Team:Exeter

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{| style="color:#2F2F4F;background-color:#B9D3EE;" cellpadding="3" cellspacing="1" align="center"
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!align="center"|[[Team:Exeter|Home]]
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!align="center"|[[Team:Exeter/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2013&team_name=Exeter Official Team Profile]
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!align="center"|[[Team:Exeter/Project|Project]]
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!align="center"|[[Team:Exeter/Parts|Part Submissions]]
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!align="center"|[[Team:Exeter/Modelling|Modelling]]
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!align="center"|[[Team:Exeter/Notebook|Notebook]]
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!align="center"|[[Team:Exeter/Safety|Safety]]
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!align="center"|[[Team:Exeter/Attributions|Attributions]]
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[[Image:Exeter_logo.png|right|width=200]] ''Exeter iGEM 2013 are a team comprising of 11 second year undergraduates from the colleges of Engineering, Physics and Biological sciences. Together we plan to engineer E. coli to detect red, green and blue light and produce the correct mix of cyan, magenta and yellow pigments to accurately recreate an exposed image. Our project aims to build a foundation for the precise optical control of biological systems using multiple wavelength light. This has potential in material manufacturing, imaging and will advance our understanding of synthetic biology as a whole.''
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Our wiki is currently in development, if you have any questions for our team, please email igem@ex.ac.uk
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        <h2 style="margin-top:-10px;"> The Microcystin Monster </h2>
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        <p> Algal blooms are an ever-growing problem in freshwater systems. At the Beijing Olympics 2008, 10,000 people were hired to clean up the extensive algal bloom in time for the sailing regatta. The main concern is the level of a toxin called microcystin, which is released by cyanobacteria when they die and lyse. <br><br>
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        Microcystin, a toxin released by Microcystis aeruginosa, is harmful to mammals due to its ability to latch on to the human protein PP1, thus ceasing its operation. We are exploiting the ability of the human protein phosphatase (PP1) to covalently bind to microcystin, in order to develop a biological mop ‘janitor’ to rid algal bloom water of the toxin.</p>
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                          <p><b style="font-size:16px;">Mop</b><br><br> Using <i>B. subtilis</i> and <i>E. coli</i> as chassis to express PP1. This will act as a molecular “mop”.</p>
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                          <p><b style="font-size:16px;">Detector</b><br><br> Engineering the EnvZ and PrkC systems to express GFP or trigger germination in the presence of microcystin.</p>
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                          <p><b style="font-size:16px;">Moptopus</b><br><br>  An electronic sensing device which detects and monitors the state of a freshwater system. It will allow us to predict the likelihood of algal blooms.</p>
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                          <p><b style="font-size:16px;">Human Practices</b><br><br>Current regulations of measuring water quality may not be appropriate. We organised a political campaign to ignite a nationwide debate.</p>
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Revision as of 15:21, 16 August 2013

Home Team Official Team Profile Project Part Submissions Modelling Notebook Safety Attributions


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Exeter iGEM 2013 are a team comprising of 11 second year undergraduates from the colleges of Engineering, Physics and Biological sciences. Together we plan to engineer E. coli to detect red, green and blue light and produce the correct mix of cyan, magenta and yellow pigments to accurately recreate an exposed image. Our project aims to build a foundation for the precise optical control of biological systems using multiple wavelength light. This has potential in material manufacturing, imaging and will advance our understanding of synthetic biology as a whole.

Our wiki is currently in development, if you have any questions for our team, please email igem@ex.ac.uk

Retrieved from "http://2013.igem.org/Team:Exeter"