Team:Grenoble/Projet/Intro
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- | < | + | <h1>The Project, Mercuro-Coli</h1> |
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- | <h2> | + | <h2>Introduction :</h2> |
<p> | <p> | ||
- | + | With industries growth, wastes are accumulating and presence of pollutant and toxic products is becoming an international concern. | |
</p> | </p> | ||
<p> | <p> | ||
- | Our | + | Our project is oriented in this problematic, Mercuro-Coli is a mercury biosensor which allows to detect and quantify mercury contained into polluted water. Intended to fieldwork studies, the device should be very easy to used : |
</p> | </p> | ||
+ | <a href="https://static.igem.org/mediawiki/2011/5/58/Dispositif.png"><img src="https://static.igem.org/mediawiki/2011/5/58/Dispositif.png"/></a> | ||
+ | |||
+ | <ul> | ||
+ | <li>deally, the device should be a plate carried into a packaging.</li> | ||
+ | <li>Once unpacked, the sample just has to be added.</li> | ||
+ | <li>Finally, the result would be given by a red strip : its presence testifying that the sample contains mercury and its position on the plate acquainting about the quantity.</li> | ||
+ | </ul> | ||
+ | |||
+ | </div> | ||
+ | |||
+ | <div class="blocbackground"> | ||
+ | |||
+ | <h2>Specifications :</h2> | ||
+ | |||
<p> | <p> | ||
- | + | At the beginning of the project, specifications were defined about the final device. To get a better understanding on how the device should run, those are going to be taken back step by step. | |
</p> | </p> | ||
- | + | <ul> | |
+ | <li>Operating living cell : E. Coli: BW 25 113</li> | ||
+ | <li>Only one type of bacteria :</li> | ||
+ | <p>Once our genetic circuit achieved, it will be introduce to our E. Coli strain. Newly obtained bacteria strain will be then spread on the plate forming a bacteria film on the top of it.</p> | ||
+ | <li>Comparative measure :</li> | ||
+ | </ul> | ||
+ | <table class="nobordure"> | ||
+ | <tr> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2011/8/8d/Toggle3.png"><img src="https://static.igem.org/mediawiki/2011/8/8d/Toggle3.png" alt="" title="" width="400"></a></td> | ||
+ | <td> | ||
+ | <p> | ||
+ | The comparative measure will be made by comparing mercury concentration to IPTG concentration. IPTG concentration will is the reference. | ||
+ | </p> | ||
+ | <p> | ||
+ | So, an IPTG gradient concentration will be made beforehand constituting our scale of quantification. | ||
+ | </p> | ||
+ | </td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <p>By adding uniformly the polluted sample, two different bacteria behaviors will come up depending on the predominant concentration :</p> | ||
</div> | </div> | ||
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+ | <!-- | ||
+ | <div class="blocbackground"> | ||
+ | |||
+ | <h2> Abstract</h2> | ||
+ | |||
+ | <p> | ||
+ | Only ranges of pollutant concentration have been measured in the iGEM competition until now. Our goal is to create a simple and accurate, ready-to-use bioquantifier for heavy metals. Simple enough for an easy visual checking and a routine use in the labs. Our system is inspired from Gardner's work on toggle switch biosystem and from former iGem teams' works on quorum sensing communication. | ||
+ | </p> | ||
+ | <p> | ||
+ | Our purpose is to add a pollutant to a device containing a bacterial layer on an engineered medium. This engineered medium is an IPTG gradient.Add of that pollutant to our system induces a geographical division of the plate into two areas : one where the IPTG concentration prevails, and the other where the pollutant concentration prevails. Toggle switch is a biological network which allows to lock our biosystem in a specific state. We use it here in association with complementary quorum sensing genes : A sender and a receiver. Thus, at the interface between both, the reception of quorum sensing molecules by the receptors will induce the coloration of the bacteria. Finally we will obtain a colored line from which we can get the unknown concentration of pollutant. | ||
+ | </p> | ||
+ | <p> | ||
+ | Up to now the quantification of heavy metals requires complex physical and chemical protocols. We propose a new way of quantifying heavy metals, much easier than these ones. A first step to a pure water for everyone! | ||
+ | </p> | ||
+ | |||
+ | </div> | ||
+ | --> |
Revision as of 22:10, 21 September 2011
The Project, Mercuro-Coli
Introduction :
With industries growth, wastes are accumulating and presence of pollutant and toxic products is becoming an international concern.
Our project is oriented in this problematic, Mercuro-Coli is a mercury biosensor which allows to detect and quantify mercury contained into polluted water. Intended to fieldwork studies, the device should be very easy to used :
- deally, the device should be a plate carried into a packaging.
- Once unpacked, the sample just has to be added.
- Finally, the result would be given by a red strip : its presence testifying that the sample contains mercury and its position on the plate acquainting about the quantity.
Specifications :
At the beginning of the project, specifications were defined about the final device. To get a better understanding on how the device should run, those are going to be taken back step by step.
- Operating living cell : E. Coli: BW 25 113
- Only one type of bacteria :
- Comparative measure :
Once our genetic circuit achieved, it will be introduce to our E. Coli strain. Newly obtained bacteria strain will be then spread on the plate forming a bacteria film on the top of it.
By adding uniformly the polluted sample, two different bacteria behaviors will come up depending on the predominant concentration :