Department of Chemistry and Nanoscience, Ewha Womans University, Seoul, Republic of Korea.
Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy, and Department of Chemistry, University of Texas at Austin, Austin, TX, USA.
Nat Chem Biol. 2019 Mar;15(3):295-303. doi: 10.1038/s41589-018-0203-4. Epub 2019 Jan 14.
Gentamicin B (GB), a valuable starting material for the preparation of the semisynthetic aminoglycoside antibiotic isepamicin, is produced in trace amounts by the wild-type Micromonospora echinospora. Though the biosynthetic pathway to GB has remained obscure for decades, we have now identified three hidden pathways to GB production via seven hitherto unknown intermediates in M. echinospora. The narrow substrate specificity of a key glycosyltransferase and the C6'-amination enzymes, in combination with the weak and unsynchronized gene expression of the 2'-deamination enzymes, limits GB production in M. echinospora. The crystal structure of the aminotransferase involved in C6'-amination explains its substrate specificity. Some of the new intermediates displayed similar premature termination codon readthrough activity but with reduced toxicity compared to the natural aminoglycoside G418. This work not only led to the discovery of unknown biosynthetic routes to GB, but also demonstrated the potential to mine new aminoglycosides from nature for drug discovery.
庆大霉素 B(GB)是制备半合成氨基糖苷类抗生素异帕米星的宝贵起始原料,由野生型棘孢小单孢菌微量产生。尽管 GB 的生物合成途径几十年来一直不为人知,但我们现在已经在棘孢小单孢菌中通过七个以前未知的中间体确定了三种生产 GB 的隐藏途径。关键糖基转移酶和 C6′-氨基化酶的狭窄底物特异性,以及 2′-脱氨酶的基因表达弱且不同步,限制了 M. echinospora 中 GB 的产量。参与 C6′-氨基化的氨基转移酶的晶体结构解释了其底物特异性。一些新的中间体显示出类似的提前终止密码子通读活性,但与天然氨基糖苷 G418 相比毒性降低。这项工作不仅发现了未知的 GB 生物合成途径,还展示了从自然界中挖掘新的氨基糖苷类化合物用于药物发现的潜力。