Latest revision as of 00:42, 4 October 2012

Biofuels and Bacterial Animations

The Caltech 2012 iGEM team's project focused on manipulating bacteria to degrade stable organic polymers such as lignin and alginate; using these substrates to synthesize biofuels, specifically ethanol; and directing their ATP synthesis mechanism to rely on proteorhodopsin as the source of the proton gradient, freeing NADH to interact in the synthetic pathway. Caltech also collaborated with California Institute of the Arts to create an animation using a plate of E. coli transformed with mCherry plasmid. To learn more about our collaboration, view our Human Practice page.

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-=='''From Biofilms to Biofuel'''==
+<h1>Biofuels and Bacterial Animations</h1>
-[[Image:https://static.igem.org/mediawiki/2012/c/ca/Caltech_Flowchart.png|alt=Project Flowchart|Project Flowchart]]
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+The Caltech 2012 iGEM <a href="https://2012.igem.org/Team:Caltech/Team">team's</a> project focused on manipulating bacteria to <a href="https://2012.igem.org/Team:Caltech/Project#Degradation_Project">degrade</a> stable organic polymers such as lignin and alginate; using these substrates to synthesize biofuels, specifically ethanol; and directing their ATP synthesis mechanism to rely on <a href="https://2012.igem.org/Team:Caltech/Project#Proteorhodopsin_Project">proteorhodopsin</a> as the source of the proton gradient, freeing NADH to interact in the synthetic pathway.  Caltech also collaborated with California Institute of the Arts to create an animation using a plate of E. coli transformed with mCherry plasmid.  To learn more about our collaboration, view our <a href="https://2012.igem.org/Team:Caltech/Human_Practice">Human Practice</a> page.
+</p>
-Caltech’s 2012 iGEM [https://2012.igem.org/Team:Caltech/Team team] aims to manipulate bacteria to [https://2012.igem.org/Team:Caltech/Project#Degradation_Project degrade] stable organic polymers such as lignin and alginate; to use these substrates to [https://2012.igem.org/Team:Caltech/Project#Biofuel_Project synthesize biofuels], specifically biodiesel; and to direct their ATP synthesis mechanism to rely on [https://2012.igem.org/Team:Caltech/Project#Proteorhodopsin_Project proteorhodopsin] as the source of the proton gradient, freeing NADH to interact in the synthetic pathway instead.  We will develop the three facets of the project in different strains of E. coli.  We will then splice the manipulated sequences into one new organism.
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