"
Team:Paris Bettencourt/Experiments/List
From 2011.igem.org
| Line 53: | Line 53: | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
| - | <td style="width:200px; text-align:center"><a href="https://2011.igem.org/Team:Paris_Bettencourt/Experiments/SinOp"><img style="width:150px; margin-top:20px;" src="https://static.igem.org/mediawiki/2011/ | + | <td style="width:200px; text-align:center"><a href="https://2011.igem.org/Team:Paris_Bettencourt/Experiments/SinOp"><img style="width:150px; margin-top:20px;" src="https://static.igem.org/mediawiki/2011/a/aa/SinOp-button.png"></a> |
</td> | </td> | ||
<td><b><a href="https://2011.igem.org/Team:Paris_Bettencourt/Experiments/SinOp">Sin Operon</a></b> | <td><b><a href="https://2011.igem.org/Team:Paris_Bettencourt/Experiments/SinOp">Sin Operon</a></b> | ||
Revision as of 00:17, 22 September 2011
Our lab achievements
Preliminary experiments
In the Dubey and Ben-Yehuda paper [1] a set of simple experiments are made to prove the existence of the nanotubes. We tryied to reproduce some of them in order to demonstrate again the existence of these entities as a medium of communication between bacteria, and to be sure we are in the good experimental conditions to produce them and that we can go on with our designs.
We tryied to reproduce the two keystone experiments of the paper: the GFP diffusion, and the antibiotic resistance exchange, with less sucess for the latter.
|
The GFP diffusion experiment is the simplest experiment possible. One Bacillus Subtlis strain that produce GFP is mixed with a wild type strain. If some nanotubes are formed, the GFP will diffuse through the tubes and color the non fluorescent strain. We invite you to visit corresponding the page to learn more about what we did and the results we had. |
|
The antibiotic resistance exchange is a more tricky experiment in which bacteria are shown to exchange resistance enzyme through nanotube and allow the population to survive even though all the cells does not carry the resistence.We invite you to visit corresponding the page to learn more about what we did and the results we had. |
New devices
We designed entirely these new devices. They are usually composed of an emitter, a receptor and an amplifier sub-unit.
|
YFP concentration This design relies on a TetO-array which allow us to concentrate YFP-TetR fusion proteins. |
|
T7 RNA polymerase diffusion In this design, we introduce the use of the T7 polymerase both as the transfer molecule and as the auto-amplification system. |
|
tRNA amber diffusion The tRNA amber is the smallest molecule we are trying to get pass the nanotubes. |
Using bistable switches
During our brainstormings, we noticed several natural or artificial bistable switches that could serve both as a receptor and an auto-amplifier. One molecule carefully chosen could toggle the switch in another position. All we have to do is see if it diffuses through the nanotubes.
|
ComS diffusion We took advantage of a switch already existing in B.Subtilis (the ComK/ComS switch) and tried to see if we could toggle it from one state to the other using molecules diffusing through the nanotubes. |
|
Sin Operon |
Lambda switch
|
Lambda switch |
References
- Intercellular Nanotubes Mediate Bacterial Communication, Dubey and Ben-Yehuda, Cell, available here
