Difference between revisions of "Team:Bordeaux"
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<h6 align="justify" > This year, iGEM Bordeaux proposes an <b> eco-friendly alternative </b> treatment to prevent Downy Mildew: replacing copper sulfate by <b> Curdlan </b>, a sugar biopolymer which <b> stimulates the plant's immune system </b>.<h6> | <h6 align="justify" > This year, iGEM Bordeaux proposes an <b> eco-friendly alternative </b> treatment to prevent Downy Mildew: replacing copper sulfate by <b> Curdlan </b>, a sugar biopolymer which <b> stimulates the plant's immune system </b>.<h6> | ||
<h6 align="justify"> The plant naturally defends itself against pathogens through two distinct levels of immunity, a specific and non specific imunity which both cause a depolarization of the infected cell membrane and triggers the production of antimicrobial metabolites. Curdlan is recognised by the non specific immune system and activates it, with mechanisms similar to modern day vaccines. <h6> | <h6 align="justify"> The plant naturally defends itself against pathogens through two distinct levels of immunity, a specific and non specific imunity which both cause a depolarization of the infected cell membrane and triggers the production of antimicrobial metabolites. Curdlan is recognised by the non specific immune system and activates it, with mechanisms similar to modern day vaccines. <h6> | ||
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<h3 > To sum it up </h3> | <h3 > To sum it up </h3> | ||
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+ | <h6 align="justify"> The production of our molecule will be done using <b> non-pathogenic micro-organisms </b> which can easily be grown in our lab: <i> Escherichia coli </i> and <i> Saccharomyces cerevisiae </i>. These are two microorganisms commonly used in synthetic biology and that are amongst the most well known organisms on the planet. </h6> | ||
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<h6 align ="justify"> We plan on using two host organisms: <i> Sacharomyces cerevisiae </i> which naturally produces Curdlan and <i> Escherichia coli</i>, the most common organism used for synthetic biology. Our bacterial genes and promoters will be synthethized industrially by IDT before being inserted in <i> Escherichia coli </i> whereas for <i> Saccharomyces cerevisiae </i> the gene will be extracted and inserted into a plasmid under the control of a different promoter. These modified cells will then be cultivated to produce our Curdlan molecule in large quantities. The final step of our project will be to extract the curdlan molecule, to optimize our production and to sulfate the molecules if possible since this enhances it's effect on the plant's imune system. </h6> | <h6 align ="justify"> We plan on using two host organisms: <i> Sacharomyces cerevisiae </i> which naturally produces Curdlan and <i> Escherichia coli</i>, the most common organism used for synthetic biology. Our bacterial genes and promoters will be synthethized industrially by IDT before being inserted in <i> Escherichia coli </i> whereas for <i> Saccharomyces cerevisiae </i> the gene will be extracted and inserted into a plasmid under the control of a different promoter. These modified cells will then be cultivated to produce our Curdlan molecule in large quantities. The final step of our project will be to extract the curdlan molecule, to optimize our production and to sulfate the molecules if possible since this enhances it's effect on the plant's imune system. </h6> | ||
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Revision as of 14:17, 30 July 2015