Team:Cambridge

From 2010.igem.org

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We are the  Cambridge Team for iGEM 2010. Over the course of the summer we have built a number of BioBricks to allow <strong>bioluminescence</strong>. We used genes originally found in fireflies (<em>Photinus pyralis</em> and <em>Luciola cruciata</em>) and those from the marine bacterium <em>Vibrio fischeri</em>.
We are the  Cambridge Team for iGEM 2010. Over the course of the summer we have built a number of BioBricks to allow <strong>bioluminescence</strong>. We used genes originally found in fireflies (<em>Photinus pyralis</em> and <em>Luciola cruciata</em>) and those from the marine bacterium <em>Vibrio fischeri</em>.
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* Mutagenesis to create a number of [https://2010.igem.org/Team:Cambridge/Bioluminescence/Colour '''different colours''']
* Mutagenesis to create a number of [https://2010.igem.org/Team:Cambridge/Bioluminescence/Colour '''different colours''']
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We complemented these firefly systems, which require the addition of the substrate luciferin, with light producing systems from '''Vibrio fischeri'''.  We believe we have created the '''first''' biobrick to emit light in normal E. coli strains without the addition of any luciferin substrate.
We complemented these firefly systems, which require the addition of the substrate luciferin, with light producing systems from '''Vibrio fischeri'''.  We believe we have created the '''first''' biobrick to emit light in normal E. coli strains without the addition of any luciferin substrate.
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We codon optimised the bacterial lux operon in an attempt to lift [https://2010.igem.org/Team:Cambridge/Bioluminescence/Bacterial_Codon_optimisation '''hns repression''']
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These systems will form the basis of simple quantitative assays and in the future might also be used as a light source.
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Over the summer we constructed a number of tools to assist the synthetic biologists of the future:
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* '''[https://2010.igem.org/Team:Cambridge/Tools/Gibson Gibthon]''' allows the user to enter a series of BioBrick or GenBank IDs in a specific order and computes the appropriate primers for [https://2010.igem.org/Team:Cambridge/Gibson/Introduction '''Gibson Assembly'''].
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We have also designed a number of software tools to assist synthetic biologists, including a primer design tool for Gibson Assembly.
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* [https://2010.igem.org/Team:Cambridge/Tools/GenBank BioBrick → GenBank] allows parts from the registry to be downloaded in .gb format, making them '''compatible''' with a wide range of biological software.
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* The [https://2010.igem.org/Team:Cambridge/Tools/Eglometer '''E.glometer'''] is a cheap, easily built, piece of electronics for measuring bioluminescence.  It allows scientists without access to expensive plate readers to measure bioluminescence.
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This page will be updated over the course of the summer as we progress through our project. If you would like to get in touch with us for any reason, please do [mailto:info@cambridgeigem.org email us].
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Revision as of 16:01, 25 October 2010