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Production of Artemisinic acid using engineered yeast Journal Club I 7 th July 09 David Roche Charles Fracchia
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Summary Introduction Results Concept of feedback Discussion How is it relevant to SB? Conclusions Materials and Methods Identifying the genes involved in Artemisinin production
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Introduction Artemisinin is anti-malarial compound Currently extracted from the wormwood plant – but not efficient or cheap enough Copied the biosynthetic pathways into the yeast
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Materials and Methods Green: engineered pathways Blue: directly upregulated Purple: indirectly upregulated
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Materials and Methods Increased FPP production by upregulating FPP synthases and downregulating to convertases Introduced ADS Cloned P450
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M&M: Identifying the ADS genes They supposed that the enzymes shown in green shared common ancestor enzymes Compared the genes using BLAST and identified one P450 gene with high homology
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Results 5x 2x 50%
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The concept of feedback inhibition/activation Metabolic flux relies on regulation
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Discussion Increase in yield and decrease in production costs General principle can be applied to production of other compounds, e.g. Taxol – an anti cancer drug, which is normally extracted from the Pacific yew tree. Good example of metabolic engineering to give a useful product.
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Discussion Laborious process of specially engineering each step. Not necessarily easily reproducible. To re- engineer for other compounds, must go ‘back to the drawing board.’ Yield optimization and industrial scale-up still required to reduce prices significantly below their current level.
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How is it relevant to SB? Previous strategies in metabolic engineering seem more of an art with experimentation by trial-and-error. Keasling approach to the problem was more in line with the principles of Synthetic Biology, using a logical approach for the design. Used computational modelling to investigate the most efficient mRNA sequence for maximal compound production
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Conclusions Materials and Methods Results Concept of feedback Discussion Duplicate genes Knockout genes Genetic insertion 50% increase for duplication 2x increase for knockout 5x increase for gene insertion Products of a reaction can control their own conversion Engineered approach to metabolic engineering. Basic method can be applied to production of other compounds.
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