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Lab Journal

Thursday 23/6

Lab equipment was prepared: Pipette tips, 1.5 ml tubes, toothpicks, SOC, LA with 100 µg/ml ampicillin/ 100 µg/ml spectinomycin (from 1988). Recipies are given in recipies section.

Friday 24/6

Biobricks were taken out from kit by resuspending them in sterile water followed by transformation to E.coli DH5 alpha. The biobricks that were taken out are given below:

Saturday 25/6

Plates with transformants were moved to fridge.

Sunday 26/6

Transformants were inoculated in 3 ml LB + proper antibiotics to prepare for isolation of plasmid.

Monday 27/6

Plasmids that contained P1, lambda pR, RFP and Lux biobricks were isolated by using miniprep kit from Promega.

Consentrations of the biobricks were measured and were as follows:

Transformants from Lux/RFP constructs were not red as expected. It was suggested that the phenotype could be explained by presence of TetR in the system. Since tetracycline (Tc) is an inhibitor of TetR we tried to grow the transformants in sublethal consentrations of Tc. E. coli with RFP were grown in 3 ml LB with 0, 0.1, 0.3, 0.6, 1.0, 1.5 and 100 µg/ml Tc.

Tuesday 28/6

It's Jon's birthday! Happy day!

Growing the bacteria in Tc did not result in red color of the culture

lambda pR was ligated to RFP backbone:

• RFP and Luc construct were cut with EcoRI and XbaI.
• lambda pR was cut with EcoRI og SpeI

Restriction digestion was done using [http://partsregistry.org/Help:Protocols/Restriction_Digest iGEM's protocol]

Since the restriction digestion gave unexpected fragments and we had not yet seen any pigmentation, we started looking for other designs that could give the result that we wanted. We came up with a different design that used pLac promoter and lacI repressor instead of the pTet/TetR system.

To start constructing the alternative system 3 new biobricks were transformed to E. coli:

Wednesday 29/6

Lambda Pr, RFP and Lux was cut:

• RFP with XbaI and PstI
• Lux with XbaI and PstI
• Lambda Pr with SpeI and PstI

The cutting gives RFP and Lux as insert and Lambda pR the backbone.

The restriction fragments were separated on agarose gel:

The restriction fragments for lambda pR were as expected but not for RFP or Lux.

Lambda pR was isolated from gel (2110 nt) by using DNA gel extraction kit.

DNA concentration of lambda pR was measured to 5.2 ng/µl

Biobricks that were transformed yesterday were inoculated in 3 ml LB with proper antibiotics to prepare for isolation of plasmids.

Anders ordered a biobrick that should contain LacI + RBS + double terminator from iGEM HQ: BBa_K292006

Thursday 30/6

Plasmid was isolated from lac-design biobricks. Concentration of DNA:

pLac biobrick was cut with SpeI and PstI mCherry was cut with XbaI and PstI

Makes pLac backbone and mCherry insert

Tried direct ligation of restriction fragments using following reaction mix:

Reaction mix were mixed and incubated 30 min at 16C. Heat destruction of enzymes for 20 min at 80C. 2 µl of ligation mix were used for transformation. Red colonies were to be selected from transformation. Mix, spin down, 30 min 16C, heat kill 20 min 80C. Transform 2µL. Select for red colonies.

Gel picture of the separated mCherry insert (895 bp) and pLac backbone (2116 bp) fragments.

The rest of the ligation mix were separated on agarose gel and mCherry insert (895 bp) and pLac backbone (2116 bp) were isolated from gel using Quiaquick Gel Extraction Kit. DNA concentration was measured:

The directly ligated restriction fragments transformed to E. coli were plated out on LA + Amp and LA + IPTG and grown ON.

The biobrick that has been ordered (BBa_K292006) was investigated and was found to be identical to the biobrick that we were planning to make, given that the sequence is as given in the registry.

relA

The nucleotide sequence of relA (codes for protein that synthesize ppGpp) was found in database. One hickup in making this gene a biobrick; there is a PstI site inside the gene (at 1383-1388 nt if added prefix). To overcome this problem we could use partial digestion or we could introduce a silent mutation that removes the restriction site. By changing CTGCAG → CTACAG or CTGCAA this could be done.

LacI-negative E.coli

To make the lac-system work we should use a strain that is lacI-negative. According to [http://partsregistry.org/Part:BBa_K177038 another iGEM group] the strain Top10 is lacI-negative.

Friday 1/7

mCherry insert and pLac backbone was isolated from gel using Quiquick Gel Extraction kit and then ligated using the following reaction mix:

The ligation mix was ligated at 16C for 1 hour.

Ligation mix was then transformed to LA + Amp, LA + Amp + IPTG and LA + Amp + more IPTG

Two new biobricks were also transformed and plated out on LA + Amp:

Monday 4/7

Plasmid isolation of GFP, RBS and LacP+mCherry. Concentrations were measured.

Gel picture of the separated fragments resulting from the restriction cutting of the biobricks "GFP" and "RBS". The squares indicate the fragments that where cut out of the gel

Restriction cutting of RBS and GFP:

• RBS: SpeI and PstI making it the backbone
• GFP: XbaI and PstI making it the insert.

Gel Extraction:

Extracted RBS backbone, and GFP insert form the gel.

Plating:

Plating of pLac + mCherry on amp plates, amp plates with additional IPTG (7µL), amp + IPTG plates and amp + IPTG plates with additional IPTG (7 µL). Incubating on 30 and 37 degrees.

Tuesday 5/7

Ligation of RBS backbone and GFP insert.

• 10μL Ligation Mix
• 1.0 μL 10X T4 ligase buffer
• 6:1 molar ratio of insert to vector (~10ng vector)
• Add (8.5 - vector and insert volume)μl ddH2O
• 0.5 μL T4 Ligase

Used 2,5 µL RBS backbone and 6 µL GFP insert. Incubating at 16 degrees celsius, then heating at 80 degrees celsius.

PCR amplification of rrnB P1 from BioBrick

Resuspend primers in dH20. Primers will amplify the whole rrnB P1 BioBrick (rrnB.FWD and REV), and only the assumed promoter sequence (pro.FWD and REV), and will add normal prefix and suffix instead of BBb format.

Primers used:

PCR mix:

Work on ice

• Dillute P1 DNA 1µL + 9µL dH2O → ( 9,84 g/µL P1 DNA)
• 2 x PCR tubes 0,5 µL DNA
• 5 µL 10x PCR buffer 2 (w/MgCl)
• 0,5 µL 10 mM dNTPs
• 1 µL fwd primer (rrnBL og proL)
• 1 µL rev primer (rrnBL og proL)
• 0,5 µL polymerase
• 41,5 µL H20

Heat cycles:

Heated lid 103C

• Initial denaturation: 94C 2 min
• Denaturing: 94C 30 s
• Annealing 58C 30 s
• Elongation 72C 60 s
• Repeat 2-4 34 times
• Final elongation 72C 7 min
• Cooling 4 C HOLD

Running products on 1,5 % agarose to find short fragment (promoter sequence). Should give 552 bp (rrnB) and 129 bp (proL). The products were not so good, so we are running a new PCR tomorrow with different scheme.

Inoculated "LacI with RBS", TERM and LacP+MC biobrick. LacP+MC with and without IPTG and incubating at 30 and 37 degrees celsius.

Wednesday 6/7

Running PCR with rrnBS and L and proS and L on the rrnB P1 BioBrick. 5 cycles of 58C annealing temp, and 20 cycles of 68C annealing temp to try adjust for the massively changed annealing temperatures when primers with pre- and suffixes bind to PCR products. The PCR products where separated by gel electrophoresis and cut out, ready for gel extraction tomorrow.

Isolated plasmids containing the "LacI with RBS" and "TERM" biobricks.

Gel picture of the separated fragments resulting from the restriction cutting of the biobricks "LacI with RBS" and "TERM". The squares indicate the fragments that where cut out of the gel

Restriction cutting of "LacI with RBS" with EcoRI and SpeI, and "TERM" with EcoRI and XbaI. The fragments where separated using gel electrophoresis.

The "LacI with RBS" insert and the backbone containing "TERM" where cut out of the gel, and extracted from it.

RBS+GFP transformants where inoculated in 3 mL LB+amp.

Thursday 7/7

Ligation of TERM backbone and LacI with RBS insert extracted from gel 6/7.

10μL Ligation Mix:

• 1.0 μL 10X T4 ligase buffer
• 6:1 molar ratio of insert to vector (~10ng vector)
• Add (8.5 - vector and insert volume)μl ddH2O
• 0.5 μL T4 Ligase

Used 2,5 µL TERM backbone and 6 µL LacI with RBS insert. Incubated at room temperature for 30 minutes, then heated at 65 C for 15 minutes.

• Plasmid with GFP+RBS was isolated. Concentration was 26.7 ng/µl

Restriction cutting:

rrnB P1 BioBrick

PCR products from rrnB P1 BioBrick separated on 1.5 % agarose. The marked products represent rrnB P1 with regular pre/sufix, and the promoter sequence w. pre/suffix

The rrnB P1 BioBrick found in the distribution was in a different format (BBb), and was therefore not compatible with the other BioBricks we are using. PCR was used to amplify the BioBrick itself, adding the prefix and suffix found [http://openwetware.org/wiki/Synthetic_Biology:BioBricks/Part_fabrication here] making it compatible with the other parts, but losing the first 10 bp. We also amplified only the assumed promoter sequence, with the pre/suffixes.

Gel electrophoresis with the PCR products showed that DNA of the right sequence length had been amplified, as shown in the figure. The full-length rrnB P1 amplicon had an approximate size of 500 bp, and the shorter promoter-only amplicon was approx. 100 bp. The shorter fragments shown were created using shorter primers with only X and S restriction sites, in case the long primers failed.

The amplicons with the complete pre/suffixes were cut out, as shown in the figure, and purified with QIAquick Gel Extraction Kit.

Both promoter variants were cut with E and P and also with E and S to create insertable pieces. Our RBS+GFP BioBrick was cut with E and X to create a backbone, and the linearized backbones psB1A3 and psb1C3 were cut to accomodate the cut PCR products.

Friday 8/7

It's Friday, we excited...

- The following ligations were made:

RBS + GFP insert fragments are shown in the black box.

- RBS + GFP was cut with Xbal and PstI, and the restriction fragments were separated on agarose gel. The insert fragment RBS + GFP were as expected (ca 750 bp), and the fragment was cut out from gel and extracted by using DNA gel extraction kit. The DNA concentration of RBS + GFP insert was measured to 2.1 ng/µl.

PCR amplification of relA from chromosomal DNA

Resuspend primers in dH20. Primers will amplify the whole relA gene from E. coli and add normal prefix and suffix (biobrick standard).

Primers used:

PCR mix: Same as used earlier.

Heat cycles:

Heated lid 103C

• Initial denaturation: 94C 2 min
• Denaturing: 94C 30 s
• Annealing: 58C 30 s
• Elongation: 72C 150 s
• Repeat 2-4 4 times
• Denaturing: 94C 30 s
• Annealing: 68C 30s
• Elongation: 72C 150 s
• Repeat 6-8 19 times
• Final elongation 72C 7 min
• Cooling 4 C HOLD

PCR products where put in the freezer for further work tomorrow.

Saturday 9/7

Transformed new promoter system for our relA gene from biobrick plate and plated out on Kam plates:

Changed medium for our TOP10 culture

Separated PCR products of the relA gene on gel and used QIAquick Gel Extraction Kit for cleanup. Concentration: 3 ng/µL

Monday 11/7

The new relA biobrick was digested with EcoRI and PstI for insert in plasmid backbone pSB1A3. The following reaction mix was used:

• 17 μl DNA
• 2 μl buffer 3
• 1 μl EcoRI
• 1 μl PstI
• 0.5 μl BSA
• Incubation on a 37 °C water bath for 30 min
• Heat kill (80 °C for 20 min)

Then the digested relA was ligeted with linearized pSB1A3 using the iGEM procedure for ligeting linearized plasmid backbones. The procedure can be found [http://partsregistry.org/Help:Protocols/Linearized_Plasmid_Backbones here].

pSB1A3 containing relA was then transformed to competent DH5 α cells and incubated overnight.

Gel picture of the separated fragments resulting from the restriction cutting of the biobricks "rrnBL in pSB1A3 plasmid" and "RBS+LacI+TERM". The squares indicate the fragments that where cut out of the gel

Plasmid Isolation:

Restriction Digestion: Digested rrnBL in pSB1A3 with SpeI and PstI and the LacI construct (RBS+LacI-TERM) with Xba1 and PstI

Tuesday 12/7

- Colonies from TOP10 plates were transferred to new plates with LA and LA + Kan to check wether the cells had lost their plasmid or not.

Since the first GFP biobrick we tried did't work properly, we transformed two new variants of GFP. In addition, we also transformed the biobrick coding β-galactosidase, to be able to measure activities of different promotors by setting the promotor in front of the β-galactosidase biobrick, induce the promotor, destroy the cell and look at the absorbance when we add for example x-gal, or other molecules that give coloured components when cleaved with β-galactosidase.

Sponsors

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NTNU Rector's Office Programme for Bioinformatics, NTNU