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四环素生物合成的解码与工程化

Decoding and engineering tetracycline biosynthesis.

作者信息

Pickens Lauren B, Tang Yi

机构信息

Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, 90095, USA.

出版信息

Metab Eng. 2009 Mar;11(2):69-75. doi: 10.1016/j.ymben.2008.10.001. Epub 2008 Oct 22.

Abstract

Tetracyclines have been important agents in combating infectious disease since their discovery in the mid-20th century. Following widespread use, tetracycline resistance mechanisms emerged and continue to create a need for new derivatives that are active against resistant bacterial strains. Semisynthesis has led to second and third generation tetracycline derivatives with enhanced antibiotic activity and pharmacological properties. Recent advancement in understanding of the tetracycline biosynthetic pathway may open the door to broaden the range of tetracycline derivatives and afford analogs that are difficult to access by synthetic chemistry.

摘要

自20世纪中叶被发现以来,四环素一直是对抗传染病的重要药物。随着广泛使用,四环素耐药机制出现并持续产生对活性抗耐药菌株的新衍生物的需求。半合成已产生具有增强抗生素活性和药理特性的第二代和第三代四环素衍生物。最近在四环素生物合成途径理解方面的进展可能为拓宽四环素衍生物范围并提供通过合成化学难以获得的类似物打开大门。

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