3>
Line 1,975: Line 1,975:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Digest of amplified PreSciccion protease (assembled fragments after sidedirected mutagenesis), amplified AraC (from pBAD_iGEM_express mVenus), plasmid pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL and plasmid pJC354_ssTorA_XhoI_CS-TEV_NheI_blaFL</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Digest of amplified 14_3C protease (assembled fragments after sidedirected mutagenesis), amplified AraC (from pBAD_iGEM_express mVenus), plasmid pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL and plasmid pJC354_ssTorA_XhoI_CS-TEV_NheI_blaFL</h3>
<b>Investigator: </b> Sebastian, Sascha<br>
<b>Investigator: </b> Sebastian, Sascha<br>
Line 1,993: Line 1,993:
* PCR amplified AraC-fragment<br>
* PCR amplified AraC-fragment<br>
-
* PCR amplified and mutated PreSciccion protease<br>
+
* PCR amplified and mutated 14_3C protease<br>
<b>Methode:</b><br>
<b>Methode:</b><br>
Line 2,001: Line 2,001:
<i>Reaction batches:</i><br>
<i>Reaction batches:</i><br>
-
* Batch 1: 21.7 µl PreSciccion fraction I (c=157.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl BamHI, 0.3 µl BSA, 3 µl Buffer 4<br>
+
* Batch 1: 21.7 µl 14_3C fraction I (c=157.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl BamHI, 0.3 µl BSA, 3 µl Buffer 4<br>
-
* Batch 2: 21.7 µl PreSciccion fraction II(c=157.5 ng/µl), 2.5 µl NgoMIV, 2.5 µl BamHI, 0.3 µl BSA, 3 µl Buffer 4<br>
+
* Batch 2: 21.7 µl 14_3C fraction II(c=157.5 ng/µl), 2.5 µl NgoMIV, 2.5 µl BamHI, 0.3 µl BSA, 3 µl Buffer 4<br>
* Batch 3: 22.0 µl AraC (c=175.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl HindIII, 3 µl Buffer 2<br>
* Batch 3: 22.0 µl AraC (c=175.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl HindIII, 3 µl Buffer 2<br>
Line 2,023: Line 2,023:
<b>Output:</b><br>
<b>Output:</b><br>
-
* digested fragments of AraC, PreSciccion protease and plasmid backbones for transformation (AraC + PreSciccion + "PreSciccion-backbone", AraC + TEV + "TEV-backbone")<br>
+
* digested fragments of AraC, 14_3C protease and plasmid backbones for transformation (AraC + 14_3C + "14_3C-backbone", AraC + TEV + "TEV-backbone")<br>
1) EcoRI_AraC_NgoMIV<br>
1) EcoRI_AraC_NgoMIV<br>
Line 2,029: Line 2,029:
2) HindIII_AraC_NgoMIV<br>
2) HindIII_AraC_NgoMIV<br>
-
3) NgoMIV_PreSciccion_BamHI Batch 1<br>
+
3) NgoMIV_14_3C_BamHI Batch 1<br>
-
4) NgoMIV_PreSciccion_BamHI Batch 2<br>
+
4) NgoMIV_14_3C_BamHI Batch 2<br>
5) BamHI_pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL_HindIII Batch 1<br>
5) BamHI_pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL_HindIII Batch 1<br>
Line 2,167: Line 2,167:
**pSB1A3-YFP +Ara (clone C) 14: 221.4 ng/µl
**pSB1A3-YFP +Ara (clone C) 14: 221.4 ng/µl
-
**pSB1A3-CFP +IPTG (clone A) 15: 319.3 ng/µl
+
**pSB1A3-CFP +Lac (clone A) 15: 319.3 ng/µl
-
**pSB1A3-CFP +IPTG (clone B) 34: 105.5 ng/µl
+
**pSB1A3-CFP +Lac (clone B) 34: 105.5 ng/µl
-
**pSB1A3-CFP +IPTG (clone C) 33: 135.7 ng/µl
+
**pSB1A3-CFP +Lac (clone C) 33: 135.7 ng/µl
-
**pSB1A3-YFP +IPTG (clone A) 16: 110.6 ng/µl
+
**pSB1A3-YFP +Lac (clone A) 16: 110.6 ng/µl
-
**pSB1A3-YFP +IPTG (clone B) 4: 340.4 ng/µl
+
**pSB1A3-YFP +Lac (clone B) 4: 340.4 ng/µl
-
**pSB1A3-YFP +IPTG (clone C) 13: 290.6 ng/µl
+
**pSB1A3-YFP +Lac (clone C) 13: 290.6 ng/µl
**pSB1A3-CFP + const (clone A) 11: 312.2 ng/µl
**pSB1A3-CFP + const (clone A) 11: 312.2 ng/µl
Line 2,199: Line 2,199:
**pSB1K3-YFP +Ara (clone C) 30: 135.1 ng/µl
**pSB1K3-YFP +Ara (clone C) 30: 135.1 ng/µl
-
**pSB1K3-CFP +IPTG (clone A) 20: 138.4 ng/µl
+
**pSB1K3-CFP +Lac (clone A) 20: 138.4 ng/µl
-
**pSB1K3-CFP +IPTG (clone B) 21: 58.3 ng/µl
+
**pSB1K3-CFP +Lac (clone B) 21: 58.3 ng/µl
-
**pSB1K3-CFP +IPTG (clone C) 23: 122.0 ng/µl
+
**pSB1K3-CFP +Lac (clone C) 23: 122.0 ng/µl
-
**pSB1K3-YFP +IPTG (clone A) 29: 69.3 ng/µl
+
**pSB1K3-YFP +Lac (clone A) 29: 69.3 ng/µl
-
**pSB1K3-YFP +IPTG (clone B) 17: 153.1 ng/µl
+
**pSB1K3-YFP +Lac (clone B) 17: 153.1 ng/µl
-
**pSB1K3-YFP +IPTG (clone C) 18: 90.9 ng/µl
+
**pSB1K3-YFP +Lac (clone C) 18: 90.9 ng/µl
**pSB1K3-CFP + const (clone A) 26: 89.8 ng/µl
**pSB1K3-CFP + const (clone A) 26: 89.8 ng/µl
Line 2,257: Line 2,257:
** 24.2 µl water
** 24.2 µl water
-
*Reaction mix (IPTG)
+
*Reaction mix (Lac)
** 0.5 µl DNA
** 0.5 µl DNA
Line 2,437: Line 2,437:
|-
|-
-
| 23 || pSB1A3-CFP +IPTG (clone A) || 15||
+
| 23 || pSB1A3-CFP +Lac (clone A) || 15||
|-
|-
-
| 24 || pSB1A3-CFP +IPTG (clone B) || 15||
+
| 24 || pSB1A3-CFP +Lac (clone B) || 15||
|-
|-
-
| 25 || pSB1A3-CFP +IPTG (clone C) || 15||
+
| 25 || pSB1A3-CFP +Lac (clone C) || 15||
|-
|-
-
| 26 || pSB1A3-YFP +IPTG (clone A) || 15||
+
| 26 || pSB1A3-YFP +Lac (clone A) || 15||
|-
|-
-
| 27 || pSB1A3-YFP +IPTG (clone B)|| 15||
+
| 27 || pSB1A3-YFP +Lac (clone B)|| 15||
|-
|-
-
| 28 || pSB1A3-YFP +IPTG (clone C)|| 15||
+
| 28 || pSB1A3-YFP +Lac (clone C)|| 15||
|-
|-
-
| 29 || pSB1K3-CFP +IPTG (clone A)|| 15||
+
| 29 || pSB1K3-CFP +Lac (clone A)|| 15||
|-
|-
-
| 30 || pSB1K3-CFP +IPTG (clone B) || 15||
+
| 30 || pSB1K3-CFP +Lac (clone B) || 15||
|-
|-
-
| 31 || pSB1K3-CFP +IPTG (clone C) || 15||
+
| 31 || pSB1K3-CFP +Lac (clone C) || 15||
|-
|-
-
| 32 || pSB1K3-YFP +IPTG (clone A) || 15||
+
| 32 || pSB1K3-YFP +Lac (clone A) || 15||
|-
|-
-
| 33 || pSB1K3-YFP +IPTG (clone B) || 15||
+
| 33 || pSB1K3-YFP +Lac (clone B) || 15||
|-
|-
-
| 34 || pSB1K3-YFP +IPTG (clone C)|| 15||
+
| 34 || pSB1K3-YFP +Lac (clone C)|| 15||
|-
|-
Line 2,577: Line 2,577:
* digested, gel purified, dephoshorylated vectors: pSB1C3, pSB1T3-YFP I clone c, pSB1T3-YFP II plate 2 clone d
* digested, gel purified, dephoshorylated vectors: pSB1C3, pSB1T3-YFP I clone c, pSB1T3-YFP II plate 2 clone d
-
* Inserts: Ara promoter, IPTG promoter, constitutive promoter
+
* Inserts: Ara promoter, Lac promoter, constitutive promoter
<b> Method:</b>
<b> Method:</b>
Line 2,607: Line 2,607:
** pSB1C3 + Ara
** pSB1C3 + Ara
-
** pSB1C3 + IPTG
+
** pSB1C3 + Lac
** pSB1C3 + const
** pSB1C3 + const
Line 2,615: Line 2,615:
** pSB1T3-YFP II + Ara
** pSB1T3-YFP II + Ara
-
** pSB1T3-YFP II + IPTG
+
** pSB1T3-YFP II + Lac
** pSB1T3-YFP II + const
** pSB1T3-YFP II + const
Line 2,623: Line 2,623:
** pSB1T3-YFP I + Ara
** pSB1T3-YFP I + Ara
-
** pSB1T3-YFP I + IPTG
+
** pSB1T3-YFP I + Lac
** pSB1T3-YFP I + const
** pSB1T3-YFP I + const
Line 2,791: Line 2,791:
<h2 style="background-color: rgb(240, 20, 70);">74th Labday 2011-08-24</h2>
<h2 style="background-color: rgb(240, 20, 70);">74th Labday 2011-08-24</h2>
-
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Transformation w/ pUP089 A and B, BBa_K40304_Affibody_MiddleLinker+Ara/Const/IPTG, pSB1T3+YFPI+Ara/Const/IPTG and pSB1T3+YFPII+Ara/Const/IPTG </h3>
+
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Transformation w/ pUP089 A and B, BBa_K40304_Affibody_MiddleLinker+Ara/Const/Lac, pSB1T3+YFPI+Ara/Const/Lac and pSB1T3+YFPII+Ara/Const/Lac </h3>
<b>Investigators:</b> Nicole, Nadine<br>
<b>Investigators:</b> Nicole, Nadine<br>
Line 2,801: Line 2,801:
* creating pARW089 without Amp resistance, called then pUP089
* creating pARW089 without Amp resistance, called then pUP089
-
* get expression backbones w/ Tet or Cm resistance and Ara, Const. or IPTG promotors
+
* get expression backbones w/ Tet or Cm resistance and Ara, Const. or Lac promotors
<b>Material:</b><br>
<b>Material:</b><br>
Line 2,813: Line 2,813:
** pSB1C3 + Ara
** pSB1C3 + Ara
-
** pSB1C3 + IPTG
+
** pSB1C3 + Lac
** pSB1C3 + const
** pSB1C3 + const
Line 2,821: Line 2,821:
** pSB1T3-YFP II + Ara
** pSB1T3-YFP II + Ara
-
** pSB1T3-YFP II + IPTG
+
** pSB1T3-YFP II + Lac
** pSB1T3-YFP II + const
** pSB1T3-YFP II + const
Line 2,829: Line 2,829:
** pSB1T3-YFP I + Ara
** pSB1T3-YFP I + Ara
-
** pSB1T3-YFP I + IPTG
+
** pSB1T3-YFP I + Lac
** pSB1T3-YFP I + const
** pSB1T3-YFP I + const
Line 3,407: Line 3,407:
<br>
<br>
-
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Transformation w/ pUP089 A and B, BBa_K40304_Affibody_MiddleLinker+Ara/Const/IPTG, pSB1T3+YFPI+Ara/Const/IPTG and pSB1T3+YFPII+Ara/Const/IPTG </h3>
+
<h3 style="background-color: rgb(254, 122, 122); font-weight: bold;">Transformation w/ pUP089 A and B, BBa_K40304_Affibody_MiddleLinker+Ara/Const/Lac, pSB1T3+YFPI+Ara/Const/Lac and pSB1T3+YFPII+Ara/Const/Lac </h3>
<b>Investigators:</b> Nicole, Nadine<br>
<b>Investigators:</b> Nicole, Nadine<br>
Line 3,417: Line 3,417:
* creating pARW089 without Amp resistance, called then pUP089
* creating pARW089 without Amp resistance, called then pUP089
-
* get expression backbones w/ Tet or Cm resistance and Ara, Const. or IPTG promotors
+
* get expression backbones w/ Tet or Cm resistance and Ara, Const. or Lac promotors
<b>Material:</b><br>
<b>Material:</b><br>
Line 3,429: Line 3,429:
** pSB1C3 + Ara
** pSB1C3 + Ara
-
** pSB1C3 + IPTG
+
** pSB1C3 + Lac
** pSB1C3 + const
** pSB1C3 + const
Line 3,437: Line 3,437:
** pSB1T3-YFP II + Ara
** pSB1T3-YFP II + Ara
-
** pSB1T3-YFP II + IPTG
+
** pSB1T3-YFP II + Lac
** pSB1T3-YFP II + const
** pSB1T3-YFP II + const
Line 3,445: Line 3,445:
** pSB1T3-YFP I + Ara
** pSB1T3-YFP I + Ara
-
** pSB1T3-YFP I + IPTG
+
** pSB1T3-YFP I + Lac
** pSB1T3-YFP I + const
** pSB1T3-YFP I + const
Line 3,551: Line 3,551:
** pSB1C3 + Ara
** pSB1C3 + Ara
-
** pSB1C3 + IPTG
+
** pSB1C3 + Lac
** pSB1C3 + const
** pSB1C3 + const
Line 3,559: Line 3,559:
** pSB1T3-YFP II + Ara
** pSB1T3-YFP II + Ara
-
** pSB1T3-YFP II + IPTG
+
** pSB1T3-YFP II + Lac
** pSB1T3-YFP II + const
** pSB1T3-YFP II + const
Line 3,567: Line 3,567:
** pSB1T3-YFP I + Ara
** pSB1T3-YFP I + Ara
-
** pSB1T3-YFP I + IPTG
+
** pSB1T3-YFP I + Lac
** pSB1T3-YFP I + const
** pSB1T3-YFP I + const
Line 3,681: Line 3,681:
** pSB1C3 + Ara
** pSB1C3 + Ara
-
** pSB1C3 + IPTG
+
** pSB1C3 + Lac
** pSB1C3 + const
** pSB1C3 + const
Line 3,689: Line 3,689:
** pSB1T3-YFP II + Ara
** pSB1T3-YFP II + Ara
-
** pSB1T3-YFP II + IPTG
+
** pSB1T3-YFP II + Lac
** pSB1T3-YFP II + const
** pSB1T3-YFP II + const
Line 3,697: Line 3,697:
** pSB1T3-YFP I + Ara
** pSB1T3-YFP I + Ara
-
** pSB1T3-YFP I + IPTG
+
** pSB1T3-YFP I + Lac
** pSB1T3-YFP I + const
** pSB1T3-YFP I + const
Line 3,861: Line 3,861:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> gel purification of AraC, TEV, PreScission and TEv vector and PreScission vector</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> gel purification of AraC, TEV, 14_3C and TEv vector and 14_3C vector</h3>
<b>Investigator: </b> Stefan<br>
<b>Investigator: </b> Stefan<br>
Line 3,877: Line 3,877:
ligation of different fragmentsand transformation of competent E.coli XL1 blue cells.<br>
ligation of different fragmentsand transformation of competent E.coli XL1 blue cells.<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> ligation of AraC, TEV/PreScission with the TEV/PreScission vector</h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> ligation of AraC, TEV/14_3C with the TEV/14_3C vector</h3>
<b>Investigator: </b> Stefan<br>
<b>Investigator: </b> Stefan<br>
Line 3,887: Line 3,887:
|+ optional table caption
|+ optional table caption
-
! Column heading 1 !! TEV 1 µL !! TEV 2 µL !! TEV 3 µL !! TEV 4 µL !! PreScission 1 µL !! PreScission 2 µL !! control PreScission vector µL !! control TEV vector µL !!
+
! Column heading 1 !! TEV 1 µL !! TEV 2 µL !! TEV 3 µL !! TEV 4 µL !! 14_3C 1 µL !! 14_3C 2 µL !! control 14_3C vector µL !! control TEV vector µL !!
|-
|-
Line 5,918: Line 5,918:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Production of TEV and PreSciccion biobricks part 1 </h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Production of TEV and 14_3C biobricks part 1 </h3>
-
Aim: indtroduction of iGEM restriction sites to produced mutated TEV and Pre Fragments.
+
Aim: indtroduction of iGEM restriction sites to produced mutated TEV and 14_3C Fragments.
Primer TEV:
Primer TEV:
Line 5,928: Line 5,928:
(2) r_TEV_ACCAGC, f_TEV_iGEM
(2) r_TEV_ACCAGC, f_TEV_iGEM
-
Primer PRE:
+
Primer 14_3C:
-
(1) f_PreSiccion_ACCAGC, r_PreSiccion_iGEM_Eco81l
+
(1) f_14_3C_ACCAGC, r_14_3C_iGEM_Eco81l
-
(2) r_PreSiccion_ACCAGC, f_PreSiccion_iGEM
+
(2) r_14_3C_ACCAGC, f_14_3C_iGEM
<b>Methode:</b><br>
<b>Methode:</b><br>
Line 5,938: Line 5,938:
PCR<br>
PCR<br>
-
*Template: 1µl (TEV or Pre <10ng)
+
*Template: 1µl (TEV or 14_3C <10ng)
*Nucleotides: 1µl of 10mM ready to use dNTP mix<br>
*Nucleotides: 1µl of 10mM ready to use dNTP mix<br>
Line 6,576: Line 6,576:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> sequencing of TEV and PreScission clones </h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> sequencing of TEV and 14_3C clones </h3>
Aim: get sequences
Aim: get sequences
Line 7,298: Line 7,298:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Assembly PCR for TEV and PreScsiion </h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Assembly PCR for TEV and 14_3C </h3>
-
Aim: get the side-directed mutated TEV and PreScsiion fragment<br>
+
Aim: get the side-directed mutated TEV and 14_3C fragment<br>
<b>Methode:</b><br>
<b>Methode:</b><br>
Line 7,310: Line 7,310:
(2) r_TEV_iGEM_BamHI<br>
(2) r_TEV_iGEM_BamHI<br>
-
Primer PRE:
+
Primer 14_3C:
-
(1) f_PreSiccion_iGEM<br>
+
(1) f_14_3C_iGEM<br>
-
(2) r_PreSiccion_iGEM_BamHI
+
(2) r_14_3C_iGEM_BamHI
<b>Methode:</b><br>
<b>Methode:</b><br>
Line 7,320: Line 7,320:
PCR<br>
PCR<br>
-
*Template: 1 µL (TEV or Pre <10ng)
+
*Template: 1 µL (TEV or 14_3C <10ng)
*Nucleotides: 1 µL of 10 mM ready to use dNTP mix<br>
*Nucleotides: 1 µL of 10 mM ready to use dNTP mix<br>
Line 7,634: Line 7,634:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> gel electrophoresis of TEV and PreScission </h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> gel electrophoresis of TEV and 14_3C </h3>
Aim: check sizes<br>
Aim: check sizes<br>
Line 7,794: Line 7,794:
<br>
<br>
-
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Assembly PCR for PreScsiion, PCR of AraC and TEV </h3>
+
<h3 style="background-color: rgb(100, 150, 100); font-weight: bold;"> Assembly PCR for 14_3C, PCR of AraC and TEV </h3>
-
Aim: get the side-directed mutated TEV and PreSiccion fragment<br>
+
Aim: get the side-directed mutated TEV and 14_3C fragment<br>
<b>Method:</b><br>
<b>Method:</b><br>
Line 7,806: Line 7,806:
(2) r_TEV_iGEM_BamHI<br>
(2) r_TEV_iGEM_BamHI<br>
-
Primer PRE:
+
Primer 14_3C:
-
(1) f_PreSiccion_iGEM<br>
+
(1) f_14_3C_iGEM<br>
-
(2) r_PreSiccion_iGEM_BamHI
+
(2) r_14_3C_iGEM_BamHI
<b>Methode:</b><br>
<b>Methode:</b><br>
Line 7,816: Line 7,816:
PCR<br>
PCR<br>
-
*Template: 1 µL (TEV or Pre <10ng)
+
*Template: 1 µL (TEV or 14_3C <10ng)
*Nucleotides: 1 µL of 10 mM ready to use dNTP mix<br>
*Nucleotides: 1 µL of 10 mM ready to use dNTP mix<br>

Latest revision as of 13:03, 21 September 2011

Contents

66th Labday 2011-08-17

Planning mdnA modification (library)

Investigators: Nicole

Time: 2011-08-17, 20:45

Aim: Planning mdnA library

Materials

  • codon table
  • Kristian's diversity sheet
  • excel

Results:


UP Table mdna libary planning 2011-08-18.png


Output:

Excel Table: Y:\Klonierung\mdna modification\mdna modification 03.xlsx


67th Labday 2011-08-18

Ordering oligos for modified mdnA library

Investigators: Nicole


miniprep of pSB1T3 clones containing CFP and YFP, respectively

Investigators: Nicole, Jessica, Steffi, Katharina

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 30µl
  • Check concentration with NanoDrop

Results:

  • pSB1T3+YFP I clone b: 72.1 ng/µl
  • pSB1T3+YFP I clone c: 53.5 ng/µl
  • pSB1T3+YFP I clone a: 197.1 ng/µl
  • pSB1T3+YFP II plate 1 clone b: 46.1 ng/µl
  • pSB1T3+YFP II clone a: 62.6 ng/µl
  • pSB1T3+YFP II plate 2 clone d: 25.6 ng/µl
  • pSB1T3+YFP II plate 2 clone c: 25.6 ng/µl
  • pSB1T3+YFP I clone d: 101.8 ng/µl

Further Tasks:

  • restriction enzyme digestion
  • ligation with promotors
  • transformation


restriction enzyme digestion of

Investigators: Nicole, Jessica, Katharina

Materials

  • DNA of pSB1T3 clones and different promotors (Ara, Lac, constitutive)
  • restriction enzymes: EcoRI, XbaI
  • NEB Buffer 4
  • water

Method

  • 0.5µl EcoRI
  • 0.5µl XbaI (again 0.5µl were added after 1.5 h)
  • 1000ng DNA
  • water added to total volume of 30µl
  • restriction enzyme digestion overnight at 37°C


Digestion of pak bla KDIR

Investigators: Sabine

Aim:

  • cutting out of geneIII for using as PCR template

Reason:

  • pak bla KDIR contains a part of a myc tag
  • the overhang of the geneIII forward primer contains a complete myc tag for insertion of myc into the phage display vector
  • this may lead to the low yield of geneIII target DNA after PCR using entire vector pak bla KDIR as template

Time: 2011-08-18,10:00-14:00

Materials/Methods:

  • 5 µl pak bla KDIR (ca 4500 ng)
  • 2 µl NEB 10x buffer 2
  • 1 µl restriction enzyme AvaI
  • 1 µ restriction enzyme HindIII
  • 11 µl water
  • 4 h at 37°C

Further tasks:

  • gel electrophoresis for purification of geneIII
  • perform PCR of geneIII


Repeated PCR of mdnA and gene III for phage display (strategy 2)

Investigator: Sabine

Time: 2011-08-18, 15:00-18:00

Aim:

  • amplification of geneIII with NgoMIV and AatII and rfc 25 restriction sites (strategy 2)

Reaction Components:

  • 1 µl / 6 ng DNA (cut out geneIII from pak bla KDIR)
  • 0,25 µl OneTaq Polymerase
  • 1 µl dNTPs
  • 1 µl per primer (pf_geneIII_Xba_NgoMIV_myc and pr_geneIII_iGEM_AatII)
  • 5 µl 5x PCR Buffer
  • 30,75 µl DNase free water


  • purification of PCR fragments with QIAquick Gel Extraction Kit (250)

Further tasks:

  • digestion / ligation


Digestion of pSB1C3

Investigators: Sabine

Aim:

  • cloning of biobricks mdnA, geneIII and mdna/geneIII (fusion gene) into pSB1C3

Time: 2011-08-18,17:30-18:00

Materials/Methods:

  • 8 µl pSB1C3 (ca 2000 ng)
  • 2 µl NEB 10x buffer 2
  • 1 µl restriction enzyme XbaI
  • 1 µ restriction enzyme PstI
  • 0,2 µl BSA
  • 7,8 µl water
  • over night at 37°C

Further tasks:

  • gel electrophoresis for purification
  • ligation of mdnA, geneIII and mdna/geneIII (fusion gene) into pSB1C3


69th Labday 2011-08-19

Clean up of digestion products

Investigators:Katharina

Materials

  • products of restriction enzyme digestion
  • NucleoSpin Extract II Kit from Macherey-Nagel


miniprep of pSB1A3 and pSB1K3 clones containing either CFP or YFP and different promotors

Investigators: Nicole, Jessica, Katharina

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 50µl
  • Check concentration with NanoDrop

Results

  • all concentrations were around 30 ng/µl so the preps were thrown away
  • new overnight cultures have been prepared

Further Tasks:

  • new miniprep
  • confirmation of clones by restriction enzyme digestion
  • sending for sequencing


Ligation of pSB1T3 backbones with Ara, Lac and constitutive promotors

Investigators: Nicole, Jessica, Katharina

Materials

  • T4 DNA Ligase Buffer
  • T4 Ligase Buffer
  • different EcoRi and XbaI digested pSB1T3 backbones
    • pSB1T3+YFP I clone b
    • pSB1T3+YFP I clone a
    • pSB1T3+YFP II plate 1 clone b
    • pSB1T3+YFP II clone a
    • pSB1T3+YFP I clone d: 101.8 ng/µl
  • EcoRI and XbaI digested pSB1C3
  • EcoRI and XbaI digested inserts
    • Ara-Promotor
    • constitutive promotor
    • Lac-Promotor
  • water

Method

  • 1µl 10x T4 DNA Ligase Buffer
  • 1µl T4 DNA Ligase
  • 2µl backbone DNA
  • 5µl insert DNA
  • 1µl water
  • control was prepared for the constructs by taking water instead of insert DNA


Transformation of competent RV cells with Ligation products

Investigators:Jessica, Katharina

Materials

  • ligation products of:
    • pSB1T3+YFPI clone b + different promotors
    • pSB1T3+YFPI clone a + different promotors
    • pSB1T3+YFPII plate 1 clone b + different promotors
    • pSB1C3 + different promotors
  • competent RV cells

Method

  • transformation was done using the heatshock-protocol
  • pSB1T3 clones were plated on LB+agar+Tet
  • pSB1C3 clones were plated on LB+agar+Cm
  • incubation over night at 37°C


Site directed mutagenesis of 14_3C protease to remove iGEM restriction sites from the protease and introduction of iGEM restriction sites

For better understanding of described experiment see also: http://141.89.201.101/iGEM/wiki2011/images/c/c8/UP_SG_Klonierungsschema_Protease.pptx

Investigators: Sascha, Paul, Sebastian

Aim:

  • Removal of iGEM restriction sites from 14_3C protease, amplifying protease fragments with iGEM restriction sites

Materials:

  • Plasmid: pGEX-3_14_3C
  • Primers: (1) f_14_3C_ACCAGC, r_14_3C_iGEM_BamHI (2) r_14_3C_ACCAGC, f_14_3C_AraFusion_NgoMIV, (3) f_14_3C_tm_Xbal208_A-T, r_14_3C_tm_Xbal208_A-T (4)r_14_3C_iGEM_BamHI, f_14_3C_tm_Xbal280_A-T

Used method:

PCR

  • Template: 1µl
  • Nucleotides: 1µl of 10mM ready to use dNTP mix
  • 5µl 10x Amplification buffer S
  • 2µl 25mM MgCl2
  • 2,5µl primers = 25pmol absolute (2,5µl of each primer)
  • 34,5µl of pure water
  • 0,5µl TaqPol

Program:

  • Denat: 3min 94°C
  • 5x:

Denat: 45sec 94°C

Anneal:45sec 53°C

Extend:45sec 72°C

  • 25x:

Denat: 45sec 60°C

Anneal:45sec 60°C

Extend:45sec 72°C

  • Final Extend: 10min 72°C

Result:

Resolving of PCR products on preparative 2% agarose gel, exsciccion of coresponding band and gel exctraction via Nucleospin gel extract II.

Expected Fragments:

  • 14_3C_mut_fragI: 153 bp
  • 14_3C_mut_fragII: 66 bp
  • 14_3C_mut_fragIII: 72 bp
  • 14_3C_mut_fragIV: 260 bp

Further going:

  • Assembly PCR of purificated products to produce NgoMIV_iGEM_14_3C-Protease_iGEM_BamHI (mutated 14_3C-Fragment)


Digestion of PCR products geneIII and mdnA for cloning into pSB1C3

Investigator: Sabine

Aim: cloning of mdnA and geneIII into pSB1C3

Time: 2011-08-19, 10:00-13:00

Material/Method:

  • 30 µl PCR product (990 ng mdnA or 3200 ng geneIII)
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme PstI
  • 0,5 µl BSA
  • 4 µl NEB 10x buffer 2
  • 3,5 µl water
  • 1 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • cloning into pSB1C3


Digestion of PCR products geneIII and mdnA for cloning mdnA/geneIII into pSB1C3 and pARW089

Investigator: Sabine

Aim: cloning of mdnA/geneIII fusion gene into pSB1C3 and pARW089 (2 step ligation)

Time: 2011-08-19, 10:00-13:00

Material/Method:

  • 30 µl / 990 ng mdnA
  • 1 µl restriction enzyme AgeI
  • 4 µl NEB 10x buffer 1
  • 5 µl water
  • 1 h, 37°C


  • 30 µl / 3200 ng geneIII
  • 1 µl restriction enzyme NgoMIV
  • 4 µl NEB 10x buffer 4
  • 5 µl water
  • 1 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • ligation of mdnA and geneIII, than ligation into pSB1C3


Digestion of PCR products geneIII and mdnA for cloning into pARW089 (3 fragment ligation)

Investigator: Sabine

Aim: cloning of mdnA and geneIII into pARW089 (3 fragment ligation)

Time: 2011-08-19, 10:00-13:00

Material/Method:

  • 30 µl / 990 ng mdnA
  • 2 µl restriction enzyme NarI
  • 1 µl restriction enzyme AatII
  • 4 µl NEB 10x buffer 4
  • 3 µl water
  • 1 h, 37°C


  • 30 µl / 3200 ng geneIII
  • 1 µl restriction enzyme NgoMIV
  • 1 µl restriction enzyme AatII
  • 4 µl NEB 10x buffer 4
  • 4 µl water
  • 1 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • ligation into pARW089


Digestion of PCR product mdnA for cloning into pARW089

Investigator: Sabine

Aim: cloning of mdnA into pARW089

Time: 2011-08-19, 10:00-13:00

Material/Method:

  • 30 µl / 990 ng mdnA
  • 2 µl restriction enzyme NarI
  • 1 µl restriction enzyme AatII
  • 4 µl NEB 10x buffer 4
  • 3 µl water
  • 1 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • ligation into pARW089, than digestion with AgeI and NgoMIV and ligation of geneIII


Analysis of sequenced pPDV100

Investigator: Sabine

Aim: control of created pPDV100

Time: 2011-08-19, 14:00-14:15

Result:

  • created vector contains no mdnA

Further Tasks:

  • this strategy will not be further persued


Agarose gel electrophoresis of digested mdnA and geneIII

Investigator: Sabine

Aim: purification of digested DNA fragments

Time: 2011-08-19, 15:00-17:00

Material/Method:

  • digested geneIII, mdnA, pSB1C3
  • 1% agarose gel, loading dye, DNA ladder mix (Fermentas)
  • 100 V

Results:

  • sample mdnA (NarI+AatII) has been lost (ran under the gel)
  • concentration pSB1C3 (Xba+Pst): 17 ng/µl
  • concentration mdnA (AgeI): 3,8 ng/µl
  • concentration mdnA (XbaI+PstI): 5,5 ng/µl
  • concentration geneIII (NgoMIV): 15,5 ng/µl
  • concentration geneIII (XbaI+PstI): 12,2 ng/µl
  • concentration geneIII (NgoMIV+AatII): 12,8 ng/µ

Further Tasks:

  • repeat PCR and digestion of mdnA (NarI+AatII)
  • ligations


Repeated PCR of mdnA

Investigator: Sabine

Time: 2011-08-19,17:00-19:00

Aim:

  • amplification of mdnA with NarI and AgeI restriction sites

Primer:

  • primer: pf_mdnA_iGEM_EheI and pr_mdnA_iGEM_AatII

Reaction Components:

  • 2 µl Vector pARW089 (16 ng)
  • 0,25 µl Taq Polymerase S (BioScience)
  • 1 µl dNTPs
  • 1 µl per primer
  • 5 µl 10x PCR Buffer S
  • 39,75 µl water

Further tasks:

  • purification
  • digestion


Site directed mutagenesis of TEV protease to remove iGEM restriction sites from the protease and introduction of iGEM restriction sites and assembly of produced TEV-fragments

Investigators: Sascha, Paul

  • Mutagenesis was performed as described before in the wiki.
  • 3 reaction batches

Results:

Expected fragments (360bp and 400bp) were excissed and extracted from the gel using Nucleospin Extract Kit

  • Assembly PCR of TEV fragments I and II was performed as described before in the wiki

The expected mutated complete TEV fragment was PCR purificated using nucleospin extract KIT


Amplificarion of arabinose induction system (AraC) from pBAD_iGEMexpress plasmid, produces a 1273bp fragment

Investigators: Sascha, Paul, Sebastian

Materials:

Plasmid: pBAD_iGEMexpress (Nr.4) Primers: f_AraC_HindIII_iGEM , r_AraC_NgoMIV

Used method: PCR

Template: 1µl = 7,2 ng

Nucleotides: 1 µl of 10mM ready to use dNTP mix 5µl 10x

Amplification buffer S: 5µl 25mM MgCl2 2,5µl

primers = 25pmol absolute (2,5µl of each primer = 5µl per tube) 32,5µl of pure water 0,5µl TaqPol

Program: iGEM002

Denat: 3min 94°C

5x:

Denat: 60sec 94°C

Anneal:60sec 53°C

Extend:60sec 72°C

25x:

Denat: 60sec 60°C

Anneal:60sec 60°C

Extend:60sec 72°C

Final Extend: 10min 72°C

  • PCR purification using NucleoSpin Extract KIT and digestion of AraC fragment (1273bp) witth NgoMIV and HindIII
  • Resolving of digested AraC fragment on 1.5% preparative agarose Gel
  • The corresponding band (1273bp) was excissed and extracted from the gel using Nucleospin Extract KIT.

Expected Fragments: HindIII_iGEM_AraC_NgoMIV 1273bp


Digestion of complete mutated TEV and 14_3C fragments and 3x-ligation into TEV- or 14_3C-backbones with amplified and digested AraC fragment

Investigators: Paul, Stefan

Materials:

(1)NgoMIV_iGEM_TEV-Protease_iGEM_BamHI

(2)NgoMIV_iGEM_14_3C-Protease_iGEM_BamHI

(3)HindIII_iGEM_AraC_NgoMIV (digested)

  • digestion of proteases (1) and (2) with NgoMIV and BamHI as described before in the wiki with NgoMIV and BamHI
  • resolving of digested fragments on preparative agarose gel and excission of corresponding bands. Extraction of DNA from the gel was performed using NucleoSping ExtractII KIT.

Ligation of digested proteases into digested the pJC354-14_3C/TEV vectors including the AraC fragment (3)

concentrations for ligations were calculated using gibthon ligation calculator: [http://www.gibthon.org/ligate.html CALC]

  • ligations were allowed to proceed for 1h at room temperature and were immediately transformed into competent XL1-blue cells using standard transformation protocol


70th Labday 2011-08-20

miniprep of pSB1A3 and pSB1K3 clones containing either CFP or YFP and different promotors

Investigator: Jessica, Katharina

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 50µl
  • Check concentration with NanoDrop

Results

  • concentrations:
    • pSB1A3-CFP +Ara (clone A) 12: 342.1 ng/µl
    • pSB1A3-CFP +Ara (clone B) 7: 252.5 ng/µl
    • pSB1A3-CFP +Ara (clone C) 6: 356.9 ng/µl
    • pSB1A3-YFP +Ara (clone A) 1: 339.2 ng/µl
    • pSB1A3-YFP +Ara (clone B) 5: 379.0 ng/µl
    • pSB1A3-YFP +Ara (clone C) 14: 221.4 ng/µl
    • pSB1A3-CFP +Lac (clone A) 15: 319.3 ng/µl
    • pSB1A3-CFP +Lac (clone B) 34: 105.5 ng/µl
    • pSB1A3-CFP +Lac (clone C) 33: 135.7 ng/µl
    • pSB1A3-YFP +Lac (clone A) 16: 110.6 ng/µl
    • pSB1A3-YFP +Lac (clone B) 4: 340.4 ng/µl
    • pSB1A3-YFP +Lac (clone C) 13: 290.6 ng/µl
    • pSB1A3-CFP + const (clone A) 11: 312.2 ng/µl
    • pSB1A3-CFP + const (clone B) 9: 218.0 ng/µl
    • pSB1A3-CFP + const (clone C) 10: 201.7 ng/µl
    • pSB1A3-YFP + const (clone C) 28: 238.0 ng/µl
    • pSB1K3-CFP +Ara (clone A) 25: 175.2 ng/µl
    • pSB1K3-CFP +Ara (clone B) 31: 190.2 ng/µl
    • pSB1K3-CFP +Ara (clone C) 24: 193.8 ng/µl
    • pSB1K3-YFP +Ara (clone A) 22: 119.6 ng/µl
    • pSB1K3-YFP +Ara (clone B) 19: 149.4 ng/µl
    • pSB1K3-YFP +Ara (clone C) 30: 135.1 ng/µl
    • pSB1K3-CFP +Lac (clone A) 20: 138.4 ng/µl
    • pSB1K3-CFP +Lac (clone B) 21: 58.3 ng/µl
    • pSB1K3-CFP +Lac (clone C) 23: 122.0 ng/µl
    • pSB1K3-YFP +Lac (clone A) 29: 69.3 ng/µl
    • pSB1K3-YFP +Lac (clone B) 17: 153.1 ng/µl
    • pSB1K3-YFP +Lac (clone C) 18: 90.9 ng/µl
    • pSB1K3-CFP + const (clone A) 26: 89.8 ng/µl
    • pSB1K3-CFP +const (clone B) 8: 252.5 ng/µl
    • pSB1K3-CFP +const (clone C) 2: 256.6 ng/µl
    • pSB1K3-YFP + const (clone A) 27: 55.7 ng/µl
    • pSB1K3-YFP +const (clone B) 3: 231.9 ng/µl
    • pSB1K3-YFP + const (clone C) 32: 174.9 ng/µl
    • pARW089 35: 333.8 ng/µl
    • pARW089 36: 326.4 ng/µl

Further Tasks:

  • confirmation of clones by restriction enzyme digestion
  • sending for sequencing


Gel extraction of different AraC for TEV approaches

Investigator: Stefan

Aim:

  • purification of DNA

Materials:

  • NucleoSpin Kit (Machery Nagel)

Method:

  • DNA extraction from agarose gels protocol of NucleoSpin Kit

Results:

BILD von Sabine geschickt, von mir eingefügt

Further tasks:

Ligation with TEV and 14_3C and appropriate backbone

Ligation and transformation of 14_3C with backbone

Investigator: Paul, Stefan

Aim:

  • liagte and transform 14_3C with AraC and backbone

Materials:

Transformation Protocol Using Heat Shock

1) Take chemically competent E. coli cells from –80°C freezer.

a. Use XL1-blue cells for all cloning and DNA-related tasks, BL21 cells for protein/peptide expression.

2) Turn on water bath or heat block to 42°C.

3) Competent cells should be in a 1.5 ml tube. For transforming a DNA construct, use 60 ul of competent cells. .

4) Keep tubes on ice.

5) Add DNA solution into the E.coli cell suspension, mix by flicking the tube. Incubate on ice for 15-30 min.

Note: 2 µL from a T4 DNA ligase reaction are usually sufficient

6) Put tubes into heat block at 42°C for 45 seconds.

7) Put tubes back on ice for 2 minutes to reduce damage to the E. coli cells.

8) Add 750 µL of LB or DYT (with no antibiotic!). Incubate tubes for 1 hour at 37°C and 750 rpm.

9) Spread 100 ul of the resulting culture on LB agar plates (with appropriate antibiotic added!).

Note: In case of "tricky" ligations which yield few colonies, spin down the cell suspension for 3 min at 6000 rcf (since you can't spread 800 µL), discard most of the supernatant, resuspend the bacterial pellet by pipetting and use this for spreading.

10) Grow overnight at 37 °C.

11) Pick colonies about 12-16 hours later.

Method:


Results:

check clones via colony PCR for correct insert

Further tasks:

sequencing postive clones

production of competent E. coli XL 1 blue

Investigator: Stefan

Aim:

  • competent E. coli XL 1 blue

Materials:

  • CaCl2
  • E. coli XL1 blue

Method:

Work always sterile and cold and speedy!

  • All volumes deal with the common cell line!
  • The cooling-centrifuge is in the tool shed , cool down to 4°C early enough , close the lid correctly!
  • Prepare early enough min. 100 Eppis (1,5µl) (per cellline) and cool down to -80°C before using
  • Use Milipore-filter for sterile CaCl2 , keep cool!
  • prepare 15ml LB-Medium (or DYT) with the specific antibiotic (XL1-blue? Tet, BL21 ? none!), inoculate and incubate over night
  • prepare 200ml LB-Medium (or DYT) with the specific antibiotic, inoculate with 2ml of the over-night-culture. Nurture the culture until OD600 at 0,35 (0,2-0,5) (if the OD is too high, the cell won’t be competent)
  • keep cell suspension in sterile falcons (50ml) 20 min on ice, then centrifuge for 20min; 4°C; 2500g
  • discard supernatant, carefully resuspend on ice with 10ml cold CaCl2-solution (put a little of the 10ml solution in every falcon before!), pool every resuspended aliquot of one cell line and add 40ml CaCl2-solution (total volume 50ml). Keep 30 min on ice, then centrifuge for 20min; 4°C; 2500g
  • discard supernatant, carefully resuspend pellet in 5,5ml CaCl2(80mM)/Glycerol (4:1), aliquot in Eppis á 60µl and store immediately at - 80 °C


Repeated digestion of PCR product mdnA for cloning into pARW089 (3 fragment ligation)

Investigator: Sabine

Aim: cloning of mdnA and geneIII into pARW089 (3 fragment ligation)

Time: 2011-08-20, 10:00-11:30

Material/Method:

  • 30 µl / 920 ng mdnA
  • 2 µl restriction enzyme NarI
  • 1 µl restriction enzyme AatII
  • 4 µl NEB 10x buffer 4
  • 3 µl water
  • 1 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • ligation into pARW089


Agarose gel electrophoresis of digested mdnA

Investigator: Sabine

Aim: purification of digested DNA fragments

Time: 2011-08-20, 11:30-12:30

Material/Method:

  • digested mdnA
  • 1% agarose gel, loading dye, DNA ladder mix (Fermentas)
  • 100 V

Further Tasks:

  • ligations


Ligation of geneIII and mdnA into pSB1C3

Investigator: Sabine

Time: 2011-08-20, 13:00-16:00

Material/Method:

  • 1 µl mdnA/XbaI+PstI (5,5 ng/µl)
  • 10 µl pSB1C3/XbaI+PstI(17 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 6 µl water
  • 1 h, room temperature


  • 10 µl geneIII/XbaI+PstI (12,2 ng/µl)
  • 1 µl pSB1C3/XbaI+PstI (17 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 6 µl water
  • 1 h, room temperature

Further Tasks:

  • transformation


Ligation of geneIII and mdnA to get a fusion gene

Investigator: Sabine

Time: 2011-08-20, 13:00-16:00

Material/Method:

  • 10 µl mdnA/AgeI (3,8 ng/µl)
  • 5,6 µl geneIII/NgoMIV (15,5 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 1,4 µl water
  • 1 h, room temperature

Further Tasks:

  • digestion with NarI and AatII, ligation into pARW089
  • digestion with XbaI and PstI, ligation into pSB1C3


Ligation of geneIII and mdnA into pARW089 (3 fragment ligation)

Investigator: Sabine

Time: 2011-08-20, 13:00-16:00

Material/Method:

  • 10 µl pARW089/NarI+AatII (60 ng/µl)
  • 1 µl geneIII/NgoMIV+AatII (79 ng/µl)
  • 1,5 µl mdnA/NarI+AgeI (24 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 4,5 µl water
  • 1 h, room temperature

Further Tasks:

  • transformation


Ligation of mdnA into pARW089

Investigator: Sabine

Time: 2011-08-20, 13:00-16:00

Material/Method:

  • 10 µl pARW089/NarI+AatII (60 ng/µl)
  • 1 µl mdnA/NarI+AatII (47 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 6 µl water
  • 1 h, room temperature

Further Tasks:

  • digestion of ligation construct with AgeI and AatII, ligation of geneIII/NgoMIV+AatII (2 step ligation)


71th Labday 2011-08-21

Transformation of competent RV cells with ligation products of pSB1T3/pSB1C3 backbones with Ara, Lac and constitutive promotors

Investigator: Katharina

Idea

  • because of unclear labeling the RV cells used on 2011-08-19 could have been XL1 blue, which already have Tet resistance

Material

  • pSB1T3 clones
    • pSB1T3+YFPI clone b (labeled with "1")
    • pSB1T3+YFPI clone a (labeled with "3")
    • pSB1T3+YFPII plate I clone b (labeled with "4")
  • pSB1C3
  • competent RV cells

Method

  • transformation was done using the heatshock-protocol
  • pSB1T3 clones were plated on LB+agar+Tet
  • pSB1C3 clones were plated on LB+agar+Cm
  • incubation over night at 37°C

Further Tasks

  • pick clones for liquid culture
  • miniprep
  • restriction enzyme digestion for confirmation
  • send for sequencing


miniprep of pSB1T3 clones containing CFP and YFP, respectively

Investigators: Katharina

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 50µl
  • Check concentration with NanoDrop

Results:

  • pSB1T3+YFP I clone b: 690.6 ng/µl
  • pSB1T3+YFP I clone c: 576.3 ng/µl
  • pSB1T3+YFP I clone a: 646.9 ng/µl
  • pSB1T3+YFP II plate 1 clone b: 599.8 ng/µl
  • pSB1T3+YFP II clone a: 562.8 ng/µl
  • pSB1T3+YFP II plate 2 clone d: 569.1 ng/µl
  • pSB1T3+YFP II plate 2 clone c: 415.0 ng/µl
  • pSB1T3+YFP I clone d: 559.9 ng/µl


Digest of pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL

Investigator: Sascha, Sebastian

Aim:

  • Digestion of vector pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL for ligation with AraC and 14_3C protease

Materials:

  • 4 µl of 3 different fractions of pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL (approx. 1,2-1,5 µg DNA)
  • Restriction enzymes BamHI HF and HindIII (purchased form NEB)
  • Buffer 4 (purchased from NEB)

Method:

  • Standard digestion protocol for plasmid DNA

Results:

  • 3 different digested vector fractions of pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL for ligation with AraC and 14_3C protease

Further tasks:

  • purification via gel purification (Kit from Macherey-Nagel)

Output:

  • pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL vector fraction 1, c= ng/ml
  • pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL vector fraction 2, c= ng/ml
  • pJC354_ssTorA_NheI_CS-14_3C_XhoI_blaFL vector fraction 3, c= ng/ml

Assembly PCR of different TEV mutagenesis fraction

Investigator: Sascha, Sebastian

Aim:

  • Assembly of the different fractions of mutated TEV-fragments

Materials:

  • TEV mutagenesis fragment I (fraction I, II, III, IV)
  • TEV mutagenesis fragment II (fraction I, II, III, IV)
  • Primer 1: f_TEV_AraFusion (43)
  • Primer 2: r_TEV_iGEM_BamHI (46)
  • Taq-Polymerase (purchased from Genaxxon)
  • 10x polymerase buffer (purchased from Genaxxon)
  • 10 mM (each) dNTPs (purchased from Genaxxon)
  • double destilled water
  • 25 mM MgCl2

Method:

PCR

  • Template 1: 1µl TEV mutagenesis fragment I (fraction I-IV)
  • Template 2: 1µl TEV mutagenesis fragment II (fraction I-IV)
  • Nucleotides: 1µl of 10mM ready to use dNTP mix
  • 5µl 10x Amplification buffer S
  • 2µl 25mM MgCl2
  • 2,5µl primers = 25pmol absolute (2,5µl of each primer)
  • 33,5µl of pure water
  • 0,5µl TaqPol

Program:

  • Denat: 3min 94°C
  • 5x:

Denat: 45sec 94°C

Anneal:45sec 53°C

Extend:45sec 72°C

  • 25x:

Denat: 45sec 60°C

Anneal:45sec 60°C

Extend:45sec 72°C

  • Final Extend: 10min 72°C

Template batches:

  • TEV mutagenesis fragment I fraction I and TEV mutagenesis fragment II fraction I - fraction 1
  • TEV mutagenesis fragment I fraction I and TEV mutagenesis fragment II fraction II - fraction 2
  • TEV mutagenesis fragment I fraction I and TEV mutagenesis fragment II fraction III - fraction 3
  • TEV mutagenesis fragment I fraction I and TEV mutagenesis fragment II fraction IV - fraction 4
  • TEV mutagenesis fragment I fraction II and TEV mutagenesis fragment II fraction I - fraction 5
  • TEV mutagenesis fragment I fraction II and TEV mutagenesis fragment II fraction II - fraction 6
  • TEV mutagenesis fragment I fraction II and TEV mutagenesis fragment II fraction III - fraction 7
  • TEV mutagenesis fragment I fraction II and TEV mutagenesis fragment II fraction IV - fraction 8
  • TEV mutagenesis fragment I fraction III and TEV mutagenesis fragment II fraction I - fraction 13
  • TEV mutagenesis fragment I fraction III and TEV mutagenesis fragment II fraction II - fraction 14
  • TEV mutagenesis fragment I fraction III and TEV mutagenesis fragment II fraction III - fraction 15
  • TEV mutagenesis fragment I fraction IV and TEV mutagenesis fragment II fraction IV - fraction 16
  • TEV mutagenesis fragment I fraction IV and TEV mutagenesis fragment II fraction I - fraction 9
  • TEV mutagenesis fragment I fraction IV and TEV mutagenesis fragment II fraction II - fraction 10
  • TEV mutagenesis fragment I fraction IV and TEV mutagenesis fragment II fraction III - fraction 11
  • TEV mutagenesis fragment I fraction IV and TEV mutagenesis fragment II fraction IV - fraction 12

Results:

  • 16 different assembled TEV protease fractions with side directed mutagenesis to remove iGEM RS in nucleotide sequence

Further tasks:

  • control of fragments with analytical agarose gelelctrophoresis
  • PCR purification of fractions with the complete assembled TEV-Protease
  • digest of TEV protease fractions with restriction enzymes NgoMIV and PstI and ligation with AraC into the digested (with EcoRI and PstI) vector pUP_SG1_ssTorA_CS-TEV_bla_AraC-TEV
  • transformation of competent E.coli XL1 blue cells with ligated fragments, picking clones, colony PCR, mini-prep of plasmid, sequencing plasmid and survival test with positiv clones

Output:

  • 5 assembled TEV proteases
    • TEV batch 2 c=
    • TEV batch 3 c=
    • TEV batch 7 c=
    • TEV batch 10 c=
    • TEV batch 16 c=

72th Labday 2011-08-22

Elimination of ampicillin resistance in pARW089

Investigators: Nadine, Jessica, Steffi, Nicole

Time: 2011-08-22

Aim:

  • generation of pUP089 from pARW089, vector without ampicillin resistance
  • for mdnA library and later screening

idea:

UP pUP089 plan.jpg

  • digest w/ AvaII and religation


New primer ordered for cloning of geneIII into pARW089 (without mdnA)

Investigators: Sabine

Aim:

  • generation of pARW089 containing only geneIII but not mdnA gene
  • mdnA library could cloned into this vector for screening

Time: 16:00-16:35

Material/Method:

  • Geneious

Result:

  • new forward primer for geneIII containing NarI and NgoMIV restriction site and myc
  • PCR product geneIII can cloned with NarI and AatII into pARWo89

Further tasks:

  • PCR, digestion and ligation


Digestion of mdnA/geneIII fusion gene for cloning into pARW089 (2 step ligation)

Investigator: Sabine

Aim: cloning of mdnA/geneIII fusion gene into pARW089

Time: 2011-08-22, 16:30-17:30

Material/Method:

  • 30 µl / 500 ng mdnA/geneIII
  • 2 µl restriction enzyme NarI
  • 1 µl restriction enzyme AatII
  • 4 µl NEB 10x buffer 4
  • 3 µl water
  • 1 h, 37°C

Further Tasks:

  • ligation into pARW089


Digestion of mdnA/geneIII fusion gene for cloning into pSB1C3 (2 step ligation)

Investigator: Sabine

Aim: cloning of mdnA/geneIII fusion gene into pSB1C3

Time: 2011-08-22, 16:30-17:30

Material/Method:

  • 30 µl / 500 ng geneIII
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme PstI
  • 4 µl NEB 10x buffer 2
  • 4 µl water
  • 0,4 µl BSA
  • 1 h, 37°C

Further Tasks:

  • ligation into pSB1C3


Ligation of mdnA/geneIII into pARW089

Investigator: Sabine

Time: 2011-08-22, 18:00-19:00

Material/Method:

  • 10 µl pARW089/NarI+AatII (60 ng/µl)
  • 8 µl mdnA/geneIII (16 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 1 h, room temperature

Further Tasks:

  • transformation


Ligation of mdnA/geneIII into pSB1C3

Investigator: Sabine

Time: 2011-08-22, 18:00-19:00

Material/Method:

  • 8 µl pARW089/NarI+AatII (60 ng/µl)
  • 9 µl mdnA/geneIII (16 ng/µl)
  • 2 µl 10x T4 ligase buffer
  • 1 µl T4 ligase
  • 1 h, room temperature

Further Tasks:

  • transformation


Transformation of generated vector constructs in E. coli

Investigators: Sabine

Aim: amplification and control of generated vectors

  • mdnA, geneIII or mdnA/geneIII in pSB1C3
  • mdnA or mdnA/geneIII in pARW089

Time: 20:30-22:00

Method:

  • addition of 4 µl ligation reaction to XL1-blue cells
  • incubation 15 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 2 min on ice
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates containing 100 µg/ml kanamycin (pARW089) or chloramphenicol (pPSB1C3)
  • storage over night at 37°C

Further tasks:
control cell clones


Digest of pSB1C3, pSB1T3 clones containing CFP and YFP, respectively as well as PCR products of promoters

Investigators: Jessica

Time: 2011-08-22

Materials

  • pSB1C3 (BBa_K40304_Affibody_MiddleLinker) from
  • pSB1T3+YFP I clone b and pSB1T3+YFP II clone a from 2011-08-21 (Katharina)
  • PCR fragments: Arabinose, IPTG-inducible, constitutive

Method:

  • Reaction mix:
pSB1C3 pSB1T3+YFP I clone b pSB1T3+YFP II clone a PCR fragments
DNA 6 3 3 20
10x Buffer 4 NEB 2 2 2 3
XbaI 1 1 1 1
EcoRI 1 1 1 1
100x BSA 0.2 0.2 0.20.3
H2O 9.8 12.8 12.84.8
total 20 20 2030
  • at 37°C for approx. 3 h
  • heat inactivation at 65°C for 20 min

Agarose gel

Gel extraction:

  • using Promega- Wizard SV Gel and PCR Clean Up System
  • elute in 30 µl nuclease-free water

Dephosphorylation of pSB1C3:

  • using Promega TSAP
  • adding 3 µl Buffer and 1 µl TSAP
  • incubate at 37°C for 15 min
  • heat inactivaton at 74°C for 15 min

Results:


73th Labday 2011-08-23

overnight culture of picked E. coli clones transformed with pPDV

Investigators: Sabine

Aim: amplification and purification of generated phage display vector pPDV089 for test digestion and sequencing

Time: 11:00-13.00

Method/Materials:

  • 10 clones pARW089+mdnA/geneIII from 3 ragment ligation
  • 10 clones pARW089+mdnA/geneIII from 2 step ligation
  • 5 clones pARW089+mdnA
  • 5 clones pSB1C3+mdnA
  • 5 clones pSB1C3+geneIII
  • 5 clones pSB1C3+mdnAIgeneIII
  • 5 ml LB medium per clone containining 25 µg/ml chloramphenicol (pSB1C3) or kanamycin (pARW089)
  • storage over night at 37°C and 800 rpm

Further tasks:

plasmid preparation, test digestion and sequencing

PCR: BioBrick mdnABC, mdnC, mdnE, mdnDE, mdnBC

Time: 2011-08-23, 8:00-11:30

Investigators: Nadine, Nicole

Materials

  • vector: pARW089, 20.8.11, 333.4 ng/µl
  • Phusion HF Polymerase, NEB
  • Phusion HF Buffer
  • dNTPs
  • water
  • Primer:
# Primer
57 pf_mdnABC_EcoRI_NotI_XbaI 12.08.
58 pf_mdnB_EcoRI_NotI_XbaI 12.08.
59 pf_mdnC_EcoRI_NotI_XbaI 12.08.
60 pf_mdnD_EcoRI_NotI_XbaI 12.08.
61 pf_mdnE_EcoRI_NotI_XbaI 12.08.
62 pr_mdnABC_SpeI_NotI_PstI 12.08.
63 pr_mdnB_SpeI_NotI_PstI 12.08.
64 pr_mdnD_SpeI_NotI_PstI 12.08.
65 pr_mdnE_SpeI_NotI_PstI 12.08.

Protocol:

  • Reaction mix
    • 2 µl pARW089 (diluted 1:100)
    • 1 µl dNTPs (10 mM)
    • 2.5 µl Primer forward (10 mM)
    • 2.5 µl Primer backward (10 mM)
    • 10 µl Buffer (5x)
    • 0.5 µl Phusion HF Ploymerase (2U/µl)
    • 31.5 µl water
    • total volume: 50 µl
  • Master mix
    • 12 µl pARW089 (diluted 1:100)
    • 6 µl dNTPs (10 mM)
    • 60 µl Buffer (5x)
    • 3 µl Phusion HF Ploymerase (2U/µl)
    • 189 µl water
  • Primer
    • mdnABC: 57, 62
    • mdnC: 59, 62
    • mdnE: 61, 65
    • mdnDE: 61, 64
    • mdnBC: 58, 62

2. PCR programs

  • IGBIO02 for mdnABC, mdnC
  • first steps: 10x
  • second steps: 20x
Step Temperature Time
Hot Start 98°C Hold
Initial denaturation 98°C 30 sec
Denaturation 98°C 10 s
Annealing 59°C 30 s
Extension 72°C 20 s
DenaturationII 98°C 10 s
AnnealingII 72°C 30 s
ExtensionII 72°C 20 s
Final extension 72°C 10 min
  • IGBIO03 for mdnE, mdnDE, mdnBC
  • first steps: 10x
  • second steps: 20x
Step Temperature Time
Hot Start 98°C Hold
Initial denaturation 98°C 30 sec
Denaturation 98°C 10 s
Annealing 52°C 30 s
Extension 72°C 60 s
DenaturationII 98°C 10 s
AnnealingII 72°C 30 s
ExtensionII 72°C 60 s
Final extension 72°C 10 min

Results:

  • Output:
      • mdnABC, Nad & Nic, 23.8.11
      • mdnC, Nad & Nic, 23.8.11
      • mdnE, Nad & Nic, 23.8.11
      • mdnDE, Nad & Nic, 23.8.11
      • mdnBC, Nad & Nic, 23.8.11


Digest of pSB1T3+YFPI/II vectors for ligation w/ promotors

Time: 2011-08-23, 9:00-

Investigators: Nadine, Nicole, Katharina

Materials

  • vectors from 2011-08-21 (Katharina):
    • pSB1T3+YFP I clone b: 690.6 ng/µl
    • pSB1T3+YFP I clone c: 576.3 ng/µl
    • pSB1T3+YFP I clone a: 646.9 ng/µl
    • pSB1T3+YFP II plate 1 clone b: 599.8 ng/µl
    • pSB1T3+YFP II clone a: 562.8 ng/µl
    • pSB1T3+YFP II plate 2 clone d: 569.1 ng/µl
    • pSB1T3+YFP II plate 2 clone c: 415.0 ng/µl
    • pSB1T3+YFP I clone d: 559.9 ng/µl
  • EcoRI HF
  • XbaI
  • BSA (10x)
  • Buffer 4
  • water

Protocol:

  • Reaction mix
    • 2 µl DNA
    • 1 µl EcoRI
    • 1 µl XbaI
    • 0.3 µl BSA
    • 3 µl Buffer 4 (10x)
    • 22.7 µl water
    • total volume: 30 µl
  • incubation at 37°C for 2 hrs

Agarose gel

Investigator: Jessica

  • Gel extraction using NucleoSpin ExtractII (Macherey-Nagel)
    • no excision of pSB1T3+YFP II plate 2 clone c because of no visible band

Results:


Digest of amplified 14_3C protease (assembled fragments after sidedirected mutagenesis), amplified AraC (from pBAD_iGEM_express mVenus), plasmid pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL and plasmid pJC354_ssTorA_XhoI_CS-TEV_NheI_blaFL

Investigator: Sebastian, Sascha

Material:

  • Restriction enzymes NgoMIV, HindIII, BamHI, PstI-HF, EcoRI-HF (purchased from NEB)
  • digest buffer 2 and 4 (puchased from NEB)
  • BSA (purchased from NEB)
  • plasmid pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL
  • plasmid pJC354_ssTorA_XhoI_CS-TEV_NheI_blaFL
  • PCR amplified AraC-fragment
  • PCR amplified and mutated 14_3C protease

Methode:

Standard protocoll for DNA digest.

Reaction batches:

  • Batch 1: 21.7 µl 14_3C fraction I (c=157.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl BamHI, 0.3 µl BSA, 3 µl Buffer 4
  • Batch 2: 21.7 µl 14_3C fraction II(c=157.5 ng/µl), 2.5 µl NgoMIV, 2.5 µl BamHI, 0.3 µl BSA, 3 µl Buffer 4
  • Batch 3: 22.0 µl AraC (c=175.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl HindIII, 3 µl Buffer 2
  • Batch 4: 22.0 µl AraC (c=175.0 ng/µl), 2.5 µl NgoMIV, 2.5 µl EcoRI-HF, 3 µl Buffer 4
  • Batch 5: 6,9 µl plasmid pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL II (c= ng/µl), 1.0 µl HindIII, 2.5 µl BamHI, 0.1 µl BSA, 1 µl Buffer 2
  • Batch 6: 6,9 µl plasmid pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL VII (c= ng/µl), 1.0 µl HindIII, 2.5 µl BamHI, 0.1 µl BSA, 1 µl Buffer 2
  • Batch 7: 7.0 µl plasmid pJC354_ssTorA_XhoI_CS-TEV_NheI_blaFL (c= ng/µl), 1.0 µl EcoRI-HF, 1.0 µl PstI-HF, 1.0 µl Buffer 4

Further tasks:

All plasmid fractions should be purified with 1.0% agarose gel, all other fragments with 1.5% agarose gel and extracted with Macherey-Nagel Nucleo SpinII Kit.

  • Ligation of fragments in different combinations and transformation of competent E.coli XL1 blue cells.

Output:

  • digested fragments of AraC, 14_3C protease and plasmid backbones for transformation (AraC + 14_3C + "14_3C-backbone", AraC + TEV + "TEV-backbone")

1) EcoRI_AraC_NgoMIV

2) HindIII_AraC_NgoMIV

3) NgoMIV_14_3C_BamHI Batch 1

4) NgoMIV_14_3C_BamHI Batch 2

5) BamHI_pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL_HindIII Batch 1

6) BamHI_pJC354_ssTorA_XhoI_CS-143C_NheI_blaFL_HindIII Batch 2

7) BamHI_pJC354_ssTorA_XhoI_CS-TEV_NheI_blaFL_HindIII

Agarose Gel of PCR products for BioBricks mdnABC, mdnBC, mdnC, mdnC, mdnD, mdnDE, mdnE and PCR purification

Investigators: Nadine, Nicole, Katharina, Jessica

Time: 2011-08-23, 13:00-16:00

Materials:

  • PCR products
  • Agarose broad range (Roth)
  • 1x TAE buffer
  • Gel Red
  • DNA Ladder Mix (Fermentas)
  • 6x Loading Dye (Fermentas)

Production of one 1 % agarose gel

  • 2 x 1 % gel: 0.5 g agarose in 50 ml 1x TAE buffer
  • Adding 2 µl gel red to each gel

Loading gels and running

  • Add µl Loading dye to each 2 µl sample
  • 12 µl DNA Ladder Mix
  • Running conditions: 110 V, approx. 45 min

Loading of gel

lane Sample Volume in µl Expected size in bp
M marker 12
1 mdnABC - 2492
2 mdnB - 1021
3 mdnBC - 2045
4 mdnC - 1007
5 mdnD - 600
6 mdnDE - 2800
7 mdnE - 2100

Result gel 1:

UP PCR biobrick mdnABCDE 2011-08-23.jpg

  • all PCR products appear as expected, except mdnB
  • purification of PCR products w/ Machery and Nagel PCR purification kit
  • Output:
    • PCR pur., mdnABC, 48.1 ng/µl, Kat, 23.8.11
    • PCR pur., mdnBC, 70.1 ng/µl, Kat, 23.8.11
    • PCR pur., mdnC, 62 ng/µl, Kat, 23.8.11
    • PCR pur., mdnD, 67.1 ng/µl, Kat, 23.8.11
    • PCR pur., mdnDE, 61.8 ng/µl, Kat, 23.8.11
    • PCR pur., mdnE, 68.7 ng/µl, Kat, 23.8.11

Further task:

  • repeat PCR for mdnB
  • digestion of other PCR products
  • ligation w/ pSB1C3


Test digest of pSB1A3+CFP/YFP and pSB1K3+CFP/YFP vectors w/ promotors

Investigators: Steffi, Nadine, Nicole

Materials

  • vectors from 2011-08-20 (Katharina):
    • pSB1A3-CFP +Ara (clone A) 12: 342.1 ng/µl
    • pSB1A3-CFP +Ara (clone B) 7: 252.5 ng/µl
    • pSB1A3-CFP +Ara (clone C) 6: 356.9 ng/µl
    • pSB1A3-YFP +Ara (clone A) 1: 339.2 ng/µl
    • pSB1A3-YFP +Ara (clone B) 5: 379.0 ng/µl
    • pSB1A3-YFP +Ara (clone C) 14: 221.4 ng/µl
    • pSB1A3-CFP +Lac (clone A) 15: 319.3 ng/µl
    • pSB1A3-CFP +Lac (clone B) 34: 105.5 ng/µl
    • pSB1A3-CFP +Lac (clone C) 33: 135.7 ng/µl
    • pSB1A3-YFP +Lac (clone A) 16: 110.6 ng/µl
    • pSB1A3-YFP +Lac (clone B) 4: 340.4 ng/µl
    • pSB1A3-YFP +Lac (clone C) 13: 290.6 ng/µl
    • pSB1A3-CFP + const (clone A) 11: 312.2 ng/µl
    • pSB1A3-CFP + const (clone B) 9: 218.0 ng/µl
    • pSB1A3-CFP + const (clone C) 10: 201.7 ng/µl
    • pSB1A3-YFP + const (clone C) 28: 238.0 ng/µl
    • pSB1K3-CFP +Ara (clone A) 25: 175.2 ng/µl
    • pSB1K3-CFP +Ara (clone B) 31: 190.2 ng/µl
    • pSB1K3-CFP +Ara (clone C) 24: 193.8 ng/µl
    • pSB1K3-YFP +Ara (clone A) 22: 119.6 ng/µl
    • pSB1K3-YFP +Ara (clone B) 19: 149.4 ng/µl
    • pSB1K3-YFP +Ara (clone C) 30: 135.1 ng/µl
    • pSB1K3-CFP +Lac (clone A) 20: 138.4 ng/µl
    • pSB1K3-CFP +Lac (clone B) 21: 58.3 ng/µl
    • pSB1K3-CFP +Lac (clone C) 23: 122.0 ng/µl
    • pSB1K3-YFP +Lac (clone A) 29: 69.3 ng/µl
    • pSB1K3-YFP +Lac (clone B) 17: 153.1 ng/µl
    • pSB1K3-YFP +Lac (clone C) 18: 90.9 ng/µl
    • pSB1K3-CFP + const (clone A) 26: 89.8 ng/µl
    • pSB1K3-CFP +const (clone B) 8: 252.5 ng/µl
    • pSB1K3-CFP +const (clone C) 2: 256.6 ng/µl
    • pSB1K3-YFP + const (clone A) 27: 55.7 ng/µl
    • pSB1K3-YFP +const (clone B) 3: 231.9 ng/µl
    • pSB1K3-YFP + const (clone C) 32: 174.9 ng/µl
  • BamHI
  • AatII
  • HpaI
  • HincII
  • NotI
  • BSA (10x)
  • Buffer 3
  • Buffer 4
  • water

Protocol:

  • Reaction mix (Arabinose)
    • 0.5 µl DNA
    • 1 µl BamHI
    • 1 µl AatII
    • 0.3 µl BSA
    • 3 µl Buffer 4 (10x)
    • 24.2 µl water
  • Reaction mix (Lac)
    • 0.5 µl DNA
    • 1 µl HpaI
    • 1 µl AatII
    • 3 µl Buffer 4 (10x)
    • 24.5 µl water
  • Reaction mix (constitutive)
    • 0.5 µl DNA
    • 1 µl HincII
    • 1 µl NotI
    • 0.3 µl BSA
    • 3 µl Buffer 3 (10x)
    • 24.2 µl water
    • total volume each: 30 µl
  • incubation at 37°C for 1 hrs

further tasks:

  • gel electrophoresis
  • ligation
  • transformation


Agarose Gel of pSB1A3+CFP/YFP and pSB1K3+CFP/YFP

Investigators: Steffi, Katharina, Nadine

Materials:

  • digestion products
  • Agarose broad range (Roth)
  • 1x TAE buffer
  • Gel Red
  • DNA Ladder Mix (Fermentas)
  • 6x Loading Dye (Fermentas)

Production of one 1 % agarose gel

  • 1 x 1 % gel: 1,0 g agarose in 100 ml 1x TAE buffer
  • Adding 4 µl gel red to gel

Loading gels and running

  • Add 5 µl Loading dye to each 2 µl sample
  • 7 µl DNA Ladder Mix
  • Running conditions: 110 V, approx. 45 min

Loading of gel

lane Sample Volume in µl Expected size in bp
M marker 7
1 pSB1A3-CFP +Ara (clone A) 15
2 pSB1A3-CFP +Ara (clone B) 15
3 pSB1A3-CFP +Ara (clone C) 15
4 pSB1A3-YFP +Ara (clone A) 15
5 pSB1A3-YFP +Ara (clone B) 15
6 pSB1A3-YFP +Ara (clone C) 15
7 pSB1K3-CFP +Ara (clone A) 15
8 pSB1K3-CFP +Ara (clone B) 15
9 pSB1K3-CFP +Ara (clone C) 15
10 pSB1K3-YFP +Ara (clone A) 15
11 pSB1K3-YFP +Ara (clone B) 15
12 pSB1K3-YFP +Ara (clone C) 15
M marker 7
13 pSB1A3-CFP + const (clone A) 15
14 pSB1A3-CFP + const (clone B) 15
15 pSB1A3-CFP + const (clone C) 15
16 pSB1A3-YFP + const (clone C) 15
17 pSB1K3-CFP + const (clone A) 15
18 pSB1K3-CFP + const (clone B) 15
19 pSB1K3-CFP + const (clone C) 15
20 pSB1K3-YFP + const (clone A) 15
21 pSB1K3-YFP + const (clone B) 15
22 pSB1K3-YFP + const (clone C) 15
M marker 7
23 pSB1A3-CFP +Lac (clone A) 15
24 pSB1A3-CFP +Lac (clone B) 15
25 pSB1A3-CFP +Lac (clone C) 15
26 pSB1A3-YFP +Lac (clone A) 15
27 pSB1A3-YFP +Lac (clone B) 15
28 pSB1A3-YFP +Lac (clone C) 15
29 pSB1K3-CFP +Lac (clone A) 15
30 pSB1K3-CFP +Lac (clone B) 15
31 pSB1K3-CFP +Lac (clone C) 15
32 pSB1K3-YFP +Lac (clone A) 15
33 pSB1K3-YFP +Lac (clone B) 15
34 pSB1K3-YFP +Lac (clone C) 15

Result gel:

UP AG A3K3 CFPYFP+Promotor Digest 2011-08-23.JPG

  • sample ... used for sequencing

further tasks:

  • sequencing


Agarose Gel of pARW089 Ava II A (3µl DNA)/ B (4µl DNA) (= pUP089)

Investigators: Niels, Nadja

Materials:

  • digestion products
  • Agarose broad range (Roth)
  • 1x TAE buffer
  • Gel Red
  • DNA Ladder Mix (Fermentas)
  • 6x Loading Dye (Fermentas)

Production of one 0,8 % agarose gel

  • 1 x 0,8 % gel: 0,4 g agarose in 50ml 1x TAE buffer
  • Adding 2 µl gel red to gel

Loading gels and running

  • Add 6 µl Loading dye to each 30 µl sample
  • 20 µl DNA Ladder Mix 1:10 diluted
  • Running conditions: 100 V, approx. 50 min

Loading of gel

lane Sample Volume in µl Expected size in bp
M marker 20
1 pARW089 Ava II A 36 over 10kbp
2 pARW089 Ava II B (4µl DNA) 36 over 10kbp

Result gel:

  • sample used for gel extraction (Promega Kit Wizard SV Gel and PCR Clean Up System)
  • sample used for ligation

Further tasks:

  • transformation


Ligation of pSB1C3 and pSB1T3-YFPI/II with promoters and ligation of pARW089 AvaII

Investigators: Jessica

Materials:

  • T4 Ligase (Promega)
  • 10x T4 Ligase Buffer (Promega)
  • digested, gel purified, dephoshorylated vectors: pSB1C3, pSB1T3-YFP I clone c, pSB1T3-YFP II plate 2 clone d
  • Inserts: Ara promoter, Lac promoter, constitutive promoter

Method:

  • 10 µl reaction for pSB vectors:
    • 1 µl 10x T4 Ligase Buffer
    • 1 µl T4 Ligase
    • 6 µl vector
    • 2 µl insert
  • 10 µl reaction for pARW089 vector:
    • 1 µl 10x T4 Ligase Buffer
    • 1 µl T4 Ligase
    • 8 µl vector
  • at 14°C overnight

Results:

  • 14 ligation products
    • pSB1C3 + Ara
    • pSB1C3 + Lac
    • pSB1C3 + const
    • pSB1C3 + H2O
    • pSB1T3-YFP II + Ara
    • pSB1T3-YFP II + Lac
    • pSB1T3-YFP II + const
    • pSB1T3-YFP II + H2O
    • pSB1T3-YFP I + Ara
    • pSB1T3-YFP I + Lac
    • pSB1T3-YFP I + const
    • pSB1T3-YFP I + H2O
    • pARW089 AvaII A = pUP089 A
    • pARW089 AvaII B = pUP089 B

Further tasks:

  • transformation


Over night culture of several pSB1A3+CFP/YFP and pSB1K3+CFP/YFP with promotor

Time: 2011-08-23, 18:00-22:30

Investigators: Niels, Jessica, Nadja

Materials

  • 5 ml LB media
  • 5 µl antibotic (KAN/AMP - Stock)
  • clone
    • KAN YFP ava clone IV (from plate)
    • KAN YFP ava clone V (from plate)
    • KAN YFP ava clone VI (from plate)
    • KAN CFP const clone I (from pre-culture)
    • KAN CFP const clone II (from pre-culture)
    • KAN CFP const clone III (from pre-culture)
    • KAN YFP const clone I (from pre-culture)
    • KAN YFP const clone II (from pre-culture)
    • KAN YFP const clone III (from pre-culture)
    • AMP CFP const clone I (from pre-culture)
    • AMP CFP const clone II (from pre-culture)
    • AMP CFP const clone III (from pre-culture)
    • AMP YFP const clone I (from pre-culture)

conditions

  • 37 °C
  • 250 rpm
  • over night

further tasks:

  • miniprep
  • digest
  • analytic gel


sequencing of

Time: 2011-08-23, 18:00-22:30

Investigators: Nadja ,Niels ,Jessica

Materials

Sequencing by eurofins mwg|operon

Label - Barcode

  • 1cB - AKM001W053
  • 1cC - AKM001W054
  • 1cA - AKM001W055
  • 2cB - AKM001W056
  • 2cA - AKM001W057
  • 2cD - AKM001W058
  • 2cC - AKM001W059
  • 1cD - AKM001W060


sequencing of

Time: 2011-08-23, 18:00-22:30

Investigators: Nadja ,Niels ,Jessica

Materials

Sequencing by eurofins mwg|operon

Label - Barcode

  • K3CAcA - AKM001W061
  • A3CAcA - AKM001W062
  • A3YAcA - AKM001W063
  • K3YIcC - AKM001W064
  • K3CIcB - AKM001W065
  • A3YIcB - AKM001W066
  • A3cIcA - AKM001W067


over night culture

Time: 2011-08-23, 18:00-22:30

Investigators: Niels, Jessica, Nadja

Materials

  • 5 ml LB Media
  • 5 µl Amp/Kan
  • clones
    • pSBA3-YFP+const
    • pSBA3-CFP+const A
    • pSBA3-CFP+const C
    • pSBK3-YFP+const A
    • pSBK3-CFP+const A
    • pSBK3-YFP+ara V

overnight 37°C

further tasks:

  • miniprep


74th Labday 2011-08-24

Transformation w/ pUP089 A and B, BBa_K40304_Affibody_MiddleLinker+Ara/Const/Lac, pSB1T3+YFPI+Ara/Const/Lac and pSB1T3+YFPII+Ara/Const/Lac

Investigators: Nicole, Nadine

Time: 7:00-9:00

Aim:

  • creating pARW089 without Amp resistance, called then pUP089
  • get expression backbones w/ Tet or Cm resistance and Ara, Const. or Lac promotors

Material:

  • XL1-blue (competent)
  • RV-308 (competent)
  • ligation products from o.n. ligation from 2011-08-23 (Jessica)
    • pSB1C3 + Ara
    • pSB1C3 + Lac
    • pSB1C3 + const
    • pSB1C3 + H2O
    • pSB1T3-YFP II + Ara
    • pSB1T3-YFP II + Lac
    • pSB1T3-YFP II + const
    • pSB1T3-YFP II + H2O
    • pSB1T3-YFP I + Ara
    • pSB1T3-YFP I + Lac
    • pSB1T3-YFP I + const
    • pSB1T3-YFP I + H2O
    • pARW089 AvaII A = pUP089 A
    • pARW089 AvaII B = pUP089 B
  • for pSB1T3 plasmids RV-308 cells were used
  • for others: Xl1-blue
  • LB-Agar
  • tetracycline
  • chloramphenicol
  • kanamycine

Method:

  • addition of 2 µl ligation reaction to XL1-blue cells
  • incubation 60 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates:
    • pUP089
      • 100 µg/ml ampicilin
      • 100 µg/ml kanamycin
      • 100 µg/ml ampicilin and kanamycin
    • pSB1T3
      • 100 µg/ml tetracyclin
    • pSB1C3
      • 100 µg/ml chloramphenicol
  • incubation for 20 hrs at 37°C

Further tasks:
control cell clones


Miniprep of E.coli overnight culture containing created pPDV089

Investigators: Sabine, Laura

Aim: purification of pPDV089 for test digestion and sequencing

Time: 10:00-15:00

Method/Materials:

  • see protocol 5.1 of the NucleoSpin Plasmid Kit
  • 5 clones containing pSB1C3+mdnA
  • 5 clones containing pSB1C3-geneIII
  • 5 clones containing pSB1C3-mdnA/geneIII
  • 10 clones containing pARW089+mdnA
  • 10 clones containing pARW089+mdnA/geneIII (3 fragment ligation)
  • 10 clones containing pARW089+mdnA/geneIII (2 step ligation)

Further tasks: test digestion

Test digestion of purified plasmids pARW089

Investigators: Sabine

Aim:control of liagation of mdnA and geneIII into pARW089

Time: 13:00-17:00

Materials/Methods:

  • 0,5 µl XbaI
  • 0,5 µl SpeI
  • 2 µl 10x buffer 4 (NEB)
  • 0,2 µl BSA
  • 2 µl vector DNA (ca. 1 µg)
  • 14,8 µl water
  • incubate for 3 h at 37°C

Results:

  • expected band sizes for pARW089 containing mdnA and geneIII: ca. 5300 bp, 4500 bp, 630 bp and 90
  • expected band sizes for pARW089 not containing the inserts: ca. 10000 bp, 630 bp and 90 bp


Test digestion of purified plasmids pSB1C3

Investigators: Sabine

Aim:control of liagation of geneIII, mdnA and mdnA/geneIII into pSB1C3

Time: 18:00-18:30

Materials/Methods:

  • per reaction:
  • 0,5 µl XbaI
  • 0,5 µl PvuI
  • 2 µl 10x buffer 3 (NEB)
  • 0,2 µl BSA
  • 5 µl vector DNA (ca. 1 µg)
  • 11,8 µl water
  • incubate over night at 37°C

Results:

Agarose gel electrophoresis of digested mdn fragments and pSB1C3, gel extraction and ligation

Investigators: Nicole, Jessica, Steffi, Niels

Time: 2011-08-24,

Materials

  • digests of :
    • mdnB
    • mdnC
    • mdnD
    • mdnE
    • mdnBC
    • mdnDE
    • mdnABC
    • pSB1C3
  • agarose, 1x TAE, gel red
  • gel extraction kit (Promega)
  • thermosensitive alkaline phoshatase (TSAP, Promega)
  • ligase

Gel electrophoresis:

  • 1,25% agarose gel (0.625 g agarose + 50 ml 1x TAE, 2 µl gel red)
  • 30 µl digest + 6 µl 6x loading dye

Gel 1

lane Sample Volume in µl Expected size in bp
1 mdnB 15 ~1021
2 mdnB 15 ~1021
3 mdnC 15 ~1007
4 mdnC 15 ~1007
5 mdnD 15 ~600
6 mdnD 15 ~600
M GeneRuler™ DNA Ladder Mix (diluted 1:10) 10

UP AG digest mdn genes 1 2011-08-24 Jessica.jpg

Gel 2

lane Sample Volume in µl Expected size in bp
1 mdnE 36 ~2100
2 mdnBC 36 ~2045
3 mdnDE 36 ~2800
4 mdnABC 36 ~2492
5 -
6 pSB1C3 36 ~2389, 243

UP AG digest mdn genes 2 2011-08-24 Jessica.jpg

Gel extraction:

  • using Promega- Wizard SV Gel and PCR Clean Up System

Dephosphorylation of pSB1C3:

  • using Promega TSAP
    • adding 5 µl Buffer and 1 µl TSAP
    • incubate at 37°C for 15 min
    • heat inactivaton at 74°C for 15 min

Nanodrop

sample c [ng/µl] 260nm/280nm 260nm/230nm
mdnB 10,2 2,08 0,57
mdnC 13,4 2,3 0,4
mdnD 11,8 1,94 0,4
mdnE 13,3 1,93 0,78
mdnBC 16,3 1,91 0,79
mdnDE 13,8 1,92 0,60
mdnABC 13,4 1,89 0,68
C3 44,4 1,90 1,45

Ligation:

Insert [µl] Vector [µl]
mdnB 6 C3 2
mdnC 6 C3 2
mdnD 7 C3 1
mdnE 5 C3 3
mdnBC 5 C3 3
mdnDE 5 C3 3
mdnABC 5 C3 3
  • 1 µl 10x Buffer
  • 1 µl T4 Ligase
    • over night by 14°C

further tasks:

  • transformation


Digest of pSB1A3+CFP/YFP and pSB1K3+CFP/YFP vectors w/ promotors

Investigators: Jessica, Nadja

Time: 2011-08-24, 14:00-20:00

Materials

  • vectors from 2011-08-24:
    • pSB1A3-CFP + const (clone A)
    • pSB1A3-CFP + const (clone B)
    • pSB1A3-CFP + const (clone C)
    • pSB1A3-YFP + const (clone C)
    • pSB1K3-YFP +Ara (clone V)
    • pSB1K3-YFP +Ara (clone V box)
    • pSB1K3-YFP +Ara (clone VI)
    • pSB1K3-CFP + const (clone A)
    • pSB1K3-CFP +const (clone B)
    • pSB1K3-CFP +const (clone C)
    • pSB1K3-YFP + const (clone A)
    • pSB1K3-YFP +const (clone B)
    • pSB1K3-YFP + const (clone C)
  • NdeI
  • NruI
  • HincII
  • NotI
  • BSA (100x)
  • Buffer 3
  • water

Digest:

  • Reaction mix (Arabinose)
    • 0.5 µl DNA
    • 0.5 µl NdeI
    • 0.5 µl NruI
    • 2 µl Buffer 3 (10x)
    • 16.5 µl water
  • Reaction mix (constitutive)
    • 0.5 µl DNA
    • 0.5 µl HincII
    • 0.5 µl NotI
    • 0.2 µl BSA
    • 2 µl Buffer 3 (10x)
    • 16.3 µl water
  • total volume each: 20 µl
  • incubation at 37°C for 1.5 hrs

Gel electrophoresis:

  • 1% agarose gel (0.5 g agarose + 50 ml 1x TAE, 2 µl gel red)
  • 20 µl digest + 4 µl 6x loading dye

Gel 1

lane Sample Volume in µl Expected size in bp
M GeneRuler™ DNA Ladder Mix (diluted 1:10) 20
1 pSB1A3-CFP + const (clone A) (undigested) 6
2 pSB1A3-CFP + const (clone A) 15 2145, 804
3 pSB1A3-CFP + const (clone B) 15 2145, 804
4 pSB1A3-CFP + const (clone C) 15 2145, 804
5 pSB1A3-YFP + const (clone C) 15 2145, 804
6 -
7 pSB1K3-YFP +Ara (clone V) undigested 6
8 pSB1K3-YFP +Ara (clone V) 15 ~ 2800, 870, 430
9 pSB1K3-YFP +Ara (clone V box) 15 ~ 2800, 870, 430
10 pSB1K3-YFP +Ara (clone VI) 15 ~ 2800, 870, 430

UP AG digest pSB-prom 1 2011-08-24 Jessica.jpg

Gel 2

lane Sample Volume in µl Expected size in bp
M GeneRuler™ DNA Ladder Mix (diluted 1:10) 20
1 -
2 pSB1K3-CFP + const (clone A) 15 2145, 804
3 pSB1K3-CFP +const (clone B) 15 2145, 804
4 pSB1K3-CFP +const (clone C) 15 2145, 804
5 pSB1K3-YFP + const (clone A) 15 2145, 804
6 pSB1K3-YFP +const (clone B) 15 2145, 804
7 pSB1K3-YFP + const (clone C) 15 2145, 804
8 pSB1K3-CFP + const (clone A) undigested 6

UP AG digest pSB-prom 2 2011-08-24 Jessica.jpg

further tasks:

  • repeat digest of pSB1K3 + const with more DNA
  • have a look at digest of pSB1K3 + Ara


Transformation w/ pUP089 A and B, BBa_K40304_Affibody_MiddleLinker+Ara/Const/Lac, pSB1T3+YFPI+Ara/Const/Lac and pSB1T3+YFPII+Ara/Const/Lac

Investigators: Nicole, Nadine

Time: 7:00-9:00

Aim:

  • creating pARW089 without Amp resistance, called then pUP089
  • get expression backbones w/ Tet or Cm resistance and Ara, Const. or Lac promotors

Material:

  • XL1-blue (competent)
  • RV-308 (competent)
  • ligation products from o.n. ligation from 2011-08-23 (Jessica)
    • pSB1C3 + Ara
    • pSB1C3 + Lac
    • pSB1C3 + const
    • pSB1C3 + H2O
    • pSB1T3-YFP II + Ara
    • pSB1T3-YFP II + Lac
    • pSB1T3-YFP II + const
    • pSB1T3-YFP II + H2O
    • pSB1T3-YFP I + Ara
    • pSB1T3-YFP I + Lac
    • pSB1T3-YFP I + const
    • pSB1T3-YFP I + H2O
    • pARW089 AvaII A = pUP089 A
    • pARW089 AvaII B = pUP089 B
  • for pSB1T3 plasmids RV-308 cells were used
  • for others: Xl1-blue
  • LB-Agar
  • tetracycline
  • chloramphenicol
  • kanamycine

Method:

  • addition of 2 µl ligation reaction to XL1-blue cells
  • incubation 60 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates:
    • pUP089
      • 100 µg/ml ampicilin
      • 100 µg/ml kanamycin
      • 100 µg/ml ampicilin and kanamycin
    • pSB1T3
      • 100 µg/ml tetracyclin
    • pSB1C3
      • 100 µg/ml chloramphenicol
  • incubation for 20 hrs at 37°C

Further tasks:
control cell clones


Miniprep of o. n. culture of pSB1K3 constitutive and Ara as well as pSB1A3 constitutive and Ara

Time: 7:00-

Investigators: Nicole, Nadine, Nadja

Results:


Concentration:

  • pSBA3-YFP+const C = 470,8 ng/µl
  • pSBA3-CFP+const A = 889,2 ng/µl
  • pSBA3-CFP+const C = 692,8 ng/µl
  • pSBK3-YFP+const A = 495,0 ng/µl
  • pSBK3-CFP+const A = 1142,0 ng/µl
  • pSBK3-YFP+ara V = 380,1 ng/µl

Further task:

  • sequencing


75th Labday 2011-08-25

check plates from transformation (expression backbones in XL1-blue, 2011-08-24)

Time: 7:00-7:20

Investigators: Nicole, Nadine

Aim:

  • build expression backbones w/ different promotors

Material:

  • on chloramphenicol plates (in XL1 blue)
    • pSB1C3 + Ara
    • pSB1C3 + Lac
    • pSB1C3 + const
    • pSB1C3 + H2O
    • pSB1T3-YFP II + Ara
    • pSB1T3-YFP II + Lac
    • pSB1T3-YFP II + const
    • pSB1T3-YFP II + H2O
    • pSB1T3-YFP I + Ara
    • pSB1T3-YFP I + Lac
    • pSB1T3-YFP I + const
    • pSB1T3-YFP I + H2O

Results:

  • buffer control was over grown

conclusions:

  • something is wrong with competent cells

Further tasks:

  • check competent cells


check plates from transformation (pUP089 in XL1-blue, 2011-08-24)

Time: 7:00-7:20

Investigators: Nicole, Nadine

Aim:

  • creating pARW089 without Amp resistance, called then pUP089

Material:

  • pUP089 A in XL1 blue
  • pUP089 B in XL1 blue
  • on kan, amp or kan and amp plates

Results:

UP TRAFO pUP089 A B antibiotics test Nad Nic 2011-08-25.jpg

conclusions:

  • elimination of ampicillin resistance has worked
  • pUP089 vector will be used for mdnA library


Sequencing of pSB1K3 constitutive and Ara as well as pSB1A3 constitutive and Ara from 2011-08-24

Time: 19:00-

Investigators: Jessica, Nadja

Materials:

  • pSBA3-YFP+const C = 470,8 ng/µl
  • pSBA3-CFP+const A = 889,2 ng/µl
  • pSBA3-CFP+const C = 692,8 ng/µl
  • pSBK3-YFP+const A = 495,0 ng/µl
  • pSBK3-CFP+const A = 1142,0 ng/µl
  • pSBK3-YFP+ara V = 380,1 ng/µl
  • Primer : VF2
  • eurofins mwg/ operon Label-Barcodes

Method:

  • 70µg/µl DNA, total volume of 15µl
  • 2 pmol/µl Primer, ca. 10µl for each sample

Further task:

  • analysing results


Transformation of pSB1C3 with several mdn genes/ promotor and pSB1T3-YFP I/II with several promotor

Investigators: Niels, Jessica

Material:

  • XL1-blue (competent)
  • RV-308 (competent)
  • ligation products :
    • pSB1C3 + mdnB
    • pSB1C3 + mdnC
    • pSB1C3 + mdnD
    • pSB1C3 + mdnE
    • pSB1C3 + mdnBC
    • pSB1C3 + mdnABC
    • pSB1C3 + mdnDE
    • pSB1C3 + Ara
    • pSB1C3 + Lac
    • pSB1C3 + const
    • pSB1C3 + H2O
    • pSB1T3-YFP II + Ara
    • pSB1T3-YFP II + Lac
    • pSB1T3-YFP II + const
    • pSB1T3-YFP II + H2O
    • pSB1T3-YFP I + Ara
    • pSB1T3-YFP I + Lac
    • pSB1T3-YFP I + const
    • pSB1T3-YFP I + H2O
  • for pSB1T3 plasmids RV-308 cells were used
  • for others: Xl1-blue
  • LB-Agar
  • tetracycline
  • chloramphenicol

Method:

  • addition of 2 µl ligation reaction to XL1-blue cells
  • incubation 60 min on ice,
  • heat shock 90 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates:
    • pSB1T3
      • 100 µg/ml tetracyclin
    • pSB1C3
      • 100 µg/ml chloramphenicol
  • incubation over night at 37°C

Further tasks:
control cell clones

Results (from 2011-08-26):

  • for transformations of pSB1C3 + mdn fragments 2 clones were picked from each plate
  • plates of pSB1C3 and pSB1T3 with promoters were thrown away because of too many colonies on control


PCR of complete mdn cluster for biobrick-construction

Time: 2011-08-25

Investigators: Nadine, Jessica

Material:

  • pARW089, 20.8.11, 3.3 ng/µl
  • pARW071, 27.5.11, 6.3 ng/µl
  • dNTPs
  • primer 77, 78, 79, 80
  • HF Phusion Buffer 5x* Phusion Polymerase

Method:

  • 2µl pARW089, 1µl pARW071, respectively
  • 1µl dNTPs
  • 2µl forward primer (10mM)
  • 2µl reverse primer (10mM)
  • 10µl HF Phusion Buffer 5x
  • 0.5 µl Phusion Polymerase
  • 31.5 µl water (total volume= 50µl)
  • reaction
Step Temperature Time
Hot Start 98°C Hold
Initial denaturation 98°C 30 sec
Denaturation 95°C 30 s
Annealing 59°C 60 s
Extension 72°C 2 min
DenaturationII 95°C 30 s
AnnealingII 59°C 60 s
ExtensionII 72°C 2 min
Final extension 68°C 5 min

Result:

  • three different PCR samples
    • PCR sample 1: mdnABCDE from pARW071, Primer: 77/78
    • PCR sample 2: mdnABCDE with T7 from pARW089, Primer: 77/79
    • PCR sample 3: mdnABCDE without T7 from pARW089, Primer: 77/80

Output:

  • mdnABCDE71
  • mdnABCDE89-T7
  • mdnABCDE89

Further Tasks:

  • agarose gel
  • PCR clean up
  • restriction enzyme digestion
  • ligation
  • transformation


gel purification of AraC, TEV, 14_3C and TEv vector and 14_3C vector

Investigator: Stefan

Material:

  • Gel purification kit (Machery & Nagel)

Methode:

protocol for gel purification.

Further tasks:

ligation of different fragmentsand transformation of competent E.coli XL1 blue cells.

ligation of AraC, TEV/14_3C with the TEV/14_3C vector

Investigator: Stefan

Material:

optional table caption
Column heading 1 TEV 1 µL TEV 2 µL TEV 3 µL TEV 4 µL 14_3C 1 µL 14_3C 2 µL control 14_3C vector µL control TEV vector µL
AraC 0.8 (35 ng) 1.8 (13.5 ng) 1.8 (8.8 ng) 2.3 (8.8 ng) 3.4 (7.5 ng) 1.4 (35 ng) 0 0
Protease 1.4 (11.9 ng) 1.3 (6.3 ng) 0.3 (61.9 ng) 0.7 (20.2 ng) 1.8 (7.1 ng) 3.6 (61.9 ng) 0 0
vector 5.8 (6.4 ng) 4.9 (6.4 ng) 6 (5.2 ng) 5.1 (5.2 ng) 2.8 (11.6 ng) 3. (22.2 ng) 5.8 (6.4 ng) 4.9 (6.4 ng)
buffer 1 1 1 1 1 1 1 1
ligase 1 1 1 1 1 1 1 1
H2O 0 0 0 0 0 0 2.8 5.2

Method:

ligation at room temperatur for 1 h

Further tasks:

transformation in competent cells

transformation of ligations

Investigator: Stefan

Material:

Method:

streak out of LB plattes with CM, use 150 µL and spin down the rest and streak it out, too.

Further tasks:

checking clones

over night culture of pUP089 A/*B from 24.08.2011

Investigators: Niels, Nadja

Materials/Method:

  • 5 ml LB media
  • 5 µl Kanamycin (50mg/ml)
    • clone of
      • pUP089 A - I
      • pUP089 A - II
      • pUP089 A - III
      • pUP089 B - I
      • pUP089 B - II
      • pUP089 B - III
  • 37°C, 250 rpm, over night

Further task:

  • miniprep


PCR of geneIII and mdnA

Investigators: Sabine

Aim:

  • amplification of mdnA and geneIII for cloning into pSB1C3

Reaction Components:

  • 2 µl/ 20 ng geneIII (cut out from pARW089)
  • 0,25 µl Taq Polymerase S (BioScience)
  • 1 µl dNTPs
  • 1 µl primer pf_geneIII_EheI_XbaI_NgoMIV
  • 1 µl primer pr_geneIII_iGEM_AatII
  • 5 µl 10x PCR Buffer S
  • 39,75 µl water


  • 5 µl/ 50 ng pak bla KDIR (mdnA)
  • 0,25 µl Taq Polymerase S (BioScience)
  • 1 µl dNTPs
  • 1 µl primer pf_mdnA_iGEM_EheI
  • 1 µl primer pr_mdnA_iGEM_AatII
  • 5 µl 10x PCR Buffer S
  • 36,75 µl water

Further tasks:

  • analytic gel electrophoresis
  • purification
  • digestion


Analytic gel electrophoresis to control PCR

Investigators: Sabine

Time: 12:00-13:00


Aim: control of PCR


Material/Method:

  • PCR products (mdnA and geneIII)
  • 1 % agarose gel
  • 1x TAE buffer
  • Gel Red
  • DNA Ladder Mix (1:10) (Fermentas)
  • 6x Loading Dye (Fermentas)
  • Gel Red

Result:

  • PCR product with right band sizes
  • mdnA ca. 200 bp
  • geneIII ca. 500 bp

Further tasks:

  • purification
  • digestion


prepare samples for sequencing (created pPDV089)

Investigators: Sabine

Time: 12:00-13:00

Aim: sequencing (GATC)

Material/Method:

  • purified plasmids of clones 3F6, 3F8, 2S7 and 2S14 (80 ng/µl, 20 µl total volume)
  • primer mdnA_6 (10 pmol/µl, 30 µl total volume)

Further tasks: control sequence


digestion of created pPDV089 for deletion of kanamycin gene

Investigators: Laura, Sabine

Aim:

  • inactivation of kanamycin resistence gene
  • reason: helper plasmid contains also kanamycin restistence gene
  • enable selection of E. coli cells containing both helper plasmid and phage display vector

Time: 14:00-14:30

Reaction components:

  • 3 µl pPDV089 (from clones 3F6, 3F8, 2S7 and 2S14)
  • 1 µl restriction enzyme NsiI (Fermentas, AG Dittmann)
  • 2 µl buffer (Fermentas, AG Dittmann)
  • 14 µl water

Reaction conditions:

  • over night at 37°C


Digestion of PCR products geneIII and mdnA for cloning into pSB1C3

Investigator: Laura, Sabine

Aim: cloning of mdnA, geneIII and mdnA/geneIII into pSB1C3

Time: 14:30-16:00

Material/Method:

  • 30 µl PCR product mdnA
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme PstI
  • 4 µl NEB 10x buffer 2
  • 0,4 µl BSA
  • 3,6 µl water
  • 1,5 h, 37°C


  • 20 µl PCR product geneIII
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme PstI
  • 3 µl NEB 10x buffer 2
  • 4,7 µl water
  • 0,3 µl BSA
  • 1,5 h, 37°C


  • 20 µl PCR product geneIII
  • 1 µl restriction enzyme NgoMIV
  • 1 µl restriction enzyme PstI
  • 3 µl NEB 10x buffer 1
  • 0,3 µl BSA
  • 4,7 µl water
  • 1,5 h, 37°C


  • 20 µl PCR product mdnA
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme AgeI
  • 3 µl NEB 10x buffer 1
  • 4,7 µl water
  • 0,3 µl BSA
  • 1,5 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • ligation of mdnA and geneIII into pSB1C3


Agarose gel electrophoresis for purification of digested PCR products

Investigator: Sabine

Aim: control and purification of digested PCR products mdnA and geneIII

Time: 16:30-17:30

Material/Method:

  • PCR products (mdnA and geneIII)
  • 1 % agarose gel
  • 1x TAE buffer
  • Gel Red
  • DNA Ladder Mix (1:10) (Fermentas)
  • 6x Loading Dye (Fermentas)
  • Gel Red


76th Labday 2011-08-26

miniprep of pUP089 clones

Investigators: Nadine

Time: 2011-08.26, 8:00-9:30

Aim:

  • glycerol stocks
  • purification of pUP089 plasmids for mdnA library (and screening)

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 50µl Elution buffer
  • Check concentration with NanoDrop
  • o.n. cultures:
    • pUP089 A I
    • pUP089 A II
    • pUP089 A III
    • pUP089 B I
    • pUP089 B II
    • pUP089 B III

Results:

    • pUP089 A I : 498.5 ng/µl
    • pUP089 A II: 465.2 ng/µl
    • pUP089 A III: 462.2 ng/µl
    • pUP089 B I: 426.1 ng/µl
    • pUP089 B II: 443.1 ng/µl
    • pUP089 B III: 448.9 ng/µl

Output:

  • # P15: pUP089 A1
  • # P16: pUP089 A II
  • # P17: pUP089 A III
  • # P18: pUP089 B I
  • # P19: pUP089 B II
  • # P20: pUP089 B III
  • glycerol stocks in XL1 blue:
    • # G2 pUP089 A I
    • # G3 pUP089 A II
    • # G4 pUP089 A III
    • # G5 pUP089 B I
    • # G6 pUP089 B II
    • # G7 pUP089 B III


PCR of complete mdn cluster for biobrick-construction

Investigators: Steffi, Nadine, Katharina

Material:

  • pARW089
  • pARW071
  • dNTPs
  • primer 77, 78, 79, 80
  • HF Phusion Buffer 5x* Phusion Polymerase

Method:

  • 2µl pARW089, 1µl pARW071, respectively
  • 1µl dNTPs
  • 2µl forward primer (10mM)
  • 2µl reverse primer (10mM)
  • 10µl HF Phusion Buffer 5x
  • 0.5 µl Phusion Polymerase
  • 31.5 µl water (total volume= 50µl)
  • reaction
Step Temperature Time
Hot Start 95°C Hold
Initial denaturation 95°C 30 sec
Denaturation 95°C 30 s
Annealing 51°C 60 s
Extension 68°C 6.5 min
DenaturationII 95°C 30 s
AnnealingII 63°C 60 s
ExtensionII 68°C 6.5 min
Final extension 68°C 50 min

Result:

  • three different PCR samples
    • PCR sample 1: pARW071 + primer 77/78 = mdnABCDE71
    • PCR sample 2: pARW089 + primer 77/79 = mdnABCDE89+T7
    • PCR sample 3: pARW089 + primer 77/80 = mdnABCDE89

Further Tasks:

  • gel electrophoresis
  • PCR clean up
  • restriction enzyme digestion
  • ligation
  • transformation


digest of PCR products from 25.08.2011

Investigators: Niels

Aim:

  • digest of PCR - products

Materials: PCR from 25.08.2011

  • PCR loop
  • PCR 1 Libary
  • PCR 2 Libary

Sample:

  • 0,5 µl DNA
  • 1 µl Aat II (Roche)
  • 3 µl 10x Buffer (Roche)
  • 25,5 µl water
  • total volume 30 µl
    • 37°C
    • 3 hours

further tasks:

  • ligation with pUP089


Repeated ligation of digested mdn fragments and pSB1C3 ( from 2011-08-24)

Investigators: Jessica, Nadja

Time: 2011-08-26, 18:00

Materials

Ligation:

Insert [µl] Vector [µl]
mdnB 6 C3 2
mdnC 6 C3 2
mdnD 7 C3 1
mdnE 5 C3 3
mdnBC 5 C3 3
mdnDE 5 C3 3
mdnABC 5 C3 3
H20 5 C3 3
  • 1 µl 10x Buffer
  • 1 µl T4 Ligase
  • over night by 14°C

Further tasks:

  • transformation


Agarose gel and Gel extraction of pUP089 and the three libraries as well as their ligation

Investigators: Jessica, Nadine, Nadja

Time: 2011-08-26, 16:00

Aim

  • Build up a Library of mutated mdnA`s

Materials

  • digests of:
  • pUP089
  • libraries 800, 2000, loop

Agarose gel

Gel 1

  • 1%: 0.5 g agarose + 50 ml 1x TAE, adding 2 µl gel red
lane Sample Volume in µl Expected size in bp
M GeneRuler™ DNA Ladder Mix (diluted 1:10) 12
1 -
2 digest pUP089 36 10029, 161

UP AG digest pUP089 2011-08-26 Jessica.jpg

Gel 2

  • 2%: 1 g agarose + 50 ml 1x TAE, adding 2 µl gel red
lane Sample Volume in µl Expected size in bp
M GeneRuler™ 100bp DNA Ladder 2
1
2 Library 1 36 161
3
4 Library 2 36 161
5 -
6 Library Loop 36 161

UP AG digest lib 2011-08-26 Jessica.jpg

Gel extraction

  • Promega- Wizard SV Gel and PCR Clean Up System
  • Eluation with 50µl Nuclease- Free Water

Nano- Drop :Concentrations

  • Library 1- digested- purified 11-26: 6,2 ng/µl
  • Library 2- digested- purified 11-26: 6,1 ng/µl
  • Library Loop- digested- purified 11-26: 7,5 ng/µl
  • pUP089: 11,3 ng/µl

Dephosphorylation of pUP089

  • add 5µl Multicore 10x Buffer (Promega)
  • add 1µl Thermosensitive Alkaline Phosphatase (Promega)
  • incubate at 37°C for 15 min
  • heat inactivation at 74°C for 15 min

Ligation

Insert [µl] Vector [µl]
Library 1 1 pUP089 7
Library 2 1 pUP089 7
Library Loop 1 pUP089 7
H2O 1 pUP089 7
  • 1 µl 10x Buffer
  • 1 µl T4 Ligase
  • over night at 14°C

Further tasks:

  • transformation


over night cultures of XL1 blue pSB1C3+mdn-combination

Time: 2011-08-26, 10:00-12:00

Investigators: Nadine, Nadja

Material:

  • plates from 2011-08-25, Niels
    • pSB1C3+mdnB clone 1
    • pSB1C3+mdnB clone 2
    • pSB1C3+mdnC clone 1
    • pSB1C3+mdnCclone 2
    • pSB1C3+mdnD clone 1
    • pSB1C3+mdnD clone 2
    • pSB1C3+mdnE clone 1
    • pSB1C3+mdnE clone 2
    • pSB1C3+mdnABC clone 1
    • pSB1C3+mdnABC clone 2
    • pSB1C3+mdnBC clone 1
    • pSB1C3+mdnBC clone 2
    • pSB1C3+mdnDE clone 1
    • pSB1C3+mdnDE clone 2
  • 25 mg/ml chloramphenicol
  • LB-medium

Protocol:

  • 5 ml LB and 5 µl chloramphenicol
  • tip w/ colony
  • incubation: 37°C, 200 rpm, over night


Glycerol stocks of E. coli containing created pPDV089

Investigator: Sabine

Time: 10:30-10:30

Material/Method:

  • 300 µl glycerol per stock
  • 700 µl cell culture per stock
  • storage at 80 °C


Gel electrophoresis to control digestion of pPDV089 with NsiI

Investigators: Sabine

Time: 10:30-12:00

Aim: control of digestion and purification

Material/Method:

  • digested pPDV089 (clones 3F6, 3F8, 2S7 and 2S14)
  • 1 % agarose gel
  • 1x TAE buffer
  • Gel Red
  • DNA Ladder Mix (1:10) (Fermentas)
  • 6x Loading Dye (Fermentas)
  • Gel Red


  • purification see protocol NucleoSpin ExtractIII kit

Result:

  • right band sizes
  • vector ca. 10 kb
  • 2 bands closed to each other near 10 kb (except 3F8), both were separately cut out of the gel)
  • deleted part of kanamycin gene ca. 300 bp

Further tasks:

  • purification
  • re-ligation


PCR of geneIII

Investigators: Sabine

Time: 12:00-14:00

Aim: amplification of geneIII for cloning into pARW089

Reaction Components:

  • 2 µl/ 20 ng geneIII (cut out from pARW089)
  • 0,25 µl Taq Polymerase S (BioScience)
  • 1 µl dNTPs
  • 1 µl primer pf_geneIII_EheI_XbaI_NgoMIV
  • 1 µl primer pr_geneIII_iGEM_AatII
  • 5 µl 10x PCR Buffer S
  • 39,75 µl DNase free water
  • prufication see protocol NucleoSpin ExtractII kit


Further tasks:

  • digestion


Ligation go geneIII and mdnA into pSB1C3

Investigator: Sabine

Aim: cloning of mdnA, geneIII and mdnA/geneIII into pSB1C3

Time: 14:00-15:30

Material/Method:

  • 1,9 µl PCR product geneIII (36 µg/µl)
  • 6,1 µl pSB1C3 (17 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 1 µl T4 Ligase (Fermentas)
  • 1 h at room temperature


  • 2,4 µl PCR product mdnA (12 µg/µl)
  • 6,6 µl pSB1C3 (17 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 1 µl T4 Ligase (Fermentas)
  • 1 h at room temperature


  • 1,9 µl PCR product mdnA (12 µg/µl)
  • 1,6 µl PCR product geneIII (36 µg/µl)
  • 4,5 µl pSB1C3 (17 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 1 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Re-ligation of NsiI-digested pPDVs089

Investigator: Sabine

Aim: create pPDV089 without kanamycin resistence

Time: 14:30-16:00

Material/Method:

  • 17 µl NsiI-digested pPDVs089 (3F6, 3F8, 2S7 and 2S14, DNA from upper and lower bands)
  • 1 µl T4 ligase buffer (Fermentas)
  • 2 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Ligation of geneIII into pARW089

Investigator: Sabine

Aim: cloning of geneIII into pARW089

Time: 15:00-17:30

Material/Method:

  • 1,5 µl PCR product geneIII (17 µg/µl)
  • 6,5 µl pARW089 (30 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 1 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Transformation of created vectors in E. coli

Investigators: Sabine

Aim:amplification of vectors

Time: 18:00-21:00

Material:

  • pPDV089 without kanamycin resistence (3F6, 3F8, 2S7 and 2S14)
  • pARW089 containing only geneIII (no mdnA)
  • pSB1C3 containing mdnA, geneIII or mdnA/geneIII
  • agar plates containing chloramphenicol (pSB1C3)
  • agar plates containing kanamycin, ampicillin and kanamycin+ampicillin (pPDV)
  • agar plates containing kanamycin (pARW089)

Method:

  • addition of 4 µl ligation reaction to XL1-blue cells
  • incubation 25 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates containing 100 µg/ml tetracyclin and 100 µg/µl ampicillin
  • storage over night at 37°C

Further tasks:
control cell clones


77th Labday 2011-08-27

Agarose gel of PCR prducts mdnABC and PCR purification

Time: 2011-08-27, 10:00-12:00

Investigators: Nadine

Aim:

  • prove PCR
  • purification of PCR prducts

Materials:

  • PCR products from 2011-08-26 , Katharina
    • mdnABCDE71
    • mdnABCDE89+T7
    • mdnABCDE89
  • Promega- Wizard SV Gel and PCR Clean Up System (elution in 50 µl elution buffer)
  • Agarose (BioRad)
  • 1x TAE
  • gel red
  • loading dye (promega)
  • 1:100 ladder mix (Fermentas)

Protocol:

  • 1%: 0.5 ge agaros + 50 ml 1xTAE buffer, 2 µl gel red
  • PCR clean up: following protocol from kit

Results:

lane Sample Volume in µl Expected size in bp
M Ladder 12
1
2 mdnABCDE from pARW071 12 (2 µl PCR product) ~6500
3
4 mdnABCDE from pARW089 w/ T7 12 (2 µl PCR product) ~6500
5 -
6 mdnABCDE from pARW089 without T7 12 (2 µl PCR product) ~6500

UP AG PCR mdn cluster pARW071 pARW089a pARW089b Nad 2011-08-27.jpg

  • no product for mdnABCDE of pARW089 w/ T7
  • PCR clean up:
    • mdnABCDE from pARW071: 36.6 ng/µl
    • mdnABCDE from pARW089 w/ T7: 37.6 ng/µl
    • mdnABCDE from pARW089 without T7: 63.9 ng/µl

Further tasks:

  • digest w/ EcoRI and SpeI (also pSB1C3)
  • repeat PCR (third time)


competent cells - E.coli XL1 blue & RF308

Investigator: Steffi

Aim: produce competent cells

Materials/Methods:

TFB I 1000ml 200ml
100mM Rubidium Chloride 12.1 2.42g
30mM Potassium Acetate 2.944 0.59g
10mM Calcium Chloride 1.47 0.29g
15% w/v Glycerol (87%) 150 34.5g

Adjust pH to 5.8 with acetic acid

Filter sterilize the solution

TFB II 500ml 100ml
50mM Rubidium Chloride 0.6 0.121g
10mM MOPS 1.05 0.210g
75mM Calcium Chloride 5.51 1.100g
15% w/v Glycerol (87%) 75 17.24g

Adjust pH to 7.0 with KOH

Filter sterilize the solution

Work always sterile and cold and speedy!

  • All volumes deal with the common cellline!
  • Prepare 68 Eppis (1,5µl)
  • get liquid nitrogen
  • prepare 5 ml LB-Medium with the specific antibiotic (for XL1-blue: Tet, for BL21: none!), inoculate and incubate over night
  • prepare 200 ml LB-Medium with the specific antibiotic, inoculate with 2 ml of the over-night-culture
  • grow while shaking at 37°C, 190 rpm to an OD600 at 0,4-0,6
  • keep cell suspension in sterile falcons (50 ml) 10 min on ice, then centrifuge for 5 min, 4°C, 4000 rpm
  • discard supernatant, carefully resuspend on ice with 40 ml icecold TFB I and keep 10 min on ice
  • centrifuge for 5 min, 4°C, 4000 rpm
  • discard supernatant, carefully resuspend pellet in 8 ml TFB II
  • aliquot in Eppis: 50µl per tube and store immediately at liquid nitrogen and afterwards at -80 °C

Results:

  • 34 tubes RV308 for expression(50 µl competent cells at -80°C)
  • 34 tubes XL1 blue for transformation(50 µl competent cells at -80°C)

Further tasks:
check by transformation


miniprep of several mdn clones and glycerole stocks

Investigators: Nadine, Katharina

Time: 2011-08-27, 11:00-12:00

Aim:

  • glycerol stocks
  • purification of pSB1C3+mdnX plasmids for mdnX biobricks (and screening)

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 50µl Elution buffer
  • Check concentration with NanoDrop
  • o.n. cultures (from 2011-08-26, Nad/Nad):
    • pSB1C3+mdnB clone 1
    • pSB1C3+mdnB clone 2
    • pSB1C3+mdnC clone 1
    • pSB1C3+mdnCclone 2
    • pSB1C3+mdnD clone 1
    • pSB1C3+mdnD clone 2
    • pSB1C3+mdnE clone 1
    • pSB1C3+mdnE clone 2
    • pSB1C3+mdnABC clone 1
    • pSB1C3+mdnABC clone 2
    • pSB1C3+mdnBC clone 1
    • pSB1C3+mdnBC clone 2
    • pSB1C3+mdnDE clone 1
    • pSB1C3+mdnDE clone 2

Results:

    • pSB1C3+mdnB clone 1: 778.3 ng/µl
    • pSB1C3+mdnB clone 2: 600.5 ng/µl
    • pSB1C3+mdnC clone 1: 1031.7 ng/µl
    • pSB1C3+mdnCclone 2: 843.3 ng/µl
    • pSB1C3+mdnD clone 1: 482.8 ng/µl
    • pSB1C3+mdnD clone 2: 541.1 ng/µl
    • pSB1C3+mdnE clone 1: 734.4 ng/µl
    • pSB1C3+mdnE clone 2: 768.2 ng/µl
    • pSB1C3+mdnABC clone 1: 853.4 ng/µl
    • pSB1C3+mdnABC clone 2: 690.3 ng/µl
    • pSB1C3+mdnBC clone 1: 626.9 ng/µl
    • pSB1C3+mdnBC clone 2: 764 ng/µl
    • pSB1C3+mdnDE clone 1: 899.4 ng/µl
    • pSB1C3+mdnDE clone 2: 525.6 ng/µl

Output:

  • plasmids: see results (stored in -20°C: green box, red label: mdn biobricks)
  • glycerol stocks in XL1 blue (stored in -80°C, glycerole box #2):
    • pSB1C3+mdnB clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnB clone 2, 27.8.11, Nad/Kat
    • pSB1C3+mdnC clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnCclone 2, 27.8.11, Nad/Kat
    • pSB1C3+mdnD clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnD clone 2, 27.8.11, Nad/Kat
    • pSB1C3+mdnE clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnE clone 2, 27.8.11, Nad/Kat
    • pSB1C3+mdnABC clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnABC clone 2, 27.8.11, Nad/Kat
    • pSB1C3+mdnBC clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnBC clone 2, 27.8.11, Nad/Kat
    • pSB1C3+mdnDE clone 1, 27.8.11, Nad/Kat
    • pSB1C3+mdnDE clone 2, 27.8.11, Nad/Kat

Further Tasks:

  • test digest (today)
  • sequencing (Monday, 2011-08-29)


Digestion of PCR products of complete mdn-cluster (mdnABCDE)

Investigators: Nadine, Katharina

Materials

  • pSB1C3
  • purified PCR products of mdn-cluster
  • NEB Buffer 4
  • EcoRI
  • SpeI
  • BSA

Method

  • digestion of inserts (PCR products of mdn-cluster)
    • 50 µl purified PCR product
    • 1.5 µl EcoRI
    • 1.5 µl SpeI
    • 6 µl NEB Buffer 4
    • 0.6 µl BSA
    • 0.4 µl sterile water
  • digestion of vector (pSB1C3 235.0 ng/µl)
    • 3 µl NEB Buffer 4
    • 4 µl pSB1C3
    • 0.3 µl BSA
    • 1.5 µl EcoRI
    • 1.5 µl SpeI
    • 19.7 µl sterile water

Agarose gel

  • 0.8%: 0.4 g agarose + 50 ml 1x TAE, adding 2 µl gel red
lane Sample Volume in µl Expected size in bp
M Ladder 12
1 mdnABC from pARW071, digested  ?? ~6500
2 mdnABC from pARW089 w/ T7, digested  ?? ~6500
3 mdnABC from pARW089 without T7, digested  ?? ~6500
4 pSB1C3, digested ~150, 2400

UP AG digest mdnCluster pSB1CR Eco Spe Kat Nad 2011-08-27.jpg

Conclusions

  • only mdnABCDE89 has worked

Further tasks:

  • repeat PCR for mdnABCDE71 and mdnABCDE89 and mdnABCDE89+T7
  • Transformation of pSB1C3+mdnABCDE89 in XL1 blue


Transformation of ligation: pUP089 + Lib-1/2, pSB1c3 + several mdn

Investigator: Niels

Material:

  • XL1-blue (competent)
  • ligation products from ligation from 2011-08-26/25

old competent cells

    • pSB1C3 + H2O
    • pSB1C3 + mdnBC
    • pSB1C3 + mdnB
    • pUP089 + puB control
    • pUP089 + Lib-loop
    • pUP089 + Lib-1
    • pUP089 + Lib-2

new competent cells

    • pSB1C3 + mdnE
    • pSB1C3 + H2O
    • pSB1C3 + mdnD
    • pSB1C3 + mdnABC
    • pSB1C3 + mdnDE
    • pSB1C3 + mdnC
    • puP089 + Lib-1
  • LB-Agar
    • chloramphenicol
    • kanamycine

Method:

  • addition of 2 µl ligation reaction to XL1-blue cells
  • incubation 60 min on ice,
  • heat shock 90 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates:
    • pUP089
      • 100 µg/ml kanamycin
    • pSB1C3
      • 100 µg/ml chloramphenicol
  • incubation for 20 hrs at 37°C

Further tasks:
control cell clones


Ligation of 3x pUP089 + Lib-2

Investigators: Niels

Material:

  • pUP089 (restricted with EheI/AatII) (Vector)
  • Lib-2 (Insert)

Method:

  • 7 µl pUP089
  • 1 µl Insert
  • 1 µl Ligase buffer
  • 1 µl T4 Ligase

Further tasks:

Transformation


Ligation of mdnABCDE89 + pSB1C3

Investigators: Katharina

Material:

  • pSB1C3 (Vector)
  • mdnABCDE89 (Insert)

Method:

  • ligation
    • 7 µl purified PCR product of mdn-cluster
    • 1 µl pSB1C3
    • 1 µl Ligase buffer
    • 1 µl T4 Ligase
  • ligation control
    • 7 µl sterile water
    • 1 µl pSB1C3
    • 1 µl Ligase buffer
    • 1 µl T4 Ligase


Mini-Prep of the positiv clones from an overnight culture

Investigator: Stefan

Material:

  • Mini-Prep Kit (machery & Nagel)

Method:

Standard protocol 5.1 for plasmid preparation. And do glycerol stock cultures of all them.

Further tasks:

Send plasmids for sequencing

test digest of pSB1C3+mdncombinations (several mdn clones/combinations)

Time: 2011-08-27,16:30-18:30

Investigators: Nadine

Aim: prove of Insert (mdn combinations)

Materials:

  • pSB1C3+mdn-combinations (miniprep from today, see above, Nad/Kat)
  • HindIII, PvuII, ClaI, AvaI, HpaI (NEB)
  • Buffer 4 and 2 (NEB, 10x)
  • BSA

Plan:

insert plasmid size in bp enzymes buffer Expected size in bp
mdnC 3385 HindIII 2 363, 3022
mdnD 2944 PvuII 4 220, 591, 2133
mdnE 4474 ClaI 4 + BSA 769, 3705
mdnABC 4852 HindIII, AvaI 2 363, 836, 3653
mdnBC 4419 HindIII, AvaI 2 363, 836, 3220
mdnDE 5154 HpaI 4 1329, 3825


Digestion protocol (one enzyme)

  • 1 µl DNA
  • 0.5 µl enzyme (see table)
  • 2 µl 10x buffer
  • 16.5 µl pure water

Digestion protocol (two enzymes)

  • 1 µl DNA
  • 0.5 µl enzyme I
  • 0.5 µl enzyme II
  • 2 µl 10x buffer
  • 16 µl pure water

Digestion protocol (two enzymes and BSA)

  • 1 µl DNA
  • 0.5 µl enzyme I
  • 0.5 µl enzyme II
  • 2 µl 10x buffer
  • 0.2 µl BSA
  • 15.8 µl pure water


  • total: 20µl
  • 37°C for over night

Conclusions:

  • annotation of mdnB in pARW089 (genious) might be wrong

Further tasks:

  • agarose gel
  • check annotation of mdnB


Troubleshooting of transformed cells

Investigator: Stefan

Aim:

  • check of vector is digested at all

Materials:

heat shock transformation

Method:

heat shock transformation

Output:

UP 2011-08-27 test-transformation-of-digest-pre-vector 002 Stefan006.jpg

UP 2011-08-27 test-transformation-of-digest-vector 001 Stefan005.jpg


78th Labday 2011-08-28

comparison of "new" and "old" competent cells

Investigators: Katharina

Results:

UP comparison of competent cells Katharina 2011-08-28.jpg

check plates from transformation (pSB1C3 w/ mdn combinations in XL1 blue, 2011-08-27)

Time: 2011-08-28, 12:00-12:30

Investigators: Katharina, Nadine

Aim:

  • build biobricks w/ mdn combinations

Material:

  • plates
  • scanner

Results:

UP TRAFO mdn Biobrick clones Steffis comp zellen 2011 08 28.jpg

conclusions:

  • Trafo has worked

Further tasks:

  • pick colonies from plates
  • mini prep tomorrow
  • test digest (see 2011-08-27)
  • sequencing


Agarose gel of PCR prducts mdnABC and PCR purification

Time: 2011-08-27, 10:00-12:00

Investigators: Nadine, Katharina

Aim:

  • prove insert of pSB1C3 with mdn-combinations (biobricks) (miniprep from 2011-08-27, Nad/Kat)

Materials:

  • Agarose (BioRad)
  • 1x TAE
  • gel red
  • loading dye (promega)
  • 1:100 ladder mix (Fermentas)
  • 1kb DNA ladder (Promega)

Protocol:

  • 2 x 1%: 0.5 g agarose + 50 ml 1xTAE buffer, 2 µl gel red

Results:

  • gel 1
lane sample enzymes volume in µl Expected size in bp
M1 1:100 DNA ladder mix, Fermentas 12
1 - - - -
2 mdnABC 1 HindIII, AvaI 24 363, 836, 3653
3 mdnABC 2 HindIII, AvaI 24 363, 836, 3653
4 - - - -
5 mdnBC 1 HindIII, AvaI 24 363, 836, 3220
6 mdnBC 2 HindIII, AvaI 24 363, 836, 3220
7 - - - -
8 mdnC 1 HindIII 24 363, 3022
9 mdnC 2 HindIII 24 363, 3022
10 - - - -
M2 1kb DNA ladder, Promega - 6 -
  • gel 2
lane sample enzymes volume in µl Expected size in bp
M1 1:100 DNA ladder mix, Fermentas 12
1 - - - -
2 mdnD 1 PvuI 24 220, 591, 2133
3 mdnD 2 PvuI 24 220, 591, 2133
4 - - - -
5 mdnDE 1 HpaI 24 1329, 3825
6 mdnDE 2 HpaI 24 1329, 3825
7 - - - -
8 mdnE 1 ClaI 24 769, 3705
9 mdnE 2 ClaI 24 769, 3705
10 - - - -
M2 1kb DNA ladder, Promega - 6 -

UP AG mdn biobricks testdigest Nad Kat 2011-08-28.jpg

Conclusions:

  • only D1 (Gel 2, lane 2) seems to be okay


over night cultures of XL1 blue pSB1C3+mdn-combination

Time: 2011-08-26, 10:00-12:00

Investigators: Katharina

Material:

  • plates from 2011-08-27, Niels

new competent cells

    • pSB1C3 + mdnE
    • pSB1C3 + mdnD
    • pSB1C3 + mdnABC
    • pSB1C3 + mdnDE
    • pSB1C3 + mdnC
  • each plate: 3 clones
  • 25 mg/ml chloramphenicol
  • LB-medium

Protocol:

  • 5 ml LB and 5 µl chloramphenicol
  • tip w/ colony
  • incubation: 37°C, 200 rpm, over night

Output:

  • 15 tubes in shaker:
    • pSB1C3 + mdnE: 1, 2, 3
    • pSB1C3 + mdnD: 1, 2, 3
    • pSB1C3 + mdnABC: 1, 2, 3
    • pSB1C3 + mdnDE: 1, 2, 3
    • pSB1C3 + mdnC: 1, 2, 3

Further tasks:

  • mini prep tomorrow


Production of TEV and 14_3C biobricks part 1

Aim: indtroduction of iGEM restriction sites to produced mutated TEV and 14_3C Fragments.

Primer TEV:

(1) f_TEV_ACCAGC, r_TEV_iGEM_Eco81l

(2) r_TEV_ACCAGC, f_TEV_iGEM

Primer 14_3C:

(1) f_14_3C_ACCAGC, r_14_3C_iGEM_Eco81l

(2) r_14_3C_ACCAGC, f_14_3C_iGEM

Methode:

PCR

  • Template: 1µl (TEV or 14_3C <10ng)
  • Nucleotides: 1µl of 10mM ready to use dNTP mix
  • 5µl 10x Amplification buffer S
  • 2µl 25mM MgCl2
  • 2,5µl primers = 25pmol absolute (2,5µl of each primer)
  • 35,5µl of pure water
  • 0,5µl TaqPol


Program:

  • Denat: 3min 94°C
  • 5x:

Denat: 30sec 94°C

Anneal:30sec 55°C

Extend:30sec 72°C

  • 25x:

Denat: 30sec 55°C

Anneal:30sec 55°C

Extend:30sec 72°C

  • Final Extend: 10min 72°C


Further Tasks:

PCR purification of PCR products and Annealing of produced fragments


Transformation of pSB1C3+mdnABCDE89 and pUP089+library2

Investigators: Katharina, Steffi

Aim: Transformation of Ligation

Time: 2011-08-28, 11:00-13:00

Materials:

  • competent E. coli cells (XL1-Blue, 2011-08-27, Steffi)
  • ligation products: pSB1C3+mdnABCDE89 (2011-08-27, Katharina), pUP089+Lib2 (2011-08-27, Niels)

Method:

  • addition of 2 µl ligation reaction to cells (XL1-blue) in 1.5 ml Eppi,
  • incubation 25 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 5 min on ice,
  • addition of 750 µl LB medium,
  • incubation at 37 °C shaking for 60 min,
  • plating on LB medium with appropriate antibiotic (Cm, Kan)
  • storage over night at 37°C

Further tasks:

  • Picking clones for overnight culture
  • Producing glycerol stocks

Output:

  • 10 plates w/ Kan: mdn-lib1
  • 2 plates w/ Cm: pSB1C3+mdnABCDE89 (and control)


overnight culture of picked E. coli clones transformed with pPDV089 to control deletion of kanamycin gene

Investigators: Sabine

Aim: control deletion of kanamycin gene in cteated pPDV089

Method/Materials:

  • 3 clones from pPDV089_3F6
  • 3 clones from pPDV089_3F8
  • 3 clones from pPDV089_2S7
  • 3 clones from pPDV089_2S14
  • each clone picked 2x: one for growing in LB medium with kanamycin, one in LB medium with ampicillin
  • 5 ml LB medium per clone
  • storage over night at 37°C and 800 rpm

Further tasks:

  • control, whether clones grew in presence of ampicillin but not of kanamycin

Results:

  • clones grew in presence of both kanamycin and ampicillin
  • kanamycin deletion didn`t work out


79th Labday 2011-08-29

check transformation from yesterday (pSB1C3+mdnABCDE89 and pUP089+mdn-Lib2)

Investigators: Nadine, Steffi

Aim: check transformation

Time: 2011-08-28, 8:20-8:40

Materials:

  • Transformations from yesterday (2011-08-28, Kat)

Conclusions:

  • transfomations didn´t work
  • repeat PCRs

Further tasks:

  • repeat PCR for mdnABCDE
  • repeat PCR for mdnA-Library


miniprep of several mdn clones

Investigators: Steffi

Time: 2011-08-29, 07:00-09:30

Aim:

  • purification of 15x pSB1C3+mdnX plasmids for mdnX biobricks (and screening) from over night cultures (Katharina, 2011-08-28)

Materials

  • NucleoSpin® Plasmid (NoLid) (Macherey-Nagel)
  • elution in 50µl Elution buffer
  • Check concentration with NanoDrop
  • o.n. cultures (from 2011-08-28, Kat):
    • pSB1C3+mdnC clone 1
    • pSB1C3+mdnC clone 2
    • pSB1C3+mdnC clone 3
    • pSB1C3+mdnD clone 1
    • pSB1C3+mdnD clone 2
    • pSB1C3+mdnD clone 3
    • pSB1C3+mdnE clone 1
    • pSB1C3+mdnE clone 2
    • pSB1C3+mdnE clone 3
    • pSB1C3+mdnABC clone 1
    • pSB1C3+mdnABC clone 2
    • pSB1C3+mdnABC clone 3
    • pSB1C3+mdnDE clone 1
    • pSB1C3+mdnDE clone 2
    • pSB1C3+mdnDE clone 3

Results:

    • pSB1C3+mdnC clone 1: 434,1 ng/µl
    • pSB1C3+mdnC clone 2: 304,4 ng/µl
    • pSB1C3+mdnC clone 3: 620,7 ng/µl
    • pSB1C3+mdnD clone 1: 282,6 ng/µl
    • pSB1C3+mdnD clone 2: 413,4 ng/µl
    • pSB1C3+mdnD clone 3: 440,0 ng/µl
    • pSB1C3+mdnE clone 1: 543,7 ng/µl
    • pSB1C3+mdnE clone 2: 573,5 ng/µl
    • pSB1C3+mdnE clone 3: 440,5 ng/µl
    • pSB1C3+mdnABC clone 1: 542,3 ng/µl
    • pSB1C3+mdnABC clone 2: 267,5 ng/µl
    • pSB1C3+mdnABC clone 3: 263,6 ng/µl
    • pSB1C3+mdnDE clone 1: 366,5 ng/µl
    • pSB1C3+mdnDE clone 2: 440,2 ng/µl
    • pSB1C3+mdnDE clone 3: 340 ng/µl

Output:

  • plasmids: see results (stored in -20°C: green box, red label: mdn biobricks)

Further Tasks:

  • test digest (today)
  • sequencing (today?)


test digest of pSB1C3+mdncombinations (several mdn clones/combinations)

Investigators: Steffi

Aim: prove of Insert (mdn combinations)

Materials:

  • pSB1C3+mdn-combinations (miniprep from today, see above, Steffi)
  • HindIII, PvuII, ClaI, AvaI, HpaI (NEB)
  • Buffer 4 and 2 (NEB, 10x)
  • BSA

Plan:

insert plasmid size in bp enzymes buffer Expected size in bp
mdnC 3385 HindIII 2 363, 3022
mdnD 2944 PvuII 4 220, 591, 2133
mdnE 4474 ClaI 4 + BSA 769, 3705
mdnABC 4852 HindIII, AvaI 2 363, 836, 3653
mdnDE 5154 HpaI 4 1329, 3825


Digestion protocol (one enzyme)

  • 1 µl DNA
  • 0.5 µl enzyme (see table)
  • 2 µl 10x buffer
  • 16.5 µl pure water

Digestion protocol (two enzymes)

  • 1 µl DNA
  • 0.5 µl enzyme I
  • 0.5 µl enzyme II
  • 2 µl 10x buffer
  • 16 µl pure water

Digestion protocol (two enzymes and BSA)

  • 1 µl DNA
  • 0.5 µl enzyme I
  • 0.5 µl enzyme II
  • 2 µl 10x buffer
  • 0.2 µl BSA
  • 15.8 µl pure water


  • total: 20µl
  • 37°C for 1,5 h

Result gel:

lane sample enzymes volume in µl Expected size in bp
M1 1:100 DNA ladder mix, Fermentas 12
1 - - - -
2 mdnC 1 HindIII 24 363, 3022
3 mdnC 2 HindIII 24 363, 3022
4 mdnC 3 HindIII 24 363, 3022
5 mdnD 1 PvuII 24 220, 591, 2133
6 mdnD 2 PvuII 24 220, 591, 2133
7 mdnD 3 PvuII 24 220, 591, 2133
8 mdnE 1 ClaI 24 769, 3705
9 mdnE 2 ClaI 24 769, 3705
10 mdnE 3 ClaI 24 769, 3705
11 mdnDE 1 HpaI 24 1329, 3825
12 - - -
13 mdnDE 2 HpaI 24 1329, 3825
14 mdnDE 3 HpaI 24 1329, 3825
15 mdnABC 1 HindIII, AvaI 24 363, 836, 3653
16 mdnABC 2 HindIII, AvaI 24 363, 836, 3653
17 mdnABC 3 HindIII, AvaI 24 363, 836, 3653

UP AG testdigest biobrick mdn combinations Steffi 2011-08-29.jpg

Further tasks:

  • sequencing of mdnC (2+3), mdnD (1+3), mdnE (2)
  • repeat PCR of mdnB (wait for new primer), mdnABC and mdnDE


competent cells - E.coli XL1 blue

Investigator: Steffi

Aim: produce competent cells

Materials/Methods:

TFB I 1000ml 200ml
100mM Rubidium Chloride 12.1 2.42g
30mM Potassium Acetate 2.944 0.59g
10mM Calcium Chloride 1.47 0.29g
15% w/v Glycerol (87%) 150 34.5g

Adjust pH to 5.8 with acetic acid

Filter sterilize the solution

TFB II 500ml 100ml
50mM Rubidium Chloride 0.6 0.121g
10mM MOPS 1.05 0.210g
75mM Calcium Chloride 5.51 1.100g
15% w/v Glycerol (87%) 75 17.24g

Adjust pH to 7.0 with KOH

Filter sterilize the solution

Work always sterile and cold and speedy!

  • All volumes deal with the common cellline!
  • Prepare 80 Eppis (1,5µl)
  • get liquid nitrogen
  • prepare 5 ml LB-Medium with the specific antibiotic (for XL1-blue: Tet), inoculate and incubate over night
  • prepare 200 ml LB-Medium with the specific antibiotic, inoculate with 2 ml of the over-night-culture
  • grow while shaking at 37°C, 190 rpm to an OD600 at 0,4-0,6
  • keep cell suspension in sterile falcons (50 ml) 10 min on ice, then centrifuge for 5 min, 4°C, 4000 rpm
  • discard supernatant, carefully resuspend on ice with 40 ml icecold TFB I and keep 10 min on ice
  • centrifuge for 5 min, 4°C, 4000 rpm
  • discard supernatant, carefully resuspend pellet in 8 ml TFB II
  • aliquot in Eppis: 50µl per tube and store immediately at liquid nitrogen and afterwards at -80 °C

Results:

  • 80 tubes XL1 blue for transformation(50 µl competent cells at -80°C)

Further tasks:
check by transformation and check the resistance on agar plates with different antibiotics


check resistance of competent cells - E.coli XL1 blue

Investigator: Katharina, Steffi

Aim: check resistance of competent XL1 blue-cells on agar plates with different antibiotics

Materials/Methods:

    • competent XL1 blue-cells from 2011-08-27 and 2011-08-29 (Steffi)
    • LB-plates with Tetracycline, Chloramphenicol, Kanamycine, Ampicillin
    • plating 50 µl on agar plates
    • incubate at 37°C over night

Further tasks:
control agar plates


Oligo-Fillin for mdnA-Library (repetition)

Time: 2011-08-29, 8:30-11:30

Investigators: Nadine

Materials

  • Primer, 25 µM :
    • # 76
    • # 74: o_foc_library_2
    • # 72: o_loop_con_switch
  • Klenow-Buffer 10X
  • Klenow Fragment
  • dNTPs
  • water
  • Agarose (BioRad)
  • 1x TAE
  • gel red
  • loading dye (promega)
  • 100bp DNA ladder (Fermentas)
  • 1kb DNA ladder (Promega)

Protocol:

  • Reaction mix
    • 1 µl fw-Oligonucleotide (#76)
    • 1 µl rev-Oligonucleotide (#74 or #72)
    • 2 µl dNTPs (10 mM)
    • 2 µl Klenow-Fragment
    • 14 µl water
    • total volume: 20 µl

2. PCR program

  • name: Fillin
  • 3 min 94 °C
  • 0.3°C per s (94°C-37°C)
  • addition of 0.5 µl Klenow Fragment
  • press enter
  • 1hr 37°C

Agarose gel:

1.5 %: 0.75 g in 50 ml TAE


Results:

  • Output:
      • mdnA-Lib2, Nad, 29.8.11 (~170bp)
      • mdnA-loop, Nad, 29.8.11 (~170bp)

UP PCR mdnA library mdnA-lib2 mdnloop Nad 2011-08-29.jpg

Further tasks:

  • PCR purification


sequencing of TEV and 14_3C clones

Aim: get sequences

Methode:

send samples to GATC

Further Tasks:


Restriction of pUP089 (vector) and Lib-2/loop(Insert/PCR)

Investigator: Niels

Aim: generate vector and insert for ligation and transformation to generate a Libary

Materials/Methods:

  • pub089 (A)
    • 5 µl DNA
    • 0,5 µl Ehe I
    • 0,5 µl Aat II
    • 3 µl 10x Buffer
    • 21 µl water
      • total volume: 30µl
  • pub089 (B)
    • 1 µl DNA
    • 0,5 µl Ehe I
    • 0,5 µl Aat II
    • 3 µl 10x Buffer
    • 25 µl water
      • total volume: 30µl
  • Lib-2 (A)
    • 20 µl DNA
    • 0,5 µl Aat II
    • 3 µl 10x Buffer
    • 6,5 µl water
      • total volume: 30µl
  • Lib-2 (B)
    • 1 µl DNA
    • 0,5 µl Aat II
    • 3 µl 10x Buffer
    • 25,5 µl water
      • total volume: 30µl
  • Loop
    • 1 µl DNA
    • 0,5 µl Aat II
    • 3 µl 10x Buffer
    • 25,5 µl water
      • total volume: 30µl

over night

Further tasks:

  • purification
  • dephosphorylation
  • ligation
  • transformation


PCR of complete mdn cluster for biobrick-construction

Investigators: Niels, Nadine


Material:

  • pARW089
  • pARW071
  • dNTPs
  • primer 77, 78, 79, 80
  • HF Phusion Buffer 5x* Phusion Polymerase

Method:

  • 2µl pARW089, 1µl pARW071, respectively
  • 1µl dNTPs
  • 2µl forward primer (10mM)
  • 2µl reverse primer (10mM)
  • 10µl HF Phusion Buffer 5x
  • 0.5 µl Phusion Polymerase
  • ad 50 µl water
  • reaction
Step Temperature Time
Hot Start 98°C Hold
Initial denaturation 98°C 30 sec
Denaturation 95°C 30 s
Annealing 59°C 60 s
Extension 72°C 3,5 min
DenaturationII 95°C 30 s
AnnealingII 59°C 60 s
ExtensionII 72°C 3.5 min
Final extension 68°C 5 min

Result:

  • three different PCR samples
    • PCR sample 1: pARW071 + primer 77/78 = mdnABCDE71
    • PCR sample 2: pARW089 + primer 77/79 = mdnABCDE89+T7
    • PCR sample 3: pARW089 + primer 77/80 = mdnABCDE89

Further Tasks:

  • gel electrophoresis
  • PCR clean up
  • restriction enzyme digestion
  • ligation
  • transformation


Alignment of sequenced pPDV089 and model of pPDV089

Investigator: Sabine

Aim: control of generated phage display vector pPDV089

Materials/Methods:

  • file sent from GATC
  • software Genious

Results:

  • 4 positive clones, pPDV089 containing mdnA and geneIII (3F6, 3F8, 2S7, 2S14)

Further task:

  • deletion of kanamycin gene


PCR of geneIII and mdnA

Investigators: Sabine

Aim:

  • amplification of mdnA and geneIII for cloning into pSB1C3
  • amplification of geneIII for cloning into pARW089

Reaction Components:

  • 2 µl/ 20 ng geneIII (cut out from pARW089
  • 0,25 µl Taq Polymerase S (BioScience)
  • 1 µl dNTPs
  • 1 µl primer pf_geneIII_EheI_XbaI_NgoMIV
  • 1 µl primer pr_geneIII_iGEM_AatII
  • 5 µl 10x PCR Buffer S
  • 39,75 µl water


  • 5 µl/ 50 ng pak bla KDIR (mdnA)
  • 0,25 µl Taq Polymerase S (BioScience)
  • 1 µl dNTPs
  • 1 µl primer pf_mdnA_iGEM_EheI
  • 1 µl primer pr_mdnA_iGEM_AatII
  • 5 µl 10x PCR Buffer S
  • 36,75 µl water

Further tasks:

  • analytic gel electrophoresis
  • purification
  • digestion


80th Labday 2011-08-30

Agarose gel of PCR of complete mdn cluster for biobrick-construction

Time: 2011-08-27, 08:00-09:00

Investigators: Nadine, Steffi

Aim:

  • prove insert of pARW071/ pARW089 with complete mdn-cluster (PCR-product from 2011-08-29, Nadine)

Materials:

  • Agarose (BioRad)
  • 1x TAE
  • gel red
  • loading dye (promega)
  • 1kb DNA ladder (Promega)

Protocol:

  • 1 x 1%: 0.5 g agarose + 50 ml 1xTAE buffer, 2 µl gel red

Results:

  • gel
lane sample volume in µl Expected size in bp
M1 1kb DNA ladder (Promega) 10 -
1 mdnABCDE71 2
2 mdnABCDE89 2
3 mdnABCDE89+T7 2

UP AG pcr mdnABCDE Niels vom 29.08.11 2011-08-30-.JPG

Conclusions:

  • PCR didn`t work

Further Tasks:

  • repeat PCR
  • gel electrophoresis
  • PCR clean up
  • restriction enzyme digestion
  • ligation
  • transformation


Repeat PCR of complete mdn cluster for biobrick-construction

Investigators: Nadine, Vanessa, Steffi

Aim: repeat PCR of complete mdn cluster for biobrick-construction from 2011-08-29


Material:

  • pARW089
  • pARW071
  • dNTPs
  • primer 77, 78, 79, 80
  • Bio-X-ACT Long DNA Polymerase (Bioline)

Method:

  • 1µl pARW089 (~ 3.3ng) , 1µl pARW071 (~ 5ng)
  • 0.5µl dNTPs (100 mM)
  • MgCl2 (50 mM)
  • 1.5µl forward primer (100µM)
  • 1.5µl reverse primer (100µM)
  • 5µl OptiBuffer 10x
  • 1µl Bio-X-ACT Long DNA Polymerase (Bioline)
  • add 50 µl water
  • reaction
Step Temperature Time
Hot Start 98°C Hold
Initial denaturation 98°C 30 sec
Denaturation 95°C 30 s
Annealing 47°C 60 s
Extension 72°C 6,5 min
DenaturationII 95°C 30 s
AnnealingII 68°C 60 s
ExtensionII 72°C 6.5 min
Final extension 68°C 5 min
  • first steps: 15x
  • second step: 25x
  • program: igbBio2

Result:

  • three different PCR samples
    • PCR sample 1: pARW071 + primer 77/78 = mdnABCDE71
    • PCR sample 2: pARW089 + primer 77/79 = mdnABCDE89+T7
    • PCR sample 3: pARW089 + primer 77/80 = mdnABCDE89

Further Tasks:

  • gel electrophoresis
  • PCR clean up
  • restriction enzyme digestion
  • ligation
  • transformation


Gel extraction and purification of pUP089 (vector) and Lib-2/loop(Insert/PCR)

Investigators: Steffi

Materials:

  • Restriction products of pUP089 (vector, 10196 bp) and Lib-2/loop(Insert/PCR) from Niels (2011-08-29)
  • Agarose (BioRad)
  • 1x TAE
  • gel red
  • loading dye (promega)
  • 1kb DNA ladder (Promega)
  • 100bp DNA ladder (Fermentas)

Protocol:

  • 1 x 1%: 0.5 g agarose + 50 ml 1xTAE buffer, 2 µl gel red
  • 1 x 1.5 %: 0.75 g in 50 ml 1xTAE, 2 µl gel red

Results:

  • gel 1 (1.5%)
lane sample volume in µl Expected size in bp
M1 1kb DNA ladder (Fermentas) 10 -
M2 100bp DNA ladder (Fermentas) 10 -
1 Lib-2 (A) 30 161
2 Lib-2 (B) 30 161
3 Loop 30 161

UP AG Restriction products of Lib-2 loop Insert PCR 2011-08-30.jpg

  • gel 2 (1%)
lane sample volume in µl Expected size in bp
M1 1kb DNA ladder (Fermentas) 10 -
1 pUP089 (A) 30 10035
2 pUP089 (B) 30 10035

UP AG Restriction products of pUP089 (vector) 2011-08-30.jpg

Conclusions:

  • cut out bands from Lib-2 (B), Loop, pub089 (A) and pub089 (B)

Gel extraction

  • Macherey Nagel - NucleoSpin Extract II, protocol for DNA extraction from agarose gels
  • Elution with 50µl NE-Buffer

NanoDrop: Concentrations

  • Lib-2 (B) - digested - purified: 5,8 ng/µl
  • Loop - digested - purified: 3,9 ng/µl
  • pUP089 (A): 12,9 ng/µl
  • pUP089 (B): 23,4 ng/µl

Further tasks:

  • dephosphorylation of pub089 (B)
  • ligation
  • transformation


Dephosphorylation and Ligation of pUP089 (vector) and Lib-2/loop(Insert/PCR)

Investigators: Nadine, Steffi

Dephosphorylation of pUP089 (B)

  • add 5µl Multicore 10x Buffer (Promega)
  • add 1µl Thermosensitive Alkaline Phosphatase (Promega)
  • incubate at 37°C for 15 min
  • heat inactivation at 74°C for 15 min

Ligation

  • purified and dephosphorylated pUP089 (B) from 2011-08-30 (vector)
  • purified Lib-2 (B) (insert)
  • purified Loop (insert)
Insert [µl] Vector [µl]
Lib-2 (B) 1.8 pUP089 10
Loop 2.7 pUP089 10
  • 3 µl 10x Buffer
  • 1 µl T4 Ligase
  • add 30 µl H2O
  • 1h, RT

Further tasks:

  • transformation


Transformation of pUP089+library2

Investigators: Niels

Aim: Transformation of Ligation

Materials:

  • competent E. coli cells (XL1-Blue, 2011-08-27, 1xSteffi, 2xSabine)
  • ligation products: pUP089+Lib2 (2011-08-30, Steffi)

Method:

  • addition of 2 µl ligation reaction to cells (XL1-blue) in 1.5 ml Eppi,
  • incubation 25 min on ice,
  • heat shock 90 sec at 42°C,
  • incubation 5 min on ice,
  • addition of 750 µl LB medium,
  • incubation at 37 °C shaking for 60 min,
  • plating on LB medium with appropriate antibiotic (Kan)
  • storage over night at 37°C

Further tasks:

  • Picking clones for overnight culture
  • Producing glycerol stocks


Output:

  • 3 plates w/ Kan: mdn-lib2


sequencing of mdnC, mdnD and mdnE BioBrick

Time: 2011-08-30,14:00-14:30

Investigators: Nadine

Materials

Sequencing by GATC

  • C2 (mdnC Klon 2, Steffi, 2011-8-29)
  • C3 (mdnC Klon 3, Steffi, 2011-8-29)
  • D1 (mdnD Klon 1, Steffi, 2011-8-29)
  • D3 (mdnD Klon 3, Steffi, 2011-8-29)
  • E2 (mdnE Klon 2, Steffi, 2011-8-29)


check plates - resistance of competent E.coli XL1 blue cells

Investigators: Nadine, Steffi

Aim: check resistance of competent cells - E.coli XL1 blue (from 2011-08-27 and 2011-08-29, Steffi)

Materials:

  • agar plates from competent cells - E.coli XL1 blue from 2011-08-29 (Kat/ Ste)

Results:

  • all competent cells - E.coli XL1 blue grow on agar plates with Tetracycline
  • no E.coli XL1 clones on agar plates with Ampicillin, Kanamycine, Chloramphenicol

UP XL1 blue comp zellen.jpg

Conclusions:

  • competent cells - E.coli XL1 blue work and can be used for transformation


Assembly PCR for TEV and 14_3C

Aim: get the side-directed mutated TEV and 14_3C fragment

Methode:

Primer TEV:

(1) f_TEV_iGEM

(2) r_TEV_iGEM_BamHI

Primer 14_3C:

(1) f_14_3C_iGEM

(2) r_14_3C_iGEM_BamHI

Methode:

PCR

  • Template: 1 µL (TEV or 14_3C <10ng)
  • Nucleotides: 1 µL of 10 mM ready to use dNTP mix
  • 5 µL 10 x Amplification buffer S
  • 2 µL 25 mM MgCl2
  • 2,5 µL primers = 25 pmol absolute (2,5 µL of each primer)
  • 35,5 µL of pure water
  • 0,5 µL TaqPol

Program:

  • Denat: 4 min 94°C
  • 5x:

Denat: 1 min 94°C

Anneal: 1 min 52°C

Extend: 1 min 72°C

  • 25x:

Denat: 1 min 94°C

Anneal: 1 min 69°C

Extend: 1 min 72°C

  • Final Extend: 10min 72°C

Further Tasks:

PCR purification to check the correct sizes of fragments

Digestion of created pPDV089 for deletion of kanamycin gene

Investigators: Sabine

Aim:

  • inactivation of kanamycin resistence gene
  • reason: helper plasmid contains also kanamycin restistence gene
  • enable selection of E. coli cells containing both helper plasmid and phage display vector

Reaction components:

  • 4 µl/2µg pPDV089 (from clones 3F6, 3F8, 2S7 and 2S14)
  • 1 µl restriction enzyme NsiI
  • 2 µl buffer 3
  • 13 µl water

Reaction conditions:

  • 3 h at 37°C


Digestion of PCR products geneIII and mdnA for cloning into pSB1C3

Investigator: Sabine

Aim: cloning of mdnA, geneIII and mdnA/geneIII into pSB1C3

Material/Method:

  • 15 µl PCR product mdnA
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme PstI
  • 2 µl NEB 10x buffer 2
  • 0,2 µl BSA
  • 0,8 µl water
  • 1,5 h, 37°C


  • 15 µl PCR product geneIII
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme PstI
  • 2 µl NEB 10x buffer 2
  • 0,8 µl water
  • 0,2 µl BSA
  • 1,5 h, 37°C


  • 15 µl PCR product geneIII
  • 1 µl restriction enzyme NgoMIV
  • 1 µl restriction enzyme PstI
  • 3 µl NEB 10x buffer 1
  • 1,5 h, 37°C


  • 15 µl PCR product mdnA
  • 1 µl restriction enzyme XbaI
  • 1 µl restriction enzyme AgeI
  • 3 µl NEB 10x buffer 1
  • 0,2 µl BSA
  • 1,5 h, 37°C

Further Tasks:

  • gel electrophoresis for purification
  • ligation of mdnA and geneIII into pSB1C3


Digestion of PCR product geneIII and vector pARW089

Investigator: Sabine

Aim: pARW089 containing geneIII but not mdnA

Material/Method:

  • 15 µl PCR product geneIII
  • 1 µl restriction enzyme SfoI
  • 1 µl restriction enzyme AatII
  • 2 µl NEB 10x buffer 4
  • 1 µl water
  • 1,5 h, 37°C


  • 6 µl/2µg pARW089
  • 1 µl restriction enzyme SfoI
  • 1 µl restriction enzyme AatII
  • 1 µl NEB 10x buffer 4
  • 1 µl water
  • 3 h, 37°C

Further Task:

  • purification
  • ligation


Ligation of geneIII into pARW089

Investigator: Sabine

Aim: cloning of geneIII into pARW089

Material/Method:

  • 1,5 µl PCR product geneIII (14,5 µg/µl)
  • 15,5 µl pARW089 (11 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 2 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Re-ligation of NsiI-digested pPDVs089

Investigator: Sabine

Aim: create pPDV089 without kanamycin resistence

Material/Method:

  • 17 µl NsiI-digested pPDVs089 (3F6, 3F8, 2S7 and 2S14, DNA from upper and lower bands)
  • 1 µl T4 ligase buffer (Fermentas)
  • 2 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Ligation of geneIII and mdnA into pSB1C3

Investigator: Sabine

Aim: pSB1C3 containing mdnA, geneIII and mdnA/geneIII

Material/Method:

  • 12,5 µl PCR product geneIII (10 µg/µl)
  • 4,5 µl pSB1C3 (41 ng/µl)
  • 2 µl T4 ligase buffer (Fermentas)
  • 1 µl T4 Ligase (Fermentas)
  • 1 h at room temperature


  • 10,8 µl PCR product mdnA (7 µg/µl)
  • 6,2 µl pSB1C3 (41 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 2 µl T4 Ligase (Fermentas)
  • 1 h at room temperature


  • 4,5 µl PCR product mdnA (7 µg/µl)
  • 10 µl PCR product geneIII (7 µg/µl)
  • 2,5 µl pSB1C3 (41 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 2 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Transformation of created vectors in E. coli

Investigator: Sabine

Aim:amplification of vectors

Material:

  • pPDV089 without kanamycin resistence (3F6, 3F8, 2S7 and 2S14)
  • pARW089 containing only geneIII (no mdnA)
  • pSB1C3 containing mdnA, geneIII or mdnA/geneIII
  • agar plates containing chloramphenicol (pSB1C3)
  • agar plates containing kanamycin, ampicillin(pPDV)
  • agar plates containing kanamycin (pARW089)

Method:

  • addition of 4 µl ligation reaction to XL1-blue cells
  • incubation 25 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates containing 100 µg/ml tetracyclin and 100 µg/µl ampicillin
  • storage over night at 37°C

Further tasks:
control cell clones


gel electrophoresis of TEV and 14_3C

Aim: check sizes

Method:

80 V

UP AG 2011-08-30 assemblyPCR-4xTEV 2xPre Stefan 002.jpg

Further Tasks:

PCR purification


81th Labday 2011-08-31

Ligation of geneIII into pARW089

Investigator: Sandrina, Laura

Aim: cloning of geneIII into pARW089

Material/Method:

  • 2 µl PCR product geneIII (14,5 ng/µl)
  • 15 µl pARW089 (16 ng/µl)
  • 1 µl T4 ligase buffer (Fermentas)
  • 2 µl T4 Ligase (Fermentas)
  • 1 h at room temperature

Further task: transformation


Transformation of pARW089 containing only geneIII (no mdnA) in E.coli

Investigator: Sandrina, Laura

Aim:amplification of vectors

Method:

  • addition of 4 µl ligation reaction to XL1-blue cells
  • incubation 20 min on ice,
  • heat shock 45 sec at 42°C,
  • incubation 2 min on ice,
  • addition of 750 µl LB medium,
  • incubation 60 min at 37 °C and 750 rpm
  • plating on agar plates containing 100 µg/ml kanamycin
  • storage over night at 37°C

Further tasks:
control cell clones


overnight culture of picked E. coli clones transformed with pPDV089 to control deletion of kanamycin gene, pARW089 containing only geneIII (no mdnA), pSB1C3 containing mdnA, geneIII or mdnA/geneIII

Investigators: Sandrina, Laura

Aim: control deletion of kanamycin gene in created pPDV089, control ligation of geneIII into PARW089, control ligation of mdnA, geneIII and mdnA/geneIII into pSB1C3

Method/Materials:

  • 5 clones from pPDV089_2S14 (ampicillin)
  • 5 clones from pARW089 with geneIII (kanamycin)
  • 5 clones from pSB1C3 with mdnA (chloramphenicol)
  • 5 clones from pSB1C3 with geneIII (chloramphenicol)
  • 5 clones from pSB1C3 with mdnA/geneIII (chloramphenicol)
  • 5 ml LB medium per clone
  • storage over night at 37°C and 800 rpm

Further tasks:

  • test digestion

over night cultures of pSB1C3+mdnABC/mdnDE

time: 2011-8-31, 18:00

Investigators: Nadine

Aim: check colonies for correct plasmid

Materials:

  • agar plates from 2011-8-25, Niels (fridge):
    • pSB1C3+mdnABC
    • pSB1C3+mdnDE
  • LB medium
  • chloramphenicol (25 mg/ml)

Protocol:

  • 10 x: 10 ml LB medium + 10 µl chloramphenicol
  • pick colony from plate (from each plate 5 colonies, respectively)
  • transfer to LB medium
  • incubate over night in 37°C shaker (200 rpm)

Output:

  • over night cultures:
    • pSB1C3+mdnABC
      • clone 3
      • clone 4
      • clone 5
      • clone 6
      • clone 7
    • pSB1C3+mdnDE
      • clone 1
      • clone 2
      • clone 3
      • clone 4
      • clone 5

Further tasks:

  • miniprep
  • test digest (for protocol see 2011-8-29)


Assembly PCR for 14_3C, PCR of AraC and TEV

Aim: get the side-directed mutated TEV and 14_3C fragment

Method:

Primer TEV:

(1) f_TEV_iGEM

(2) r_TEV_iGEM_BamHI

Primer 14_3C:

(1) f_14_3C_iGEM

(2) r_14_3C_iGEM_BamHI

Methode:

PCR

  • Template: 1 µL (TEV or 14_3C <10ng)
  • Nucleotides: 1 µL of 10 mM ready to use dNTP mix
  • 5 µL 10 x Amplification buffer S
  • 2 µL 25 mM MgCl2
  • 2,5 µL primers = 25 pmol absolute (2,5 µL of each primer)
  • 35,5 µL of pure water
  • 0,5 µL TaqPol

Program:

  • Denat: 4 min 94°C
  • 5x:

Denat: 1 min 94°C

Anneal: 1 min 52°C

Extend: 1 min 72°C

  • 25x:

Denat: 1 min 94°C

Anneal: 1 min 69°C

Extend: 1 min 72°C

  • Final Extend: 10min 72°C

Further Tasks:

PCR purification to check the correct sizes of fragments