首页> 外文会议>Proceedings of Functional Molecules from Natural Sources >ELUCIDATION OF PATHWAYS FOR ANTIBIOTIC BIOSYNTHESIS IN STREPTOMYCES COELICOLOR A3(2)
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ELUCIDATION OF PATHWAYS FOR ANTIBIOTIC BIOSYNTHESIS IN STREPTOMYCES COELICOLOR A3(2)

机译:在链霉菌A3(2)中阐明抗生素生物合成的抗生素生物合成途径

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Natural sources have proved to be invaluable pools for the discovery of clinically-useful compounds for more than 50 years and represent over two thirds of new antibiotics approved for clinical use in the last 25 years. A wide variety of these naturally-derived compounds are produced by the bacterial genus Streptomyces and related actinobacteria, which are well known for their ability to produce a large number of structurally diverse secondary metabolites. Streptomyces species have been extensively studied in an attempt to understand the biosynthetic processes involved in the formation of these secondary metabolites. This knowledge has already been applied in numerous cases to produce analogues of compounds with promising pharmaceutical properties by combinatorial biosynthesis or mutasynthesis approaches.
机译:已经证明,自然来源对于发现临床有用的化合物的宝贵池50多年来,并且代表了超过25年批准的临床使用的三分之二的新抗生素。各种这些天然衍生的化合物是由细菌属的链霉菌和相关的肌动菌产生的,这是众所周知的,其能够产生大量结构不同的次生次生代谢物。已经广泛地研究了肌醇霉菌物种,以试图了解这些次级代谢物形成的生物合成过程。本知识已经应用于许多案例中,以通过组合生物合成或更新的方法产生具有有前途的药物性质的化合物的类似物。

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