Difference between revisions of "Team:Toulouse France/Collaborations"

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<div id="pageintro" class="hoc clear" style="padding:300px 0px;">  
 
<div id="pageintro" class="hoc clear" style="padding:300px 0px;">  
<center><p class="sec_title_trans">Collaborations and Meet Up</p></center>
+
<center><p class="sec_title_trans">Collaborations and Meet Ups</p></center>
 
 
 
</div>
 
</div>
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<p class="texteb">
 
<p class="texteb">
 
Our team decided to create protocol videos in order to help young scientists to manipulate.  
 
Our team decided to create protocol videos in order to help young scientists to manipulate.  
When people are working on <b>Genetics engineering</b>, there are several <b>basic experiments</b> that have to be controlled.  
+
When people are working on <b>Genetic engineering</b>, there are several <b>basic experiments</b> that have to be mastered.  
 
During our experiments, we filmed 4 steps of cloning: <b>PCR</b>, <b>digestion</b>, <b>ligation</b> and <b>transformation</b>.  
 
During our experiments, we filmed 4 steps of cloning: <b>PCR</b>, <b>digestion</b>, <b>ligation</b> and <b>transformation</b>.  
<br>Watching it, people could see how to manipulate safely.  
+
<br>By watching it, people will see how to manipulate safely.  
We asked other igem teams to translate protocols in their mother tongue.  
+
We asked other igem teams to translate the protocols in their mother tongue.  
We obtained protocol videos in <b>English</b> with <b><a href="https://2016.igem.org/Team:Imperial_College">Imperial College</a></b> team,  
+
We obtained protocol videos in <b>English</b> with the <b><a href="https://2016.igem.org/Team:Imperial_College">Imperial College</a></b> team,  
 
in <b>Spanish</b> thanks to the <b><a href="https://2016.igem.org/Team:Tec-Monterrey">TEC-Monterrey</a></b> team,  
 
in <b>Spanish</b> thanks to the <b><a href="https://2016.igem.org/Team:Tec-Monterrey">TEC-Monterrey</a></b> team,  
in <b>Dutch</b> with <b><a href="https://2016.igem.org/Team:Leiden">Leiden</a></b> team,  
+
in <b>Dutch</b> with the <b><a href="https://2016.igem.org/Team:Leiden">Leiden</a></b> team,  
in <b>Chinese</b> with <b><a href="https://2016.igem.org/Team:BIT">BIT</a></b> team,  
+
in <b>Chinese</b> with the <b><a href="https://2016.igem.org/Team:BIT">BIT</a></b> team,  
in <b>Portuguese</b> thanks to <b><a href="https://2016.igem.org/Team:USP-EEL-Brazil">EEL</a></b> team,  
+
in <b>Portuguese</b> thanks to the <b><a href="https://2016.igem.org/Team:USP-EEL-Brazil">EEL</a></b> team,  
in <b>German</b> with <b><a href="https://2016.igem.org/Team:Hamburg">Hamburg</a></b> team and  
+
in <b>German</b> with the <b><a href="https://2016.igem.org/Team:Hamburg">Hamburg</a></b> team and  
 
in <b>French</b> with the collaboration of the <b><a href="https://2016.igem.org/Team:Bordeaux">Bordeaux</a></b> team. 
 
in <b>French</b> with the collaboration of the <b><a href="https://2016.igem.org/Team:Bordeaux">Bordeaux</a></b> team. 
We wrote the entire script and we added some <b>guidance</b> in red (minutes for each paragraphs for instance). Teams had to translate and record the script.
+
We wrote the entire script in English and we added some <b>guidance</b> in red (minutes for each paragraphs for instance). Teams had to translate and record the script.
Now, we possess a lot of protocols explained in <b>six</b> different languages, accessible to everybody on <b>Youtube</b> and on our wiki.  
+
Now, we possess the four protocols explained in <b>six</b> different languages, accessible to everybody on <b>Youtube</b> and on our wiki.  
 
</p>
 
</p>
 
</div>
 
</div>
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<div id="teamGallery2">
 
<div id="teamGallery2">
 
<h2>Digestion</h2>
 
<h2>Digestion</h2>
<p>This video presents the protocol to do enzymatic digestion of a DNA sample. This technique is useful for usual clonings. </p>
+
<p>This video presents the protocol to do enzymatic digestion of a DNA sample. This technique is useful for usual clonings but it also have larger applications in genetics because it is used to characterize DNA. </p>
  
 
<div class="box">
 
<div class="box">
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<div id="teamGallery2">
 
<div id="teamGallery2">
 
<h2>Ligation</h2>
 
<h2>Ligation</h2>
<p>When a DNA fragment is digested with digestion enzymes, it is possible to ligate its extremities with another digested fragment, if the extremities are cohesives. This method can be used to add an insert in a vector or a backbone. </p>
+
<p>When a DNA fragment is digested with restriction enzymes, it is possible to ligate its extremities with another digested fragment, if the extremities are cohesives. This method can be used to add an insert in a vector or a backbone. </p>
  
 
 
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<div id="teamGallery2">
 
<div id="teamGallery2">
 
<h2>PCR</h2>
 
<h2>PCR</h2>
<p>PCR, or Polymerase Chain Reaction, is a technique that amplify a DNA sequence by using primers and DNA polymerase. Throughout this video, you will see how to perform a PCR. A theoretical explanation of the way how PCR works ends the video. </p>
+
<p>PCR, or Polymerase Chain Reaction, is a technique that amplifies a DNA sequence by using primers and DNA polymerase. Throughout this video, you will see how to perform a PCR. A theoretical explanation of why PCR is possible ends the video. </p>
 
 
 
 
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<div id="teamGallery2">
 
<div id="teamGallery2">
 
<h2>Transformation</h2>
 
<h2>Transformation</h2>
<p>A transformation is a method that allows to insert a plasmid in a <i> E. coli</i> bacteria. Several method to transform a bacteria exist, but we chose to use a thermal shock method for bacteria to become permeable. </p>
+
<p>Transformation is a method that allows inserting DNA in bacteria. Several methods to transform bacteria exist, but we chose to explain a thermal shock method in <i>E. coli</i>. </p>
  
 
<div class="box">
 
<div class="box">
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<p class="texteb">
 
<p class="texteb">
 
<center><img src="https://static.igem.org/mediawiki/2016/3/3e/Toulouse_France_erlenmeyers.jpg" style="margin-top:20px;"></center>
 
<center><img src="https://static.igem.org/mediawiki/2016/3/3e/Toulouse_France_erlenmeyers.jpg" style="margin-top:20px;"></center>
<br><br>In exchange for recording the script in English, we studied the optimal growth of Bacillus subtilis and Pseudomonas fluorescens for the <a href="https://2016.igem.org/Team:Imperial_College">Imperial London College team</a>. First, we did an experimental plan to observe if pH is in interaction with temperature. Finally, the conclusion was that pH and temperature were two independent parameters. We ran the experiments again, changing only one parameter.
+
<br><br>In exchange for recording the script in English, we studied the optimal growth of <i>Bacillus subtilis</i> and <i>Pseudomonas fluorescens</i> for the <a href="https://2016.igem.org/Team:Imperial_College">Imperial London College team</a>. First, we did an experimental plan to observe if pH is in interaction with temperature. Finally, the conclusion was that pH and temperature are two independent parameters. So, we ran the experiments again, changing only one of the parameters.
 
</p>
 
</p>
 
<br><br>
 
<br><br>
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<u><p class="title1" id="select1" style="text-align:center">3D conception</p></u>
 
<u><p class="title1" id="select1" style="text-align:center">3D conception</p></u>
 
<p class="texteb">
 
<p class="texteb">
+
As we added 3D conception to our set of skills, the Bordeaux team asked us to do 3D conceptions and animate them using the Blender software. We gave us short videos to put on their wiki.
We did a 3D Conception of the iGEM Bordeaux Team, on Blender.
+
We did a 3D Conception of their logo.
 
<center><img src="" style="width:100%"></center>
 
<center><img src="" style="width:100%"></center>
 
 
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<p class="texteb">
 
<p class="texteb">
  
We want to thank <a href="https://2016.igem.org/Team:Aix-Marseille">Aix-Marseille team</a> for the great help they give to us.  
+
We want to thank <a href="https://2016.igem.org/Team:Aix-Marseille">Aix-Marseille team</a> for the great help they gave to us.  
 
The aim of the model they conceived for us is to assess the evolution of plasmids throughout the culture,  
 
The aim of the model they conceived for us is to assess the evolution of plasmids throughout the culture,  
 
to determine which parameters can matter in the loss of those plasmids,  
 
to determine which parameters can matter in the loss of those plasmids,  
and to precise what are the probabilities for a bacteria to loose its plasmids during cell division.  
+
and to precise what are the probabilities for a bacterium to loose its plasmids during cell division.  
As a plasmids can be a disadvantage for growth (energy spent into replicating processes) or a advantage  
+
As a plasmids can be a disadvantage for growth (because of the energy spent into replicating processes) or an advantage  
(protection against a toxin) this question is hard to answer.  
+
(protection against a toxin for example) this question is hard to answer to.  
But in this situation, where one type of plasmid can influence on the presence of the other type of plasmid in (and reciprocally)  
+
But in this situation, where one type of plasmid can influence on the presence of the other one present (and reciprocally)  
in the same bacteria, the question become too tough to answer and only a mathematical model can resolve such a interrogation!  
+
in the same bacteria, the answer is really tough to get and only a mathematical model can resolve such a interrogation!  
  
 
<center>
 
<center>
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<u><p class="title1" id="select1" style="text-align:center">Receipt of plasmids</p></u>
 
<u><p class="title1" id="select1" style="text-align:center">Receipt of plasmids</p></u>
 
<p class="texteb">
 
<p class="texteb">
We want to thank the 2012 <a href="https://2012.igem.org/Team:LMU-Munich">Munich team</a> for sending us 4 different shuttle plasmids. One of these, pBs0k-p, was very useful because we used it for cloning in E.coli and Bacillus subtilis.
+
We want to thank the 2012 <a href="https://2012.igem.org/Team:LMU-Munich">Munich team</a> for sending us 4 different shuttle plasmids. One of these, pSBBS0K-P, was very useful because we used it for cloning in <i>E.coli</i> and <i>Bacillus subtilis</i>.
 
</p>
 
</p>
 
<center><img src="" style="width:15%"></center>
 
<center><img src="" style="width:15%"></center>
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<u><p class="title1" id="select1" style="text-align:center">Mailing of kit</p></u>
 
<u><p class="title1" id="select1" style="text-align:center">Mailing of kit</p></u>
 
<p class="texteb">
 
<p class="texteb">
2016 <a href="https://2016.igem.org/Team:Evry">Evry team</a> asked us to send a Ludox solution that was in our iGEM Kit. They stored their own solution at -20°C so it was not usable anymore. But it was important for them to participate to the InterLab project so we helped them.
+
The 2016 <a href="https://2016.igem.org/Team:Evry">Evry team</a> asked us to send a Ludox solution that was in our iGEM Kit. They stored their own solution at -20°C so it was not usable anymore. But it was important for them to participate to the InterLab project so we helped them.
 
</p>
 
</p>
 
<center><img src="https://static.igem.org/mediawiki/2016/8/88/Toulouse_France_logoevry.jpg" style="width:15%"></center>
 
<center><img src="https://static.igem.org/mediawiki/2016/8/88/Toulouse_France_logoevry.jpg" style="width:15%"></center>
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<u><p class="title1" id="select1" style="text-align:center">Protocol translation</p></u>
 
<u><p class="title1" id="select1" style="text-align:center">Protocol translation</p></u>
 
<p class="texteb">
 
<p class="texteb">
2016 <a href="https://2016.igem.org/Team:METU_HS_Ankara">METU HS Ankara</a> team wanted to create a database, which consists of different language protocols. They asked us to translate their protocol in French.
+
2016 <a href="https://2016.igem.org/Team:METU_HS_Ankara">METU HS Ankara</a> team wanted to create a database, which consists of different language protocols. They asked us to translate their protocols in French.
 
</p>
 
</p>
 
 
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more about other brilliant projects. We met a lot of nice people from different teams and
 
more about other brilliant projects. We met a lot of nice people from different teams and
  
we sympathized a lot with every French team.
+
we sympathized a lot with every French teams.
  
 
<br>
 
<br>
 
<br>
 
<br>
The organizers arranged two lectures during the weekend. First it dealt with the challenges
+
The organizers arranged two lectures during the weekend. The first one dealt with the challenges
  
 
and the risks of synthetic biology and the second talked about a new economic world.
 
and the risks of synthetic biology and the second talked about a new economic world.
Line 1,008: Line 1,008:
 
animated these round tables. One of our best memories was to meet the founder of iGEM:
 
animated these round tables. One of our best memories was to meet the founder of iGEM:
  
<b>Randy Rettberg</b>. It was an honor for us to speak with this person and to explain our project.
+
<b>Randy Rettberg</b>. It was an honor for us to speak with him and to explain our project.
  
 
<br>
 
<br>
Line 1,044: Line 1,044:
 
One day, on our Facebook page, we received a message from Itzel Guzman, iGEM TEC
 
One day, on our Facebook page, we received a message from Itzel Guzman, iGEM TEC
  
Monterrey team member. She was in Toulouse for a semester and she asked us to meet us,
+
Monterrey team member. She was in Toulouse for a few months and she asked us to meet us,
  
the iGEM Toulouse team. We discussed a long time on our project over a drink and we
+
the iGEM Toulouse team. We discussed a long time about our respective projects over a drink and we
  
 
sympathized a lot!
 
sympathized a lot!

Revision as of 11:14, 19 October 2016

iGEM Toulouse 2016

Collaborations and Meet Ups


Our Collaborations

Protocol videos

Our team decided to create protocol videos in order to help young scientists to manipulate. When people are working on Genetic engineering, there are several basic experiments that have to be mastered. During our experiments, we filmed 4 steps of cloning: PCR, digestion, ligation and transformation.
By watching it, people will see how to manipulate safely. We asked other igem teams to translate the protocols in their mother tongue. We obtained protocol videos in English with the Imperial College team, in Spanish thanks to the TEC-Monterrey team, in Dutch with the Leiden team, in Chinese with the BIT team, in Portuguese thanks to the EEL team, in German with the Hamburg team and in French with the collaboration of the Bordeaux team.  We wrote the entire script in English and we added some guidance in red (minutes for each paragraphs for instance). Teams had to translate and record the script. Now, we possess the four protocols explained in six different languages, accessible to everybody on Youtube and on our wiki.

Digestion

This video presents the protocol to do enzymatic digestion of a DNA sample. This technique is useful for usual clonings but it also have larger applications in genetics because it is used to characterize DNA.



Imperial College of London team



Leiden Team



EEL Brazil Team



Tec-Monterrey Team



Bordeaux Team



BIT Team



LMU & TU Munich Team

Ligation

When a DNA fragment is digested with restriction enzymes, it is possible to ligate its extremities with another digested fragment, if the extremities are cohesives. This method can be used to add an insert in a vector or a backbone.



Imperial College of London team



Leiden Team



EEL Brazil Team



Tec-Monterrey Team



Bordeaux Team



BIT Team



LMU & TU Munich Team

PCR

PCR, or Polymerase Chain Reaction, is a technique that amplifies a DNA sequence by using primers and DNA polymerase. Throughout this video, you will see how to perform a PCR. A theoretical explanation of why PCR is possible ends the video.



Imperial College of London team



Leiden Team



EEL Brazil Team



Tec-Monterrey Team



Bordeaux Team



BIT Team



LMU & TU Munich Team

Transformation

Transformation is a method that allows inserting DNA in bacteria. Several methods to transform bacteria exist, but we chose to explain a thermal shock method in E. coli.



Imperial College of London team



Leiden Team



EEL Brazil Team



Tec-Monterrey Team



BIT Team



Bordeaux Team



LMU & TU Munich Team





Growth study of B. subtilis and P. fluorescens



In exchange for recording the script in English, we studied the optimal growth of Bacillus subtilis and Pseudomonas fluorescens for the Imperial London College team. First, we did an experimental plan to observe if pH is in interaction with temperature. Finally, the conclusion was that pH and temperature are two independent parameters. So, we ran the experiments again, changing only one of the parameters.



Results

Optimum Temperature (°C)

Optimum pH

Doubling time (minutes)

Bacillus subtilis (WT 168)

34-37

8

41

Pseudomonas fluorescens (SBW25)

<29

7,5

<80



Optimum temperatures and pH and the doubling times are summarized in the table for our two strains.

3D conception

As we added 3D conception to our set of skills, the Bordeaux team asked us to do 3D conceptions and animate them using the Blender software. We gave us short videos to put on their wiki. We did a 3D Conception of their logo.

We also did a 3D conception of their laboratory benching.

Model of the plasmid loss

We want to thank Aix-Marseille team for the great help they gave to us. The aim of the model they conceived for us is to assess the evolution of plasmids throughout the culture, to determine which parameters can matter in the loss of those plasmids, and to precise what are the probabilities for a bacterium to loose its plasmids during cell division. As a plasmids can be a disadvantage for growth (because of the energy spent into replicating processes) or an advantage (protection against a toxin for example) this question is hard to answer to. But in this situation, where one type of plasmid can influence on the presence of the other one present (and reciprocally) in the same bacteria, the answer is really tough to get and only a mathematical model can resolve such a interrogation!

Click here to see the model they developped

Receipt of plasmids

We want to thank the 2012 Munich team for sending us 4 different shuttle plasmids. One of these, pSBBS0K-P, was very useful because we used it for cloning in E.coli and Bacillus subtilis.

Mailing of kit

The 2016 Evry team asked us to send a Ludox solution that was in our iGEM Kit. They stored their own solution at -20°C so it was not usable anymore. But it was important for them to participate to the InterLab project so we helped them.

Protocol translation

2016 METU HS Ankara team wanted to create a database, which consists of different language protocols. They asked us to translate their protocols in French.

Surveys

We filled in different surveys all along the year. Among them, surveys for:





Meet Ups





The European Experience

The Evry and Ionis teams organized on the 1st and 2nd of July, a huge meeting that gathered more than 11 European teams. In different rooms, each team had a space to hang its poster and set up flyers and communication supports. We explained our project and discussed with other iGEM members. Some helped us on different aspects like modeling and confinement of our bacteria. When we were not on our stand, we walked around the rooms and learnt more about other brilliant projects. We met a lot of nice people from different teams and we sympathized a lot with every French teams.

The organizers arranged two lectures during the weekend. The first one dealt with the challenges and the risks of synthetic biology and the second talked about a new economic world. Different people, like CEOs of company, trainees, young workers, or research scientists animated these round tables. One of our best memories was to meet the founder of iGEM: Randy Rettberg. It was an honor for us to speak with him and to explain our project.

We thank very much the organizing teams for these amazing days in Paris! It was for us an enjoyable experience of what the Giant Jamboree will be in October.


Meeting with Itzel from TEC Monterrey team

One day, on our Facebook page, we received a message from Itzel Guzman, iGEM TEC Monterrey team member. She was in Toulouse for a few months and she asked us to meet us, the iGEM Toulouse team. We discussed a long time about our respective projects over a drink and we sympathized a lot! We decided to collaborate together on the protocol videos (view more).






Contacts