Team:Cambridge/Bioluminescence

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{{:Team:Cambridge/Templates/headerbar|colour=#96d446|title=Bioluminescence: Introduction}}
{{:Team:Cambridge/Templates/headerbar|colour=#96d446|title=Bioluminescence: Introduction}}
The Cambridge team for this year's iGEM is aiming to improve the production of light by engineered micro-organisms.  We are pursuing a number of lines of enquiry to achieve this:
The Cambridge team for this year's iGEM is aiming to improve the production of light by engineered micro-organisms.  We are pursuing a number of lines of enquiry to achieve this:
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* <strong>Bacterial luciferases</strong> from <i>Vibrio fischeri</i>, and <i>Photorhabdus luminescens</i>
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* <strong>Bacterial luciferases</strong> from <i>Vibrio fischeri</i>, and <i>Vibrio phosphoreum</i>
* <strong>Firefly luciferases</strong> from <i>Photinus pyralis</i>, and <i>Luciola cruciata</i>, including mutants with increased light output and different colours
* <strong>Firefly luciferases</strong> from <i>Photinus pyralis</i>, and <i>Luciola cruciata</i>, including mutants with increased light output and different colours
* Implementation of the firefly <b>luciferin regenerating enzymes (LRE)</b> from the above species into <i>E. coli</i>, this enzyme is believed to catalyse the recycling of <b>oxyluciferin</b>. We hope it will end the dependence of eukaryotic bioluminescence assays on continual addition of luciferin.
* Implementation of the firefly <b>luciferin regenerating enzymes (LRE)</b> from the above species into <i>E. coli</i>, this enzyme is believed to catalyse the recycling of <b>oxyluciferin</b>. We hope it will end the dependence of eukaryotic bioluminescence assays on continual addition of luciferin.

Revision as of 16:52, 14 August 2010