NEW Drugs from OLD Pathways - Teaching Nature New Tricks

发布时间 :2017-10-24  阅读次数 :1310

报告题目:NEW Drugs from OLD Pathways - Teaching Nature New Tricks

报  告 人:Professor Thomas J. Simpson

                 Alfred Capper Pass Chair of Chemistry

                University of Bristol, UK

                Elected Fellow of the Royal Society

                Elected Fellow of the Royal Society of Edinburgh

报告时间: 10月30日 13:30-15:00

报告地点: 闵行校区生命学院树华多功能厅(800号)

联  系 人:林忆杉 mml@sjtu.edu.cn

 

报告摘要:

Engineering metabolic pathways in microorganisms can provide new antibiotics and other bioactive natural products.The mupirocins, e.g. pseudomonic acid A and thiomarinols isolated from Pseudomonas and Pseudoalteromonas bacteria are antibiotics active against MRSA. Clinical applications are restricted by instability in the former and toxicity in the latter. Using classical biosynthetic methods to understand how they are formed, combined with molecular genetic engineering, novel analogues in which both these limitations can be produced. Similarly, the biosynthetic pathway to the fungal metabolite, tenellin, isolated from Beauvaria bassiana, has been engineered to produce the “extinct” compound, bassianin, and many new compounds for biological evaluation.

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