Team:Caltech/Week 11

From 2011.igem.org

(Difference between revisions)
 
(3 intermediate revisions not shown)
Line 5: Line 5:
Send BPA and degraded products to HPLC for analysis<br/>
Send BPA and degraded products to HPLC for analysis<br/>
Send 16s for sequencing using FWD and REV. <br/>
Send 16s for sequencing using FWD and REV. <br/>
 +
PCR'd R0040, K123001, B0014 and pSB3K3 for Gibson assembly of pNT002<br/>
===Results===
===Results===
Plated 16s and WT-F87A cultures show many colonies<br/>
Plated 16s and WT-F87A cultures show many colonies<br/>
Line 15: Line 16:
* 16 LB-chlor plates  
* 16 LB-chlor plates  
* 13 LB plates  
* 13 LB plates  
 +
PCR'd R0040 and pSB3K3 for Gibson assembly of pNT002<br/>
 +
PCR'd the DDT gene with new primers to add stop codons and biobrick ends.<br/>
 +
PCR'd the DDT gene with BamHI and XbaI sites and a C-terminus his tag for insertion into pET11-a. This will allow us to overexpress the protein for purification and characterization.<br/>
 +
PCR'd WT-F87A with biobrick ends.<br/>
 +
Dpn 1 digested the DDT and p450 PCRs overnight<br/>
==August 24==
==August 24==
 +
Visited the San Jose Creek Water Reclamation Plant<br/>
 +
Made more Gibson mix according to Joe's protocol.<br/>
 +
Did double restriction digest of DDT gene and p450 PCRs with biobrick ends and pSB1C3 using EcoRI and PstI.<br/>
 +
Did double restriction digest of DDT gene PCR with pET11-a insertion endings and pET11-a using BamHI and XbaI<br/>
 +
Did CIP digest of pET11a and pSB1C3<br/>
 +
Ligated DDT gene with biobrick ends into pSB1C3<br/>
 +
Ligated p450 with biobrick ends into pSB1C3<br/>
 +
Ligated DDT gene into pET11-a<br/>
 +
Transformed all ligations into 50 ul aliquots of DH5a electrocompetent cells<br/>
 +
Transformed 1 ul of 10 pg/ul pUC19 into 1 aliquot of DH5a electrocompetent cells<br/>
 +
Started overnight of pSB1C3 so there is more DNA available to use as backbones for biobrick parts to send to the registry.<br/>
 +
X-gal plating shows blue colonies; overnights of J23119-MG1655 and R0010-MG1655 to make glycerol stocks<br/>
==August 25==
==August 25==
 +
pSB1C3 concentration 118.0 ng/ul<br/>
 +
Calculated transformation efficiency of DH5a electrocompetent cells is about 2x10^8 cfu/ug<br/>
===Results===
===Results===
<table border="1">
<table border="1">
Line 55: Line 75:
<td>0</td>
<td>0</td>
</tr>
</tr>
-
<tr>
 
<tr>
<tr>
<td>pNT002 + in commercial XL-10 gold</td>
<td>pNT002 + in commercial XL-10 gold</td>
Line 64: Line 83:
<td>28</td>
<td>28</td>
</tr>
</tr>
-
<tr>
 
</table>
</table>
 +
<gallery>
 +
File: 8-25 ddt cpcr.jpg|CPCR of DDT gene lane 1 NEB 2-log ladder, 3-8 with in biocrick form, 9-14 in pET11a
 +
File: 8-25 p450 cpcr.jpg|CPCR of WT-F78A in biobrick form, lane 1 NEB 2-log ladder, 3-8 WT-F87A
 +
File: 8-25 pnt002 cpcr.jpg|CPCR of pNT002 constructed by Gibson, lane 1 NEB-2 log ladder, 3-14 pNT002
 +
</gallery>
 +
==August 26==
 +
Sent improved DDT biobrick and DDT in pET11a off fro sequencing<br/>
 +
Added X-gal to J23119 overnights to test for expression
 +
===Results===
 +
J23119-MG1655 culture turned X-gal blue; use spectrophotometer for better measurement
 +
Started culture of J23119-MG1655 in flask with glass beads for biofilm/X-gal experiment
 +
==August 27==
 +
Moved from Braun 16 to Keck 040<br/>
}}
}}

Latest revision as of 18:53, 1 September 2011


Caltech iGEM 2011



Home

Project

Data

Parts

Team

Notebook

Biosafety

Human Impact

References

Support

August 22

Send BPA and degraded products to HPLC for analysis
Send 16s for sequencing using FWD and REV.
PCR'd R0040, K123001, B0014 and pSB3K3 for Gibson assembly of pNT002

Results

Plated 16s and WT-F87A cultures show many colonies
Mix 10% glycerol solution and place in 4&degC fridge for tomorrow's electrocompetence method
Overnight shake culture of MG-1655 experimental E. coli strain

August 23

Make experimental MG-1655 strain electrocompetent
Made 53 plates today!

  • 24 LB-amp plates
  • 16 LB-chlor plates
  • 13 LB plates

PCR'd R0040 and pSB3K3 for Gibson assembly of pNT002
PCR'd the DDT gene with new primers to add stop codons and biobrick ends.
PCR'd the DDT gene with BamHI and XbaI sites and a C-terminus his tag for insertion into pET11-a. This will allow us to overexpress the protein for purification and characterization.
PCR'd WT-F87A with biobrick ends.
Dpn 1 digested the DDT and p450 PCRs overnight

August 24

Visited the San Jose Creek Water Reclamation Plant
Made more Gibson mix according to Joe's protocol.
Did double restriction digest of DDT gene and p450 PCRs with biobrick ends and pSB1C3 using EcoRI and PstI.
Did double restriction digest of DDT gene PCR with pET11-a insertion endings and pET11-a using BamHI and XbaI
Did CIP digest of pET11a and pSB1C3
Ligated DDT gene with biobrick ends into pSB1C3
Ligated p450 with biobrick ends into pSB1C3
Ligated DDT gene into pET11-a
Transformed all ligations into 50 ul aliquots of DH5a electrocompetent cells
Transformed 1 ul of 10 pg/ul pUC19 into 1 aliquot of DH5a electrocompetent cells
Started overnight of pSB1C3 so there is more DNA available to use as backbones for biobrick parts to send to the registry.
X-gal plating shows blue colonies; overnights of J23119-MG1655 and R0010-MG1655 to make glycerol stocks

August 25

pSB1C3 concentration 118.0 ng/ul
Calculated transformation efficiency of DH5a electrocompetent cells is about 2x10^8 cfu/ug

Results

Name Number of colonies
p450 biobricked in pSB1C3 ~3400
DDT gene biobrick now with stop codons in pSB1C3 ~6400
pSB1C3 ligation negative control 0
DDT gene inserted into pET11-a ~6400
pET11-a ligation negative control 27
pUC 19 in DH5a electrocompetent cells 976
DDT gene PIPE 0
VPIPE negative control 0
pNT002 + in commercial XL-10 gold 54
pNT002 - in commercial XL-10 gold 28

CPCR of DDT gene lane 1 NEB 2-log ladder, 3-8 with in biocrick form, 9-14 in pET11a

CPCR of WT-F78A in biobrick form, lane 1 NEB 2-log ladder, 3-8 WT-F87A

CPCR of pNT002 constructed by Gibson, lane 1 NEB-2 log ladder, 3-14 pNT002

August 26

Sent improved DDT biobrick and DDT in pET11a off fro sequencing
Added X-gal to J23119 overnights to test for expression

Results

J23119-MG1655 culture turned X-gal blue; use spectrophotometer for better measurement Started culture of J23119-MG1655 in flask with glass beads for biofilm/X-gal experiment

August 27

Moved from Braun 16 to Keck 040


Retrieved from "http://2011.igem.org/Team:Caltech/Week_11"