Team:Evry/Overview/Project

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<h1 color=#000033 >The Sponge Patrol Project</h1>
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<h1> The Sponge Patrol Project</h1>
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Our project is based on the engineering of this bacterium in the <b><FONT COLOR=#996666>microbiome </FONT></b>in order to develop a filtrating system allowing to sense and even degrade pollutants in water
Our project is based on the engineering of this bacterium in the <b><FONT COLOR=#996666>microbiome </FONT></b>in order to develop a filtrating system allowing to sense and even degrade pollutants in water
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                       <FONT color="white"> <h5>Chassis</h5></font>
                       <FONT color="white"> <h5>Chassis</h5></font>
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                         <a href="#chassis"><img class="img-circle" src="https://static.igem.org/mediawiki/2014/7/7e/Chassis_EVRY.png" height="128" width="128" alt="Conference" border="30px" /></a>
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                         <a href="#chassis"><img class="img-circle" src="https://static.igem.org/mediawiki/2014/7/7e/Chassis_EVRY.png" height="128" width="128" alt="Conference" border="30px" style="box-shadow: 0 0 8px rgba(0, 0, 0, .8); "/></a>
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                         <font colors ="white"><h5>Transposons</h5></font>
                         <font colors ="white"><h5>Transposons</h5></font>
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For the third participation to the iGEM competition, we decided to introduce <b><FONT COLOR=#666699>a new chassis </FONT></b>to the competition, which is able to work in depth of oceans through a forceful duo: <b>sponge and bacterium</b>.
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For our third participation in the iGEM competition, we decided to use <b><FONT COLOR=#666699>a new chassis </FONT></b> which is able to work in the depth of oceans through a forceful duo: <b>sponge and bacterium</b>.
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Sponge can filtrate up to 20m3 of water/day/kg making it one of the most powerful filtrating system alive.  
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Sponge can filtrate up to 20m<sup>3</sup> of water/day/kg thus being one of the most powerful existing filtrating system.  
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We focused on the sponge <b><FONT COLOR=#FFCC33>Spongia Officinalis</FONT></b>, which lives in symbiosis with the bacterium: <i><FONT COLOR=#006633>Pseudovibrio denitrificans</font></i>.
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We focused on the sponge <b><FONT COLOR=#FFCC33>Spongia Officinalis</FONT></b>, which lives in episymbiosis with the bacterium: <i><FONT COLOR=#006633>Pseudovibrio denitrificans</font></i>.
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Pseudovibrio denitrificans is a marine bacterium not yet characterize and has never been used in iGEM.  
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Pseudovibrio denitrificans is a marine bacterium which as been not yet characterized and also never been used in iGEM.  
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Likewise, we add Spongia Officinalis, a sponge with impressive features and capacities.  
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Likewise, we bring in the iGEM competition Spongia Officinalis, a sponge with impressive features and capacities.  
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This is why we dedicate a part introducing them.  
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This is why we dedicate a part to introducing them.  
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<a href="https://2014.igem.org/Team:Evry/Biology/Chassis" ><img src="https://static.igem.org/mediawiki/2014/d/db/Chassis_seemore_EVRY.png" style="width:20%;height:20%"/></a>
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<a href="https://2014.igem.org/Team:Evry/Biology/Chassis" ><img src="https://static.igem.org/mediawiki/2014/d/db/Chassis_seemore_EVRY.png" style="width:15%;height:15%"/></a>
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Our synthetic system is based on the bacterium Pseudovibrio denitrificans, which is yet arduous to transform due to its marin origin.
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In order to be able to transform our bacterium with genes of interest, we have created a new backbone enabling us to use <FONT COLOR=#CC6699> <b>the transposon system</b></font> in our bacterium.
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This tool allows to insert genes easily into unknown bacteria.
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<a href="https://2014.igem.org/Team:Evry/Biology/Transposons" ><img src="https://static.igem.org/mediawiki/2014/6/62/Tranposeemore.png" style="width:30%;height:30%"/></a>
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<a href="https://2014.igem.org/Team:Evry/Biology/Transposons" ><img src="https://static.igem.org/mediawiki/2014/6/62/Tranposeemore.png" style="width:10%;height:10%"/></a>
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This year, our team objective is to develop a filtrating system which could allow to sense and could even degrade <b><FONT COLOR=#333300>pollutants</font></b> in the future.  
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This year, our team objective is to develop a filtrating system allowing the sensing and eventually degradation of <b><FONT COLOR=#333300>pollutants</font></b>.  
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For this project, we have chosen to work on elements most great classes of marine pollutants belonging to most important classes of pollutants of the marine environment.
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To achieve that goal, we have chosen to work on the most important classes of marine pollutants: phenols, PCBs, nitrites and heavy metals.  
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Hence, we have chosen to focus on <b>phenols</b>, <b>PCBs</b>, <b>nitrite</b> and <b>heavy metals</b>.
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<a href="https://2014.igem.org/Team:Evry/Biology/ToxicCompounds/" ><b><big> <FONT COLOR=#339999>See here</font></big></b><a>  
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<a href="https://2014.igem.org/Team:Evry/Biology/ToxicCompounds" ><img src="https://static.igem.org/mediawiki/2014/3/31/Targetseemore.png" style="width:5%;height:5%"/></a>
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<h4 id="target"> Philosophy </h4></FONT>
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This year, we decided to include in our project a philosophical reflexion on the methods used in iGEM and in synthetic biology. We observed that there was an important contrast between what synthetic biologists ambition to do — a rational, rigorous design with controlled and predicted results — and how they actually design their biological systems — by trial and error, and tinkering. As students engaged in the practice of synthetic biology, we thought that it was very important to take a critical look at the field, and to question whether design in synthetic biology can truly be compared to engineering, or if it is instead the result of inelegant but efficient kludges.
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Since our project means to use sponges as part of our biosensing agent, we also discussed the ethical issues raised by the modification of an animal's microbiome, and by the use of an animal as a bioremediation tool in potentially toxic areas.
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We also had an important reflexion about the risks inherent to the release of genetically modified organisms in seawater, and tried to assert whether a symbiosis between the bacteria and the sponge could be a safe and efficient biological containment of the engineered micro-organisms.
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<a href="https://2014.igem.org/Team:Evry/Policy_and_Practices/Philosophy" ><img src="https://static.igem.org/mediawiki/2014/f/f5/Livre_see_more.jpg"/></a>
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<h4 id="target"> Model </h4></FONT>
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This year we provided two models of the sponge, and also two sensors models. Concernerning the sponge sponge modethe first model was a flux model of the sponges in one dimension. The second model is a 2D diffusion model. It t  ake into accoun the number and the size of the sponge spore. We also model  two sensor  model. The first one about the PCB and the second one for the phenol. The phonol model acess the biological results
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<a href="https://2014.igem.org/Team:Evry/Model/Sponge" ><img src="https://static.igem.org/mediawiki/2014/b/b7/Model_see_more.jpg"/></a>
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Latest revision as of 03:59, 18 October 2014

IGEM Evry 2014

Overview - Project

The Sponge Patrol Project



Water is the most precious and fragile resource on Earth. However seas and oceans are polluted by a wide range of compounds stemming from human activities. Faced with this issue, our team wants to heighten awareness about environmental pollution and particularly its devastating consequences on the aquatic life. In this line of thinking we are driven to design a bioremediation tool based on the considerable filtration capacity of sponges to decrease the marine pollution and protect aquatic ecosystems. Our project is based on the engineering of this bacterium in the microbiome in order to develop a filtrating system allowing to sense and even degrade pollutants in water


Chassis
Conference
Transposons
Workshops
Target
Hackathons


Chassis


For our third participation in the iGEM competition, we decided to use a new chassis which is able to work in the depth of oceans through a forceful duo: sponge and bacterium. Sponge can filtrate up to 20m3 of water/day/kg thus being one of the most powerful existing filtrating system. We focused on the sponge Spongia Officinalis, which lives in episymbiosis with the bacterium: Pseudovibrio denitrificans.
Pseudovibrio denitrificans is a marine bacterium which as been not yet characterized and also never been used in iGEM.
Likewise, we bring in the iGEM competition Spongia Officinalis, a sponge with impressive features and capacities.
This is why we dedicate a part to introducing them.




Transposons


Our synthetic system is based on the bacterium Pseudovibrio denitrificans, which is yet arduous to transform due to its marin origin. In order to be able to transform our bacterium with genes of interest, we have created a new backbone enabling us to use the transposon system in our bacterium. This tool allows to insert genes easily into unknown bacteria.




Target


This year, our team objective is to develop a filtrating system allowing the sensing and eventually degradation of pollutants. To achieve that goal, we have chosen to work on the most important classes of marine pollutants: phenols, PCBs, nitrites and heavy metals.

Philosophy


This year, we decided to include in our project a philosophical reflexion on the methods used in iGEM and in synthetic biology. We observed that there was an important contrast between what synthetic biologists ambition to do — a rational, rigorous design with controlled and predicted results — and how they actually design their biological systems — by trial and error, and tinkering. As students engaged in the practice of synthetic biology, we thought that it was very important to take a critical look at the field, and to question whether design in synthetic biology can truly be compared to engineering, or if it is instead the result of inelegant but efficient kludges. Since our project means to use sponges as part of our biosensing agent, we also discussed the ethical issues raised by the modification of an animal's microbiome, and by the use of an animal as a bioremediation tool in potentially toxic areas. We also had an important reflexion about the risks inherent to the release of genetically modified organisms in seawater, and tried to assert whether a symbiosis between the bacteria and the sponge could be a safe and efficient biological containment of the engineered micro-organisms.

Model


This year we provided two models of the sponge, and also two sensors models. Concernerning the sponge sponge modethe first model was a flux model of the sponges in one dimension. The second model is a 2D diffusion model. It t ake into accoun the number and the size of the sponge spore. We also model two sensor model. The first one about the PCB and the second one for the phenol. The phonol model acess the biological results