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氨基糖苷类抗生素:旧药生物合成机制的新见解

Aminoglycoside Antibiotics: New Insights into the Biosynthetic Machinery of Old Drugs.

作者信息

Kudo Fumitaka, Eguchi Tadashi

机构信息

Department of Chemistry, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan.

Department of Chemistry and Materials Science, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro-ku, Tokyo, 152-8551, Japan.

出版信息

Chem Rec. 2016 Feb;16(1):4-18. doi: 10.1002/tcr.201500210. Epub 2015 Oct 12.

Abstract

2-Deoxystreptamine (2DOS) is the unique chemically stable aminocyclitol scaffold of clinically important aminoglycoside antibiotics such as neomycin, kanamycin, and gentamicin, which are produced by Actinomycetes. The 2DOS core can be decorated with various deoxyaminosugars to make structurally diverse pseudo-oligosaccharides. After the discovery of biosynthetic gene clusters for 2DOS-containing aminoglycoside antibiotics, the function of each biosynthetic enzyme has been extensively elucidated. The common biosynthetic intermediates 2DOS, paromamine and ribostamycin are constructed by conserved enzymes encoded in the gene clusters. The biosynthetic intermediates are then converted to characteristic architectures by unique enzymes encoded in each biosynthetic gene cluster. In this Personal Account, we summarize both common biosynthetic pathways and the pathways used for structural diversification.

摘要

2-脱氧链霉胺(2DOS)是临床上重要的氨基糖苷类抗生素如新霉素、卡那霉素和庆大霉素中独特的化学稳定氨基环糖醇骨架,这些抗生素由放线菌产生。2DOS核心可以用各种脱氧氨基糖修饰,以形成结构多样的假寡糖。在发现含2DOS的氨基糖苷类抗生素的生物合成基因簇后,对每种生物合成酶的功能进行了广泛阐明。常见的生物合成中间体2DOS、巴龙胺和核糖霉素由基因簇中编码的保守酶构建。然后,生物合成中间体通过每个生物合成基因簇中编码的独特酶转化为特征性结构。在这篇个人述评中,我们总结了常见的生物合成途径以及用于结构多样化的途径。

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