Team:Cambridge/Bioluminescence/Photinus pyralis
From 2010.igem.org
(Difference between revisions)
(7 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
{{:Team:Cambridge/Templates/headerMinimalprototype}} | {{:Team:Cambridge/Templates/headerMinimalprototype}} | ||
- | {{:Team:Cambridge/Templates/headerbar|colour=#96d446|title= | + | {{:Team:Cambridge/Templates/headerbar|colour=#96d446|linkcolour=#557A25|title=Project Firefly: Photinus pyralis}} |
- | + | <html><div style="float:right; padding-left:50px;"> | |
- | <html><div style="float:right; padding-left:50px | + | <img src="https://static.igem.org/mediawiki/2010/thumb/f/f2/Firefly.jpg/300px-Firefly.jpg"> |
- | <img src="https://static.igem.org/mediawiki/2010/ | + | |
<br /> | <br /> | ||
- | < | + | <i>Photinus pyralis (<a href="http://www.flickr.com/photos/artfarmer/198487523/">source</a>)</i> |
</div> | </div> | ||
</html> | </html> | ||
- | |||
- | + | The luciferase of the North American firefly, ''P. pyralis'', is a tried and tested mechanism for creating bioluminescence. We were aware that a luciferase from this organism was already present in the registry ([http://partsregistry.org/Part:BBa_I712019 BBa_I712019]). We wanted to improve on this by three techniques: | |
+ | * [https://2010.igem.org/Team:Cambridge/Codons Codon optimisation] for expression in E. coli to increase the rate of translation | ||
+ | * Using a mutant with increased substrate affinity | ||
+ | * Parallel use of the Photinus pyralis [https://2010.igem.org/Team:Cambridge/Bioluminescence/Luciferin_Regeneration luciferin regenerating enzyme] to both relieve inhibition by oxyluciferin and increase availability of luciferin. | ||
- | |||
- | |||
- | |||
{{:Team:Cambridge/Templates/footer}} | {{:Team:Cambridge/Templates/footer}} |
Latest revision as of 09:46, 18 October 2010
Project Firefly: Photinus pyralis
Photinus pyralis (source)
The luciferase of the North American firefly, P. pyralis, is a tried and tested mechanism for creating bioluminescence. We were aware that a luciferase from this organism was already present in the registry ([http://partsregistry.org/Part:BBa_I712019 BBa_I712019]). We wanted to improve on this by three techniques:
- Codon optimisation for expression in E. coli to increase the rate of translation
- Using a mutant with increased substrate affinity
- Parallel use of the Photinus pyralis luciferin regenerating enzyme to both relieve inhibition by oxyluciferin and increase availability of luciferin.