• Introduction
  • Home
  • The Team
  • Photo Gallery
• Our Project
  • Results Summary
  • Selection System
  • In-Vitro Characterization
  • In-Vivo Characterization
  • Microfluidics
  • Data
  • Attributions
• Tools
  • Gibson Assembly
  • MITOMI
• Notebook
  • Protocols
  • May
  • June
  • July
  • August
  • September
  • October
• Considerations
  • Human Practices
  • Safety
• Acknowledgements
  • Sponsors
  • Partners

Notebook: July 2011

Friday, 1st of July 2011

Alina and Lilia did MITOMI on His-tetR expressed from linear template, it was loaded on chip in ITT expression mix. DNA was spotted on June 29 in different concentrations for both: consensus (tetO1) sequence and a random sequence ((-)control).

Images: Green fluorescence comes from green-lysine and red fluorescence comes from DNA (cy-5 labeled).

Although we don't observe much protein bound to the anti His-tag antibody, we can still see that it does bound TetO1 sequence and did not bind any (-)control sequence. Some possible reasons for low protein fluorescence under the buttons: the expression yield from the linear template with T7 promoter might be too low, the His-tag to antibody binding is not strong enough or the concentration of antibody is too low.

Friday, 1st of July 2011

Alina and Lilia amplified the His-tetR linear template. After PCR sample was loaded on 1% agarose gel with Rad Safe, “1Kb Plus DNA Ladder” was used.

We also prepared about thirty LB-agar plates with ampicilin, they are in the BM fridge.

Colonies from Gibson

After an overnight incubation, we found four colonies on the Ampicillin plates that had cells containing the plasmids from the Gibson assembly. The low number of colonies is attributed to the low competence of the cells. Of the four colonies, two were pink and two were yellow.

Tween experiment

Clara and Henrike tested the right dose of Tween 20 that can be used for the "chemostat" experiment without affecting the cell growth. Tween is a detergent that would prevent the cells from sticking and thus clogging the microfluidic channels. We tested 12 different dilutions of Tween 12 both for GFP and RFP e-coli which can be potentially used for the "chemostat" experiment. We read the OD(absorption @600nm) and fluorescence every 10 minutes, for 18 hours at 37°C.

Growth curves for all the different concentrations vs time

The legend shows the percentage of tween 20 that was added to the medium.

• We can observe that the growth factor is smaller for Chloramphenicol resistant e-coli due to the fact that Chloramphenicol is stronger than Kanamycin.

Calculated growth factor for the previous curves(Lilia)

Growth factor

We can observe that tween did not have a major effect on the cells' growth. I suggest we use 0.075% tween in media for the experiments

Monday, 4th of July 2011

Alina and Vincent made plates (large and small) with chloramphenicol (concentration of 34 mg/mL). We used .74 mL of chloramphenicol for a liter of LB agar and plated them directly under the flame.

To figure out what was going wrong with the P23019 plasmid, we used the Nanodrop to determine that the sample (Plate 4, well 14E) was at a concentration of 97.4 ng/microL. This result seemed to indicate that there was DNA in the sample of the plate (as opposed to just red dye without DNA).

Tuesday, 5th of July 2011

Since we were running out of the P23019 plasmid DNA to try new PCRs, we thought it would be a good idea to transform it. We used both Lilia's and Alina's cells, adding a negative control. The incubation for chloramphenicol required a two hour recovery period in the incubator, since the antibiotic is stronger. After Tuesday's meeting, we went ahead and plated the result and let the plates incubate overnight.

Meanwhile, moving on with the Gibson assembly of the J61002 plasmid, Vincent tried to obtain the final Gibson sequence. This sequence would be used to see if PstI and SpeI would cut differently on the assembled plasmid versus the normal J61002 plasmid: we hoped this would allow us to check that Gibson had worked successfully if we ran the ligated plasmids on a gel. Ideally, the J61002 original plasmid would cut at two locations while the Gibson plasmid would only cut in a single location (the biobrick scar would make it impossible to cut at the previous cut location). On a gel, we would see a single piece of about 3000 bp for the Gibson plasmid and two bands of approximately 2200 and 700 bp respectively for the normal plasmid.

Using the plates with the four Gibson colonies, Vincent made cultures which he put in the incubator overnight.

Wednesday, 6th of July 2011

With the Gibson cultures in hand, Vincent made glycerol stocks (500 microL glycerol, 500 microL cells) and then mini-prepped the four cultures using the standard protocol. The resulting DNA plasmids were ready for enzyme ligase.

Vincent also looked at the results of the transformation of the P23019 using two different sets of competent cells and negative controls. No colonies grew, leaving us quite perplexed as to what was in the original P23019 well. Determined to find a substitute for the P23019 plasmid that would serve as a vector for the TetR sequence, we searched through the database looking for a plasmid with resistance to something other than ampicillin as well as a P15a origin of replication. We found four distinct possibilities, only two of which were available in the plates from the standard registry: pSB3K1 which has kanamycin resistance, and pSB3C5 which has chloramphenicol resistance (very similar to p23019).

Thursday, 7th of July 2011

Vincent and Nadine made a digestion on the minipreps from the 4 colonies that were transformed with the Gibson-extended J61002 plasmid. If Gibson was successful, only Pst1 will cut and we should have one band of 3094 bp. If Gibson didn't work, then Pst1 and Spe1 will cut and we should have 2 bands of 890 and 2060 bp. The digestion was made according to last year's protocol, with 1.5 hour incubation. The ladder on the gel is 1kb.

Colonies 1 and 4 have the expected band over 3kb, which is coherent with the observation made that they did express RFP. But colonies 2 and 3 have only one band... It is likely that in these cells the plasmid recombined in a shorter way, without RFP but with the resistance; otherwise the plasmid sequence is not what we think. We'll check tomorrow on the J61002 plasmid if we do get 2 bands on the starting plasmid. Also, we have some light smaller bands in colonies 1 and 4, indicating that the miniprep is perhaps not so pure.

Vincent and Alessandro transformed the J61002 original plasmid, since we were running out of DNA with which to compare to the Gibson assembly. In addition, they transformed the results of the previous day's registry search for convenient substitute plasmids (for p23019) using Alina's cells using 50 ng/microL concentration (Chloramphenicol Chl-SB3C5 70.6 ng/microL, K-SB3K1 67.7 ng/microL). These were plated appropriately and put in the incubator overnight.

Lilia and Alessandro did a MITOMI experiment on deBrujin sequences. Non of the sequences showed up to be bound nicely. But the protein pull down was not so robust due to the surface chemistry problems... Experiment needs to be repeated.

Friday, 8th of July 2011

Thanks to Henrike's expert eyes, we were able to harvest many colonies from the chloramphenicol pSB3C5 plasmid as well as many for the J61002 plasmid and the kanamycin plasmid. Since the chloramphenicol plasmid seemed closest to the p23019 plasmid for which we already had primers, it made sense to pursue the Gibson strategy for that plasmid. Alessandro and Vincent made culture tubes and put those in the incubator overnight. In the meanwhile, primers were designed for the next phase of Gibson assembly (i.e. the new pSB3C5 plasmid with the old TetR piece).

Gel from the tetR mutants PCR. 1000kb ladder.

We ran the PCR on the tetR linear template, using Clara's primers for site-specific mutagenesis.

Six PCRs were run. The first amplified the common sequence of the mutants: everything up to the mutated sites. The six other reactions amplified the second half of the gene, inducing specific mutations in tetR.

The fluorescence traces are insufficiently clear for accurate conclusions, therefore the PCR and gel will be repeated with different concentrations on Monday.

Saturday, 9th of July 2011

Vincent came in to pick up the J61002, pSB3C5, and pSB3K1 cultures from the incubator. He found that all the J61002 cultures were pink (as expected since they have the RFP gene). Both kanamycin cultures were pink, and two of the three chloramphenicol cultures were pink (though not as strong a pink as that of the J61002 plasmid). He went ahead and mini-prepped all the cultures, using hot water (55 C) instead of warm TE buffer during the elution step. He then made glycerol stocks (50% cell, 50% glycerol) and placed them in the -80 freezer. Finally, he measured the concentration of the resulting DNA after the mini-prep:

pSB3C5, colony 1: 35.2 ng/microL (accidentally used 2 microL, vs. 1 microL so more diluted)

pSB3C5, colony 2: 78.4 ng/microL

pSB3C5, colony 3: 70.2 ng/microL

pSB3K1, colony 1: 15.5 ng/microL

pSB3K1, colony 2: 14.3 ng/microL

J61002, colony 1: 54.2 ng/microL

J61002, colony 2: 74.3 ng/microL

J61002, colony 3: 45.9 ng/microL

Monday, 11th of July 2011

Nadine made a PCR to prepare next Gibson assembly, ran it on a gel and recovered the according fragments from the gel. Details of the 4 PCRs:

• ColE1 backbone with Ptet (from newly assembled J61002 plasmid), final concentration: 15.1 ng/ul
• LacI ssrA rrnB T on repressilator plasmid, final concentration: 46.7 ng/ul
• T4 lysis cassette on registry plasmid, final concentration: 29.7 ng/ul
• RFP amplification with Plac from Gibson J61002 plasmid, final concentration: 61,2 ng/ul

Alessandro made again a digestion on the 4 colonies recovered from last Gibson assembly, with this time also the original J61002 plasmid. See Thursday 7th July for more details. This confirms that colony 3 has somehow reassembled without RFP because it is smaller than colonies 1 and 4. The bands are bigger after digestion because the plasmids have become linear and they run slower than the coiled plasmids.

Tuesday, 12 July 2011

Douglas obtained satisfactory amounts of product from the mutation PCR on the tetR linear template. The most successful one required 1 uM of primers, mixed to the 100x diluted template (0.327 ng/uL concentration).

Gel from the first successful variants PCR. Codes indicate the point mutations.

Again, seven PCRs were run. The first copies the common sequence, up to the mutated bases in the tetR coding region, with some padding (illustrated above). The next six copy the remaining sequence, and induce these specific mutations:

1. VF 36
2. EA37
3. PK39
4. YF42
5. PQ39YM42
6. PQ39LV41M42

The gel fluorescence traces show what appears to be PCR product in large amounts for the Common and EA37 reactions, and smaller amounts for the YF36 and YF42 reactions. The remaining three show almost no activity.

The PCR products were subsequently separated using gel electrophoresis then cut out. They will be purified tomorrow.

Nadine made 2 Gibson assemblies with the PCR products form yesterday, transformed cells and plated them on ampicillin dishes. The newly assembled vectors will have ampicillin resistance, LacI under Ptet plus either lysis under Plac or RFP under Plac.

Wednesday, 13 July 2011

First result from the fusion PCR: tetR mutant EA37 appears in "detectable" amounts

Douglas purified the gels containing yesterday's mutation-PCR products, following the XXX protocol XXX. Isopropanol was added to the "Common PCR" product, as its expected length is inferior to 500bp. The final DNA concentrations, measured by photospectrometry, are listed in the following table. Even the very low concentration of YF36 should be sufficient for a PCR template, and the weird "260/280" ratio apparently results from agarose gel residues.

These sequences were then used for a fusion PCR, to stitch mutants YF36, EA37, and YF42 to the common sequence, according to the protocol *To be written*. Only the EA37 mutant, which was also the brightest on the PCR gels, yielded a significant amount of product. The next step is to check the product is the desired mutant, in order to confirm the success of this method. We also have to refine the PCR to get the other mutants to work; it seems the problem comes from the primers' melting temperature.

Alessandro and Nadine autoclaved beads and prepared 4 bottles of SOC medium. We took the plated cells (J61002 Ptet-LacI Plac-lysis & Ptet-LacI Plac-RFP) from incubator and put them in suspension (LB medium + ampicillin) to grow overnight. We also plated the rest of these transformed cells. We did a Klenow reaction on the 1off library to have dsDNA. The ordered plasmids arrived,so we made a PCR on pSB3C5 (to amplify the backbone) and on TetR (adding pConst) to prepare the parts needed for Gibson.

Thursday, 14 July 2011

J61002 plasmids

Alessandro made minipreps on cells grown overnight and made glycerol stocks of them (500 microL). Because the cells that we assume to have RFP (under the control of Plac) are not a little red, we also kept an aliquot of these cells to make a test with IPTG (this is a molecular mimic of allocaltose therefore it triggers the transcription on Plac): if these cells become red with IPTG we can be sure that RFP is controlled by Plac in our plasmid (from Gibson assembly).

Alessandro digested the plasmind (from miniprep) with PstI because Nadine found that if the Gibson went well, they should have 2 restricition sites for this enzyme - instead of 1 for J61002 Ptet-RFP plasmid. Unfortunately, the results show that GIbson didn't work... For every colony we have a band at 2.5 kb, which corresponds exactly to the size of the backbone.

The backbone must have closed without the inserts... We can redo Gibson with less backbone. On the plates we prepared yesterday one colony is red! We suspended it, we'll check tomorrow if this one has the correct plasmid.

pSB3C5 plasmid

pSB3C5 backbone purification, both bands contain the same product.

The PCR to add Pconst to TetR didn't work, but we already have it in the freezer. Nadine purified the pSB3C5 backbone, but the bands on the gel were really weak even with all the PCR products loaded onto the gel and the concentration is only 6 ng/ul. We will anyway try Gibson tomorrow...

tetR mutants

Douglas designed primers for site-specific mutagenesis of tetR, following the protocol protocol. We are testing this as another approach to inducing mutations. The primers were designed for the same mutations as attempted by extension PCR, i.e.:

1. V36F
2. E37A
3. P39K
4. Y42F
5. P39Q_Y42M
6. P39Q_L41V_Y42M

By laziness For convenience, the primer codes were changed to match those used by Agilent's primer design software. For example, V36F indicates a substitution of amino acid F for V in position 36.

Friday, 15 July 2011

The IPTG test gave us bad results (as expected due to data came from digestion): no increase in RFP and no decrease for the T4 lysis cassette. Alessandro made miniprep and started the digestion for the only one red colony that he inoculated the day before.