Difference between revisions of "Team:Toulouse-INSA-UPS/Notebook"
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| − | <p> Here, you will find information about the | + | <p> Here, you will find information about the timeline of our project.</p> |
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<h2 class="heavy">LABBOOK</h2> | <h2 class="heavy">LABBOOK</h2> | ||
<hr/> | <hr/> | ||
| − | <p>To achieve our lab work, we | + | <p>To achieve our lab work, we split up into different teams, each working on different aspects of the experimental procedure. Three teams were then formed :</p> |
<ul> | <ul> | ||
<li><strong>Team coli</strong>: this team was managed by <strong>Younes</strong> and included <strong>Marion</strong>. Their goal was to achieve the production and characterization of Cerberus and Sirius in <em>Escherichia coli</em></li> | <li><strong>Team coli</strong>: this team was managed by <strong>Younes</strong> and included <strong>Marion</strong>. Their goal was to achieve the production and characterization of Cerberus and Sirius in <em>Escherichia coli</em></li> | ||
<li><strong>Team pastoris</strong>: this team was ruled by <strong>Angeline</strong> and included <strong>Gaëlle</strong>. Their mission was to reproduce the experiments planned on <em>Escherichia coli</em> in <em>Pichia pastoris</em> </li> | <li><strong>Team pastoris</strong>: this team was ruled by <strong>Angeline</strong> and included <strong>Gaëlle</strong>. Their mission was to reproduce the experiments planned on <em>Escherichia coli</em> in <em>Pichia pastoris</em> </li> | ||
<li><strong>Team biotin</strong>: this team was ruled by <strong>Amandine</strong> and included <strong>Jean</strong> and <strong>Julien</strong>. Their objective was to construct and to test our <em>in vivo</em> biotinylation system.</li> | <li><strong>Team biotin</strong>: this team was ruled by <strong>Amandine</strong> and included <strong>Jean</strong> and <strong>Julien</strong>. Their objective was to construct and to test our <em>in vivo</em> biotinylation system.</li> | ||
| − | <li><strong>Team callulose</strong>: this team was managed by <strong>Callum</strong> (so | + | <li><strong>Team callulose</strong>: this team was managed by <strong>Callum</strong> (and so was dubbed Callulose) and got help from <strong>Younes</strong>. Its mission was to launch and optimize our bacterial cellulose production. </li> |
</ul> | </ul> | ||
</div> | </div> | ||
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<h4 class="heavy">18/06 - 22/06:</h4> | <h4 class="heavy">18/06 - 22/06:</h4> | ||
<p> | <p> | ||
| − | For the first week in the lab, we | + | For the first week in the lab, we received and amplified our plasmids (pPICz, pETDuet, pET28, pGAP) but also our bacterial strains <i>E. coli</i> BL21 DE3 and Tuner. |
</p> | </p> | ||
| Line 115: | Line 115: | ||
<h4 class="heavy">25/06 - 29/06:</h4> | <h4 class="heavy">25/06 - 29/06:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team coli</strong>: we started with a PCR on the the | + | <li><strong>Team coli</strong>: we started with a PCR on the the gBlock Cerberus-pastoris. In order to clone this gBlock, we prepared the pGAP plasmid by amplifying it in <i>E. coli</i> Stellar cells before a Midiprep. Another aspect was to check the pREAV which will allow the incorporation of a unnatural amino acid in our Cerberus.</li> |
| − | <li><strong>Team pastoris</strong>: pPIC, pGAP and pETDuet were good but pPIC did not | + | <li><strong>Team pastoris</strong>: pPIC, pGAP and pETDuet were good but pPIC did not match our expectations so we had to find another solution.</li> |
<li><strong>Team callulose</strong>: the first productions of cellulose started in culture tubes.</li> | <li><strong>Team callulose</strong>: the first productions of cellulose started in culture tubes.</li> | ||
| Line 147: | Line 147: | ||
<h4 class="heavy">02/07 - 06/07:</h4> | <h4 class="heavy">02/07 - 06/07:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team biotin</strong>: this week, we | + | <li><strong>Team biotin</strong>: this week, we performed a PCR on BirA and we digested the pPIC after its amplification in <i>E. coli</i> Stellar cells. This allowed us to do our first cloning with BirA in the pETDuet. We checked the clones by digestion and they were OK. It was necessary to sequence these clones before doing the next cloning in pETDuet. We obtained a different pPIC from a previous year's supplies, and we checked it. |
</li> | </li> | ||
| − | <li><strong>Team coli</strong>: 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 | + | <li><strong>Team coli</strong>: 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 constructs by digestion before sending them for sequencing. In the same time we checked our plasmid pEVOL-AzF which allows the unnatural amino acid incorporation in <i>E. coli</i>. |
</li> | </li> | ||
| − | <li><strong>Team pastoris</strong>: this week, we | + | <li><strong>Team pastoris</strong>: this week, we clone Cerberus-streptavidin though In-fusion into the 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 <i>Pichia pastoris</i> GS200 strains cell. |
</li> | </li> | ||
</ul> | </ul> | ||
| Line 170: | Line 170: | ||
<ul> | <ul> | ||
| − | <li><strong>Team biotin:</strong> 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 | + | <li><strong>Team biotin:</strong> 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 PCRs with the parts that will be used to functionalize our Cerberus after biotinylation by BirA. </li> |
| − | <li><strong>Team coli:</strong> This week, we received the sequencing results for Cerberus and it was again a | + | <li><strong>Team coli:</strong> This week, we received the sequencing results for Cerberus and it was again a success for the Toulouse iGEM team. We cloned Sirius (CBM3-RFP) in the pET28 with the In-fusion kit. For this, we performed PCR on the gBlocks then we used the In-fusion kit. After verification, Sirius was OK. |
</li> | </li> | ||
| − | <li><strong>Team pastoris:</strong> we checked the pREAV and found out the plasmid map didn’t | + | <li><strong>Team pastoris:</strong> we checked the pREAV and found out the plasmid map didn’t match with our digestion results. We needed to find a different pREAV... </li> |
| − | <li><strong>Team callulose:</strong> we decided to focus the production with <i>G. hansenii</i> because it produces more cellulose than <i>K. rhaeticus</i>. We also started | + | <li><strong>Team callulose:</strong> we decided to focus the production with <i>G. hansenii</i> because it produces more cellulose than <i>K. rhaeticus</i>. We also started production in 2L Erlenmeyers. </li> |
</ul> | </ul> | ||
| Line 193: | Line 193: | ||
<h4 class="heavy">16/07 - 20/07:</h4> | <h4 class="heavy">16/07 - 20/07:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team biotin:</strong> This week, we focused on the pastoris cloning. | + | <li><strong>Team biotin:</strong> This week, we focused on the pastoris cloning. We prepared the pGAP vector (amplification, purification and digestion), mRFP1, BFP and scygonadin parts and we cloned all three. We tried to amplify and purify pPIC but unfortunately it was necessary to try again because the Midiprep didn’t succeed.</li> |
<li><strong>Team coli:</strong> this week, we made or own competent cells using BL21 DE3 and tuner strains</li> | <li><strong>Team coli:</strong> this week, we made or own competent cells using BL21 DE3 and tuner strains</li> | ||
<li><strong>Team pastoris:</strong> 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.</li> | <li><strong>Team pastoris:</strong> 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.</li> | ||
| Line 212: | Line 212: | ||
<h4 class="heavy">23/07 - 27/07:</h4> | <h4 class="heavy">23/07 - 27/07:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team biotin:</strong> this week, before another midiprep, we checked the pPIC but we still had a mapping problem. After many | + | <li><strong>Team biotin:</strong> this week, before another midiprep, we checked the pPIC but we still had a mapping problem. After many verifications, it was clearly not correct but we found another source for this plasmid and it seemed OK. We amplified it by midiprep.</li> |
<li><strong>Team coli:</strong> this week, we did the first production assay for Sirius and we were very happy because we obtained a red culture medium.</li> | <li><strong>Team coli:</strong> this week, we did the first production assay for Sirius and we were very happy because we obtained a red culture medium.</li> | ||
<li><strong>Team pastoris:</strong> this week, the pichia team helped the other teams because it was ahead of the planning and had to wait for yeast growth.</li> | <li><strong>Team pastoris:</strong> this week, the pichia team helped the other teams because it was ahead of the planning and had to wait for yeast growth.</li> | ||
| Line 232: | Line 232: | ||
<h4 class="heavy">30/07 - 03/08:</h4> | <h4 class="heavy">30/07 - 03/08:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team biotin:</strong> this week, we worked on pETDuet-BirA to clone our | + | <li><strong>Team biotin:</strong> this week, we worked on pETDuet-BirA to clone our functionalizing 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 <i>E. coli</i> BL21 DE3.</li> |
| − | <li><strong>Team coli:</strong> we did the first Sirius purification after production in <i>E. coli</i> BL21 DE3. To do this, we used an IMAC column and dialysis. In order to | + | <li><strong>Team coli:</strong> we did the first Sirius purification after production in <i>E. coli</i> BL21 DE3. To do this, we used an IMAC column and dialysis. In order to prove the CBM3 fixation to cellulose, we prepared the regenerated amorphous cellulose.</li> |
<li><strong>Team callulose:</strong> We intensified the cellulose production to be able to give 5g of dried cellulose to the Bordeaux iGEM team at the end of the month.</li> | <li><strong>Team callulose:</strong> We intensified the cellulose production to be able to give 5g of dried cellulose to the Bordeaux iGEM team at the end of the month.</li> | ||
| Line 305: | Line 305: | ||
<h4 class="heavy">20/08 - 24/08:</h4> | <h4 class="heavy">20/08 - 24/08:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team coli:</strong> this week was a particularly busy week. We | + | <li><strong>Team coli:</strong> this week was a particularly busy week. We produced and purified Orthos as well as 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 produced Cerberus. To do this, we co-transformed BL21 DE3 cells with pET28 Cerberus and pEVOL AzF. The cell culture medium was complemented with the AzF unnatural amino acid to allow its incorporation. Cerberus was purified by a cellulose pull-down assay.</li> |
| − | <li><strong>Team pSB1C3:</strong> we created this new team to start the pSB1C3 clonings. | + | <li><strong>Team pSB1C3:</strong> we created this new team to start the pSB1C3 clonings. PCRs were performed on our gBlocks. Unfortunately, we didn’t manage to amplify all the gBlocks.</li> |
</ul> | </ul> | ||
</div> | </div> | ||
| Line 358: | Line 358: | ||
<h4 class="heavy">03/09 - 07/09:</h4> | <h4 class="heavy">03/09 - 07/09:</h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team coli:</strong> in order to demonstrate the efficiency of the AzF head, we tried to click paramagnetic beads on it. The aim was to see the | + | <li><strong>Team coli:</strong> in order to demonstrate the efficiency of the AzF head, we tried to click paramagnetic beads on it. The aim was to see the movement of cellulose in a presence of a magnet</li> |
| − | <li><strong>Team pSB1C3:</strong> this week, we tried | + | <li><strong>Team pSB1C3:</strong> this week, we tried the pSB1C3 clonings again. 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 for sequencing. </li> |
</ul> | </ul> | ||
| Line 376: | Line 376: | ||
<h4 class="heavy">10/09 - 14/09: </h4> | <h4 class="heavy">10/09 - 14/09: </h4> | ||
<ul> | <ul> | ||
| − | <li><strong>Team biotin:</strong> we successfully | + | <li><strong>Team biotin:</strong> we successfully pulled Orthos down to measure the BFP fluorescence with and without Orthos on cellulose.</li> |
</ul> | </ul> | ||
Revision as of 01:20, 17 October 2018
NOTEBOOK
Here, you will find information about the timeline of our project.
LABBOOK
To achieve our lab work, we split up 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 pastoris: 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 Callum (and so was dubbed Callulose) 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 received and amplified 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 gBlock Cerberus-pastoris. In order to clone this gBlock, we prepared the pGAP plasmid by amplifying it in E. coli Stellar 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 pastoris: pPIC, pGAP and pETDuet were good but pPIC did not match our expectations so we had to find another solution.
- Team callulose: the first productions of cellulose started in culture tubes.
LABBOOK: JULY
02/07 - 06/07:
- Team biotin: this week, we performed a PCR on BirA and we digested the pPIC after its amplification in E. coli Stellar cells. This allowed us to do our first cloning with BirA in the pETDuet. We checked the clones by digestion and they were OK. It was necessary to sequence these clones before doing the next cloning in pETDuet. We obtained a different pPIC from a previous year's supplies, 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 constructs by digestion before sending them for sequencing. In the same time we checked our plasmid pEVOL-AzF which allows the unnatural amino acid incorporation in E. coli.
- Team pastoris: this week, we clone Cerberus-streptavidin though In-fusion into the 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 Pichia pastoris 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 PCRs with the parts that will be used to functionalize our Cerberus after biotinylation by BirA.
- Team coli: This week, we received the sequencing results for Cerberus and it was again a success for the Toulouse iGEM team. We cloned Sirius (CBM3-RFP) in the pET28 with the In-fusion kit. For this, we performed PCR on the gBlocks then we used the In-fusion kit. After verification, Sirius was OK.
- Team pastoris: we checked the pREAV and found out the plasmid map didn’t match with our digestion results. We needed to find a different pREAV...
- Team callulose: we decided to focus the production with G. hansenii because it produces more cellulose than K. rhaeticus. We also started production in 2L Erlenmeyers.
16/07 - 20/07:
- Team biotin: This week, we focused on the pastoris cloning. We prepared the pGAP vector (amplification, purification and digestion), mRFP1, BFP and scygonadin parts and we cloned all three. We tried to amplify and purify pPIC but unfortunately it was necessary to try again because the Midiprep didn’t succeed.
- Team coli: this week, we made or own competent cells using BL21 DE3 and tuner strains
- Team pastoris: 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 verifications, it was clearly not correct 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 pastoris: 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 functionalizing 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 DE3.
- Team coli: we did the first Sirius purification after production in E. coli BL21 DE3. To do this, we used an IMAC column and dialysis. In order to prove the CBM3 fixation to cellulose, we prepared the regenerated amorphous cellulose.
- Team callulose: We intensified the cellulose production to be able to give 5g of dried cellulose to the Bordeaux iGEM team at the end of the month.
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, scygonadin 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 produced and purified Orthos as well as 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 produced Cerberus. To do this, we co-transformed BL21 DE3 cells with pET28 Cerberus and pEVOL AzF. The cell culture medium was complemented with the AzF unnatural amino acid to allow its incorporation. Cerberus was purified by a cellulose pull-down assay.
- Team pSB1C3: we created this new team to start the pSB1C3 clonings. PCRs were performed on our gBlocks. Unfortunately, we didn’t manage 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 DBCO-fluorescein.
LABBOOK: SEPTEMBER
03/09 - 07/09:
- Team coli: in order to demonstrate the efficiency of the AzF head, we tried to click paramagnetic beads on it. The aim was to see the movement of cellulose in a presence of a magnet
- Team pSB1C3: this week, we tried the pSB1C3 clonings again. 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 for sequencing.
10/09 - 14/09:
- Team biotin: we successfully pulled Orthos down 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 & callulose: for our last lab week, we managed to produce a pink bacterial cellulose by using our purified Sirius protein.
Extra-LabBook
Here, you can find about some of our activities outside of the lab. More details are provided in the HP LogBook of the Integrated Human Practices section.
Extra-LabBOOK: FEBRUARY
February 1st, 2018: Kick-off meeting
First meeting of the team, distribution of the tasks and of course we got to know each other.
The iGEM’s adventure began!
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 needed more investigations.
February 21st, 2018: Escape game conference
We attended a conference organized by Le Catalyseur on the creation of a teaching escape game. We met two professors in high schools option “Sciences and Technologies of the Laboratory” (STL).
Extra-LabBOOK: 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 met a CRISPR/CAS expert in the LMGM lab who taught us a lot about the new possibilities of the system.
Extra-LabBOOK: APRIL
April 5th, 2018: Final choice of our project
After a long period of brainstorming, we decided to work on the binding of molecules on cellulose. Then, we had to think about the name of our project.
April 12th, 2018: Tour des Sciences
We presented the Microbioworld game during the ”Tour des sciences”.
Extra-LabBOOK: MAY
May , 2018:
We worked on the design of the project with the help of our supervisors.
May 31th, 2018:
We met Philippe Serp and his team to talk about experimenting in his lab. We needed them to activate our graphene before using it to functionalise cellulose.
Extra-LabBOOK: JUNE
June 18th, 2018: First day in the lab
We were all very impatient, and finally it has come! It’s the first lab day.
June 19th, 2018: Foundation INSA Toulouse meeting
Looking for funds, we presented our project to the INSA Toulouse foundation.
June 23rd-24th, 2018: Collaboration with the Montpellier iGEM team
We started a collaboration with the Montpellier team to help them in some areas like the wiki. To do so, we went to Montpellier to talk with them and share our knowledge of the competition.
June 25th, 2018: TWB meeting
We met Pierre Monsan, one of the main founders of one of our sponsors, Toulouse White Biotechnology (TWB).
June 26th, 2018: NUS meeting
We organized a Skype meeting with the NUS iGEM team to discuss about a possible collaboration.
June 27th, 2018: Meet with STL teachers
As part of our discussions with the french ministry of education, high school teachers visited the lab where we worked during summer.
June 27th, 2018
For our entrepreneurship approach, we met Guillaume Boissonat who co-funded the startup pili.bio. He shared with us his own experience as a co-funder, and he gave us some advice about the possible business model for a Cerberus startup.
June 29th, 2018: Primary school intervention
We intervened in a primary school in order to present Microbiolworld, the research profession, and more generally to introduce the world of microbes to children.
Extra-LabBOOK: JULY
July 5th, 2018: CALMIP’s meet and visit
We visited CALMIP, a high-throughput calcul center which allowed us to make complex calculations for our modelling.
July 6th, 2018: Official announcement of our project
We officially announced the purpose of our project on social medias!
July 7th, 2018: 4th Annual parisian meet-up
We took part in the annual parisian meet-up organized by the 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 to the public.
July 19th, 2018: First publications in french newspapers/h4>
Newspapers from Toulouse interviewed us about our Cerberus project, we were very happy and grateful for this recognition!
July 20th-22nd, 2018: European meet-up in Munich
Two members of the team travelled to Munich to represent our team at the European meet-up.
July 30th, 2018: Incubator meeting
We met Yohann Bouvier who is the manager of a startup incubator, named "le starter". He gave us some advice regarding our entrepreneurship approach.
Extra-LabBOOK: AUGUST
August 1st, 2018: Laval skype
We contacted the Laval iGEM team in order to create an innovative human practices collaboration.
August 17th, 2018: Shooting photo for the wiki
We dressed up to take the photos for our wiki.
August 25th-26th, 2018: Collaboration with Bordeaux iGEM team
We went to Bordeaux to bring them our bacterial cellulose, so they could use it as another carbon source for there Far Waste project.
August 29th, 2018: First working group with Le Catalyseur
Le Catalyseur is a business incubator, they helped us to write our business plan. This first session allowed us to structure our company and defined our objectives.
August 31st, 2018: Second workshop with Le Catalyseur
During this second meeting, we identified the critical points and risk factors we needed to enhance to conduct Cerberus as a business.
Extra-LabBOOK: SEPTEMBER
September 4th, 2018
Le Catalyseur helped us to create a business model CANVAS.
September 5th, 2018:
Le Catalyseur helped us to create a SWOT matrice to define our strengths and weaknesses as a business.
Extra-LabBOOK: OCTOBER
October 3rd, 2018:
We have done 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.
The content provided on this website is the fruit of the work of the Toulouse INSA-UPS iGEM Team. As a deliverable for the iGEM Competition, it falls under the Creative Commons Attribution 4.0. Thus, all content on this wiki is available under the Creative Commons Attribution 4.0 license (or any later version). For futher information, please consult the official website of Creative Commons.
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