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Team:Grenoble/Notebook/July
From 2011.igem.org
July 7th to 13th
Biology
Moving in to the CIME, a biology teaching platform, free for the summer vacation. Preparation of new storage. PCR results from last week cloning.
- Moving in of the whole team to a new lab
- Cheking of DNA concentration into our Biobrick Miniprep :
- Order of new enzymes from New England Biolabs Company
- PCR Checking of cloning from the last week
- Making new storage
- RBS-TetR Miniprep
We are taking advantage that the school year is over to move in the CIME, a teaching platform of biology.
OD cheking was performed on all our Biobrick stock to have an idea of the DNA rate into our preparation. We also made a PCR cheking to make sure that the DNA rate really corresponds to our Biobrick. We got an average rate of 100 ng/µl. Which is a much lower than expect, so 10 times more DNA products would had been necessary to get great constructions.
We hope to increase the digestion efficiency.
As previously, inserts were shorter than expected, except the construction RBS-TetR.
Petri Dishes with Antibiotic (Amp, Kan, Cm, Tet). LB Culture medium
In order to send it to the sequencing.
Biology
Miniprep of pTOPO clones to check for the presence of insert. Digestion with EcoRI and PstI. One clone is sent to sequencing for : fhaSL ; rsmA protein coding sequence, rsmY regulatory RNA. Adaptation of a new transformation protocol (by electroporation), given by some other members of our group.
Second try of inserting our sequences into an Igem plasmid from PCR products, and first 3A ligation:
- fhaLS + gfp on PSB1C3
- rposLS + gfp on PSB1C3
Modelling
Learning Gillespie and looking for parameters.
- Models :
- Parameters :
Stochastic model is on its way. We base it on Gillespie's algorithm. It's mainly about getting familiar with the math for now. Also working on Hysteresis and isoclines subparts of the deterministic models.
Still a lot of work going on there. The problem is we can not compare our sets to experimental results as the whole system is not finished yet. We will then try to characterize some of the promoters we use and figure out how to obtain some degradation rates as well.
July 14th to 21st
Biology
Better clonings rate: Clonings performed with recommended enzymes by iGEM.
- Stock of electro competent cells :
- Results :
- New stock of Biobrick Miniprep :
- Cloning (Standard Assembly Method) of every first steps of our construction :
- 11 clonings
- Cloning session :
- Every 1st-step constructions that failed last time, so 6 constructions.
- 2 2nd-step constructions :
- MerR-LuxR
- TetR-LuxR
Great transformation rate
DO checking, PCR cheking
We changed our strategy: clonings were performed with enzymes recommended by iGEM ().
One Petri Dish was free of colony. We performed PCRs on 5 colonies from each Petri Dish. According to PCR results, 5 constructions out of 11 seem to have the right size.
Only digestions were performed because of a lack of equipments. We decided to use the Standard Protocol for the first step constructions because the assembly combinates a short and a long gene. The long gene is inserted in the plasmid of the small gene. But the Second step constructions were performed with the 3A Assembly Protocol.
Modelling
Stochastic model done.
- Models :
- Parameters :
First results with the stochastic model. Our whole model does work like we expected it. But parameters are needed more than ever now.
We got incomplete sets of parameters from either litterature or iGem teams. Some very useful sets can be found in Aberdeen 09, Brown 10, ETHZ 07, BCCS Bristol 08.
Biology
Production of Bba_J23119, a constitutive promotor needed in our construction : transformation of cells, selection of some clones, digestion, migration on accrylamid (better vizualisation of small fragment) agarose gel to check for the presence of insert.
Second try to transform ligation from 28th June in Top10 super competent cells. Constructs were fha1SL-I13401, rposSL-I13401, fhaLS, rpoSLS, rsmA and rsmY ligated into pSB1C3. A first screen was performed on white colonies by colony PCR. Plasmid purification from positive clones and screen by EcoR1 and Pst1 restriction digest was done.
July 22nd to 27th
Modelling
Stochastic model done.
- Models :
- Parameters :
Stochastic program is implemented for the toggle switch and works fine. We adapted the program for the whole system so we can implement the quorum sensing stochastic model very quickly when we have the parameters (about 1/2 day of work). The current model and parameters prove that we do have a bi-modal distribution when IPTG and pollutant concentrations are equal :
On the X-axis we can see the concentration of lacI (neg) or merR (positive) in cells. On the Y-axis we can see the amount of cells in one way or another.
We have coherent sets of parameters, but we still can't compare our models to the real system and are waiting for the results of characterization experiments.
Biology
The first sequencing results are received: fha1LS and rsmY on pTOPO are OK. The rsmA coding sequence has a deletion. Realization of glycerol stock for the positives clones. Amplification with high fidelity Taq polymerase of rsmA and rpoSLS. Digestion and ligation of PCR products with I13401 (gfp) in PSB1C3 linearized plasmid. Three A assembly for :
- rpoSLS- I1340- pSB1C31
- fhaLS-I13401-pSB1C3
When screening transformants by PCR using VF and VR, DNA fragments appear to have the wrong size. Plasmid purification from positive clones and screen by EcoR1 and Pst1 restriction digests was done. 10 clones for construct 15 and nine for construct 14 were selected to check if leader sequences are upstream the I13401 (Leader sequences are too small to be seen on agarose gel.)
Flow cytometry comparison of the biobrick parts to our constructions:
- Bba_K256003 (Pcons-rbs-gfp)
- Bba_K176005 (Pcons-rbs-gfp) the twin of Bba_K256003
- Bba_E0840 (rbs-gfp), negative control
- Bba_13401 (gfp), negative control
Biology
Moving in to the CIME, a biology teaching platform, free for the summer vacation. Preparation of new storage. PCR results from last week cloning.
- Cloning session :
- every 1st-step constructions that failed last time, so 6 constructions.
- 2, 2nd-step constructions :
- MerR-LuxR
- TetR-LuxR
- Ligations :
- 1 vector/1 insert
- 1 vector/2 inserts
- 1 vector/3 inserts
- Transformations with electrocompetent cells
- Spreading over Petri Dish
- Results :
- Sequencing Order
- Products Order
- Cloning Session :
- 5 constructions with Fha1
- 3, 2nd-step constructions
- LacI-LuxI
- MerR-CinR
- TetR-CinR
- 1 construction for the tests
- pLux-GFP
- 1st-step construction
- RBS-CinI
- Results :
Because we still have a low cloning rate we tried different proportions between vectors and inserts:
Best results on Petri Dishes with the proportion 1/3. All constructions seem to have the right size except MerR-LuxR.
RBS-TetR RBS-LuxI RBS-CinR RBS-LacI pLac-GFP pCin-GFP pMerT-GFP pLux-Lyco
For ligations, digestions, PCR, MiniPreps, MidiPreps
The final RBS (Fha1) which allows to keep the toggle off has just been delivered. So, all first steps constructions including RBS were made once again. Because the efficiency of Fha1 hasn't been completly demonstrated, we keep on cloning with the standard RBS. So, RBS and Fha1 constructions are made in parallel.
Every constructions gave colonies on Petri Dishes. But PCR cheking showed that nothing were amplified on every Fha1 constructions with VF2 and VR primers. Thus, Fha1 was provided in a PCR blent plasmid instead of an iGEM's plasmid. The insert of the test construction is having the right size. 2 out of 3 2nd step constructions had the right size. We still have issues to clone the 1st step construction: RBS-CinI.
July 28th to 3rd
Biology
Constructs 14 and 15 are digested by Nco1 (cut into rpoSLS) and Ara1 (cut into fhaLS) in order to check for the presence of leader sequences. Negative results.
New PCR of rsmA, ligation in pTOPO and transformation. Screen of many colonies by PCR and mini prep. Test of different minipreping methods. The primers used for the screen are the same ones as the ones initially used to produce the amplicon. Incoherent results are given by the two methods. We deduce that the use of same primer set for amplify a sequence is not reliable for screening this same sequence on a clone in this case. Indeed, it is very likely to gives false positives.
Biology
According to the results from the sequencing order will have to start over constructions since the 1st-steps. A Purification step will be add for all 1st-step construction in order to get round our resistance issues.
- Cloning session :
- 1st-step construction: RBS-CinI
- 2nd-step constructions:
- TetR-CinR
- MerR-CinR
- MerR-LuxR
- LacI-LuxI
- 3rd-step construction
- pLac + TetR-LuxR
Digestions: Because we are having issues to get 2nd-step constructions. We tried both 3A Assembly and Standard protocols.
Cheking and purification gels: We add a cheking step, before performing ligations on Standard Protocol. To maximise our chance to get 2nd-step constructions, we tried to purified the inserts. On purification gel, plasmids seem to be digested but inserts is missing. On checking gel, cinI wasn't digested correctly.
- Sequencing Order :
- Results :
- Enzyme checking :
- Cloning session :
- Biobricks which require an RBS and have the same antibiotic resistance as RBS plasmid, were transfered on pSB1AC3 plasmid with chloramphenicol resistance :
- TetR
- LuxR
- LuxI
- LacI
- GFP
- Lycopen
- Fha1 was also transfered on pSB1AT3 plasmid to simplify selection of the right constructions.
- Digestions :
- Cloning session :
- 3rd-step construction :
- pLac + MerR-CinR
- pConst + MerR-CinR
- 2nd-step construction:
- RBS-CinI
- Preculture :
- Digestions :
- Purification :
- Ligations :
- Spreading over Petri dish
- Cloning Session :
- 1st-step construction START OVER :
- RBS-LacI
- RBS-TetR
- RBS-LuxI
- Fha-LacI
- Fha-LuxI
- Fha-LuxR
- Fha-CinI
- Fha-CinR
- Fha-TetR
- pLux-Lycopene
- pCin-Lycopene
- Construction Test :
- pCin-GFP
- pLux-GFP
- pTet-GFP
- pConst-GFP
- pLac-GFP
- pConst-RBS-CinR
- pConst-RBS-LuxR
- Digestions :
- Purification :
- Ligations :
- Spreading over Petri dish
- New stock on Petri Dishes :
- We spread again -80°C stock in order to start new miniprep of the troubling biobricks :
- Lycopene
- RBS
- Fha
- TetR
- LuxR
- LuxI
- CinI
- CinR
- pTet
- pMerT
- pCin
- pConst
- pLux
- Cloning Session :
- We started over constructions that couldn't be performed during the previous cloning because of wrong digestion :
- Fha-LuxR
- Fha-LuxI
- Fha-CinR
- Fha-CinI
- pCin-Lycopene
- pLux-Lycopene
- pConst-RBS-LuxR
- RBS-LuxI
- RBS-LuxR
- Digestions :
- Purification :
- Ligations :
- Spreading over Petri dish
RBS-TetR RBS-LuxI RBS-CinR RBS-LacI pLac-GFP pCin-GFP pMerT-GFP pLux-Lyco
6 out of 8 sequence alignments failed.
To perform this constructions, we used standard protocol: we kept the plasmid of the shortest biobrick which we inserted the longest biobrick. The problem was identified as coming from a wrong identification of antibiotic resistants. In most constructions below, vector and inserts had the same antibiotic resistance. So, even wrong constructions were selected on Petri Dishes.
Because we had no results with the latest cloning session, we tested our enzymes. We tried to digest each site individually. We obtained linearized plasmid. So, enzymes are well working.
A gel checking of the restriction results were performed.
Spreading over Petri dish
On the Restriction Gel, We obtain the right size for all inserts. Because pSB1AC3 is a double resistance plasmid (ampicillin and chloramphenicol) and RBS plasmid is on ampicillin, as previously the right constructions won't be selected.
To perform this new cloning session, we first selected 5 colonies from the Petri dish of MerR-CinR construction.
a gel checking of the restriction results were performed.
In order to check and extract the wright insert.
Standard Protocol was performed. MerR-CinR was inserted into pLac and pConst plasmids.
A gel checking of the restriction results were performed.
In order to check and extract the wright insert.
Standard Protocol was performed. MerR-CinR was inserted into pLac and pConst plasmids.
On Puritication gel, 4 biobricks were not correctly digested: CinI, LuxI, LuxR, RBS-LuxR. All the other were apparently well purified. Ligations were performed as usual.
Results on Petri Dishes were unsatifying: we obtained an agglomerate of colonies. And this in all Petri Dishes. Does the issue come from too old Petri Dishes? Or LB pre culture ? So, we tried a 2nd-spreding on Petri Dishes and the result was the same. We also checked by PCR if we could work anyway with those colonies. But the results were not conclusive.
A gel checking of the restriction results were performed.
In order to check and extract the wright insert.
Standard Protocol was performed. MerR-CinR was inserted into pLac and pConst plasmids. We add a control for the ligations: plasmids without its inserts (pLux, pCin, Fha, RBS).
Modelling
It's all about patience
- Models
- Parameters
Stochastic program is implemented for the toggle switch and works fine. We adapted the program for the whole system so we can implement the quorum sensing stochastic model very quickly when we have the parameters (about 1/2 day of work).
We have coherent sets of parameters, but we still can't compare our models to the real system and are waiting for the results of characterization experiments.
