Team:WashU/Saffroninakansynecho

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Our project consisted of three different phases. <br>
Our project consisted of three different phases. <br>
Phase 1: Produce zeaxanthin in our two chosen organisms (<i>E. coli</i> and <i>Synechocystis</i>). <br>
Phase 1: Produce zeaxanthin in our two chosen organisms (<i>E. coli</i> and <i>Synechocystis</i>). <br>
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Phase 2: Overproduce the two genes needed for the conversion of zeaxanthin to crocin and saffranal (ZCD and UGTCs2 proteins). <br>
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Phase 2: Overproduce the two genes needed for the conversion of zeaxanthin to crocin and safranal (ZCD and UGTCs2 proteins). <br>
Phase 3: Synthesize crocin <i> in vivo </i> and characterize its production <br>
Phase 3: Synthesize crocin <i> in vivo </i> and characterize its production <br>
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<a href="/Team:WashU/DesignSynecho"><img src ="http://aux.iconpedia.net/uploads/1782679686.png" width=82px height=82px></a></div>
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<a href="/Team:WashU/Characterization"><img src ="http://aux.iconpedia.net/uploads/1782679686.png" width=82px height=82px></a></div>
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Latest revision as of 01:29, 15 September 2012




Overview

Our project consisted of three different phases.
Phase 1: Produce zeaxanthin in our two chosen organisms (E. coli and Synechocystis).
Phase 2: Overproduce the two genes needed for the conversion of zeaxanthin to crocin and safranal (ZCD and UGTCs2 proteins).
Phase 3: Synthesize crocin in vivo and characterize its production

Saffron in a Kan

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