Team:Toulouse-INSA-UPS/Notebook
NOTEBOOK
Here, you will find information about the temporal aspects of our project.
LABBOOK
To achieve our lab work, we splited into different teams, each working on different aspects of the experimental procedure. Three teams were then formed :
- Team Coli: this team was managed by Younes and included Marion. Their goal was to achieve the production and characterization of Cerberus and Sirius in Escherichia coli
- Team Pichia: this team was ruled by Angeline and included Gaëlle. Their mission was to reproduce the experiments planned on Escherichia coli in Pichia pastoris
- Team Biotin: this team was ruled by Amandine and included Jean and Julien. Their objective was to construct and to test our in vivo biotinylation system.
- Team Callulose: This team was managed by Cal (so the Callulose name) and got help from Younes. Its mission was to launch and optimize our bacterial cellulose production.
LABBOOK: JUNE
18/06 -> 22/06 :
For the first week in the lab, we recovered and amplify our plasmids (pPICz, pETDuet, pET28, pGAP) but also our bacterial strains E. coli BL21 DE3 and Tuner.
25/06 -> 29/06 :
- Team Coli: we started with a PCR on the the gblocks Cerberus-pastoris. In order to clone this gblocks, we prepared the pGAP plasmid by amplifying it in E. coli Stellard cells before a Midiprep. Another aspect was to check the pREAV which will allow the incorporation of a unnatural amino acid in our Cerberus.
- Team Pichia: pPIC, pGAP and pETDuet were good but pPIC did not correspond to our expectations so we had to find another solution
LABBOOK: JULY
02/07 -> 06/07 :
- Team Biotin: this week, we have done BirA PCR and we had digested the pPIC after his amplification in E. coli Stellard cells. This allowed us to do our first cloning with BirA in the pETDuet. We have checked the clones by digestion and they were OK. It was necessary to sequence this clones before doing the next cloning in pETDuet. We found another pPIC and we checked it.
- Team Coli: this week, it was the first In-fusion cloning with our Cerberus in the pET28. We used two differents construction for Cerberus, one with a monomeric streptavidin and another with a tetrameric streptavidin. Then, we checked the construct by digestion before sending it for sequencing. In the same time we checked our plasmid pEVOL-azF which allow the unnatural amino acid incorporation in E. coli.
- Team Pichia: this week, we did the In-fusion cloning of Cerberus-strepta in pGAP with the material prepared the week before. So we had to check some clones by digestion before sequencing. Fortunately, they were good. It was also this week that we received the GS200 strains cell.
09/07 -> 13/07 :
- Team Biotin: on monday we sent our pETDuet BirA clones obtained last week to sequencing and we were happy that our clones were validated. In the same time, we carried on the PCR with the parts that will serve us to functionalise our Cerberus after biotinylation by BirA.
- Team Coli: This week, we received the sequencing results for Cerberus and it was again a successfully cloning for the Toulouse iGEM team. We cloned Sirius (CBM3-RFP) in the pET28 with the In-fusion kit. To do this, we performed PCR on the gBlocks then we used the In-fusion kit. After verification, Sirius was OK.
- Team Pichia: we checked the pREAV and found out the plasmid map didnât correspond with our digestion results. We needed to find another pREAV...
16/07 -> 20/07 :
- Team Biotin: This week, we focused on the Pastoris cloning. In one hand, we prepared the pGAP vector (amplification, purification and digestion), mRFP1, BFP and Sygonadine parts and we did the three cloning. We tried to amplify and purify pPIC but unfortunately it was necessary to try again because the Midiprep didnât succeed.
- Team Coli: this week, we made or own competent cells using BL21 and tuner strains
- Team Pichia: this week, we did In-fusion cloning in the pGAP but this time with the cerberus mSA2. After transformation, culture and miniprep, we checked clones by digestion. The cloning was a success.
23/07 -> 27/07 :
- Team Biotin: this week, before another midiprep, we checked the pPIC but we still had a mapping problem. After many verification, it was clearly not good but we found another source for this plasmid and it seemed OK. We amplified it by midiprep.
- Team Coli: this week, we did the first production assay for Sirius and we were very happy because we obtained a red culture medium.
- Team Pichia: this week, the pichia team helped the other teams because it was ahead of the planning and had to wait for yeast growth.
30/07 -> 03/08 :
- Team Biotin: this week, we worked on pETDuet-BirA to clone our functionalising proteins (mRFP1 and BFP). We amplified the pETDuet-BirA and after Midiprep and digestion, we cloned mRFP1 and BFP with the In-fusion kit. After digestion, we sent clones to sequencing and started production assay in E. Coli BL21.
- Team Coli: we did the first Sirius purification after production in E. coli BL21. To do this, we used an IMAC column and dialysis. In order to proved the CBM3 fixation to cellulose, we prepared the regenerated amorphous cellulose.
LABBOOK: AUGUST
06/08 -> 10/08 :
- Team Biotin: this week, we worked on the production assay for biotinylated proteins in E. coli. Furthermore, we cloned BirA in the pPIC plasmid and we checked it by digestion and sequencing. After that, we cloned RFP, Sygonadine and BFP in this plasmid to produce the proteins in Pichia pastoris.
- Team Coli: in order to show the efficiency of the second Cerberus head, we needed a Cerberus which has just its CBM3a head and the streptavidin head. We did a directed mutagenesis on the stop codon to create Orthos.
13/08 -> 17/08 :
- Team Biotin: we produced biotinylated proteins with E. coli, with and without biotin in the culture medium.
20/08 -> 24/08 :
- Team Coli: this week was a particularly busy week. We did the Orthos production and purification but also the same for Sirius and mRFP1. This allowed us to perform a cellulose pull down assay with Sirius and mRFP1 as a negative control. In addition, we did the production of Cerberus. To do this, we did co-transformation of BL21 cells with pET28 Cerberus and pEVOL AzF. The cell culture medium was complemented with with AzF unnatural amino acid to allow its incorporation. Cerberus was purified by a cellulose pool down assay.
- Team pSB1C3: we created this new team to start the pSB1C3 clonings. PCR was performed on our gblocks. Unfortunately, we didnât succeed to amplify all the gblocks.
27/08 -> 31/08 :
- Team Coli: in order to demonstrate the efficiency of the third Cerberus head, we did a click assay with fluorescein DBCO.
LABBOOK: SEPTEMBER
03/09 -> 07/09 :
- Team Coli: in order to demonstrate the efficaciency of the AzF head, we tried to click paramagnetic beads on it. The aim was to see the displacement of the cellulose when in a presence of a magnet
- Team pSB1C3: this week, we tried again the pSB1C3 clonings. We used another pSB1C3 and tried a classic cloning with restriction enzymes instead of In-fusion. At the end of the week, we sent our pSB1C3 to sequencing.
10/09 -> 14/09 :
- Team Biotin: we successfully made a pull down assay with Orthos to measure the BFP fluorescence with and without Orthos on cellulose.
17/09 -> 21/09 :
- Team Biotin: this was the final assay and we proved the fixation of the biotinylated BFP on cerberus.
24/09 -> 28/09 :
- Team coli: This week we did our last manipulation to show that we can fix BFP-DBCO to the head streptavidin
NOTEBOOK
NOTEBOOK: FEBRUARY
February 1st, 2018: Kick-off meeting
Gathering the team members, distribute the tasks and of course get to know each othersâŚ
The iGEMâs adventure begins!
February 8th-22nd, 2018: Brainstorming
At the beginning, more than 50 ideas were proposed. The most original ideas were selected during our brainstorming sessions.
At the end of the month, still 11 subjects need more investigations.
February 21st, 2018: Escape game conference
We attend a conference organized by the Catalyseur on the creation of a teaching escape game. We met two professors in high schools option âSciences and technologies laboratoryâ.
NOTEBOOK: MARCH
March 1st-15t, 2018: Brainstorming
Only 5 subjects still in course!
March 10th, 2018: Grimoire
At this event we introduced our card game Microbioworld.
March 20th, 2018: CRISPR/CAS meeting
We meet a CRISPR/CAS expert in the LMGM lab who teaches us a lot about the new possibilities of the system.
NOTEBOOK: APRIL
April 5th, 2018: Final choice of our project
After a long period of brainstorming, we have decided to work on moleculesâ binding on cellulose. Now, we had to think of our projectâs name.
April 12th, 2018: Tour des Sciences
We still present the Microbioworld game during the âTour des sciencesâ.
NOTEBOOK: MAY
May , 2018:
We work on the design of the project with the help of our supervisors.
May 31th, 2018:
We met Philippe Serp and his team to manipulate our graphene on his lab.
NOTEBOOK: JUNE
June 18th, 2018: First day in the lab
We were all very impatient, and finally it has come! Itâs the first lab day.
June 19th, 2018: Fondation INSA Toulouse meeting
Looking for funding, we present our project to the INSA Toulouse fondation.
June 23rd-24th, 2018: Collaboration with Montpellierâs team
We start a collaboration with the Montpellier team to help them in some areas like the wiki. To do this we go to Montpelier.
June 25th, 2018: TWB meet
We went to TWB, one of our main funders.
June 26th, 2018: NUS meeting
We organizing a skype with the NUS team to discuss about a possible collaboration.
June 27th, 2018: Meet with STL teachers
As part of our discussions with the ministry of education, high school teachers visit us.
June 27th, 2018
Entrep: We met Guillaume Boissonat, who co-funded the startup pili.bio. He advises us when creating our the business model.
June 29th, 2018: Primary school intervention
We intervened in a school in order to present Microbiolworld, the research profession, and more generally introduce the world of microbes.
NOTEBOOK: JULY
July 5th, 2018: CALMIPâs meet and visit
We visited CALMIP a high-throughput calcul center which allowed us to make complex calculations for our modeling.
July 6th, 2018: Official announcement of our project
We officially present our project on social media!
July 7th, 2018: 4th Annual Parisian Meet-up
We took part in the annual Parisian Meet-up organized by Pasteur iGEM team.
July 7th-12th, 2018: EuroScience Open Forum (ESOF)
We participated in the EuroScience Open Forum in Toulouse to introduce the iGEM competition and synthetic biology for the public.
July 19th, 2018: First publications in media
Toulouse media speak about us, we are very happy of this recognition!
July 20th-22nd, 2018: European Meet-up in Munich
Two members of the team travelled to Munich to represent our team.
July 30th, 2018: Incubator meeting
We met Yohann Bouvier who is the manager of a startup incubator. He advices us regarding our entrepreneurship approach.
NOTEBOOK: AUGUST
August 1st, 2018: Laval skype
We take contact by skype with the Laval iGEM team.
August 17th, 2018: Shooting photo for the wiki
We put out our nicest clothes to make the pictures used in our wiki.
August 25th-26th, 2018: Collaboration with Bordeauxâs team
We go to Bordeaux to share with them our bacterial cellulose.
August 29th, 2018: First work group with Le Catalyseur
Le Catalyseur is a business incubator, they helped us to write our business plan. This first work group allowed us to structure our company.
August 31st, 2018: Second workshop with Le Catalyseur
During this second meeting, we have worked on the different risk factors to enhance our business.
NOTEBOOK: SEPTEMBER
September 4th, 2018
Le Catalyseur helps us to create a business CANVAS.
September 5th, 2018:
Le Catalyseur helps us to define our strengths, weakness as a business.
NOTEBOOK: OCTOBER
October 3rd, 2018:
We do a general repetition in an international high school near Toulouse.
October 5th, 2018:
Another meeting with Le Catalyseur to talk about industrial property.
No dogs were harmed over the course of this iGEM project.
The whole Toulouse INSA-UPS team wants to thank our sponsors, especially:
And many more. For futher information about our sponsors, please consult our Sponsors page.
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