Team:NRP-UEA-Norwich

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NRP-UEA-Norwich iGEM 2013 team.
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Our team is based at the School of Biological Sciences at The Univeristy of East Anglia on the Norwich Research Park
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2009.igem.org/Help:Template/Examples">HERE</a>.
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Team NRP-UEA-Norwich iGEM 2013 are developing a biosensor that will enable the identification of novel antimycin-producing strains of streptomycetes. Antibiotic resistance is a rapidly growing global problem and is being exacerbated by the failure to discover new antibiotics. Antimycins produced by streptomycetes are active against various fungi through inhibition of the final stage of electron transport, and it has also been suggested that modified antimycins could be effective anti-cancer drugs. Building up a library of antimycin gene clusters will broaden known pathway (biosynthetic) diversity with the foresight of facilitating genetic engineering. In the long term, pathways could be engineered to create new variants of antimycin with unique or enhanced properties.
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[[Image:NRP-UEA-Norwich_team.png|right|frame|Your team picture]]
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|align="center"|[[Team:NRP-UEA-Norwich | Team NRP-UEA-Norwich]]
 
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Revision as of 19:16, 24 June 2013

NRP-UEA-Norwich iGEM 2013 team. Our team is based at the School of Biological Sciences at The Univeristy of East Anglia on the Norwich Research Park

NRP-UEA-Norwich logo.png


Team NRP-UEA-Norwich iGEM 2013 are developing a biosensor that will enable the identification of novel antimycin-producing strains of streptomycetes. Antibiotic resistance is a rapidly growing global problem and is being exacerbated by the failure to discover new antibiotics. Antimycins produced by streptomycetes are active against various fungi through inhibition of the final stage of electron transport, and it has also been suggested that modified antimycins could be effective anti-cancer drugs. Building up a library of antimycin gene clusters will broaden known pathway (biosynthetic) diversity with the foresight of facilitating genetic engineering. In the long term, pathways could be engineered to create new variants of antimycin with unique or enhanced properties.



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