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抗生素博特霉素 D 的结构与生物合成。

Structure and biosynthesis of the antibiotic bottromycin D.

机构信息

Pharmaceutical Sciences Division, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.

出版信息

Org Lett. 2012 Oct 5;14(19):5050-3. doi: 10.1021/ol3022758. Epub 2012 Sep 17.

DOI:10.1021/ol3022758
PMID:22984777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3466018/
Abstract

Drug resistant infectious diseases are quickly becoming a global health crisis. While Streptomyces spp. have been a major source of antibiotics over the past 50 years, efficient methods are needed to identify new antibiotics and greatly improve the rate of discovery. LCMS-based metabolomics were applied to analyze extracts of 50 Streptomyes spp. Using this methodology, we discovered bottromycin D and used whole genome sequencing to determine its biosynthesis by a ribosomal pathway.

摘要

耐药性传染病迅速成为全球健康危机。虽然链霉菌属在过去 50 年中是抗生素的主要来源,但仍需要有效的方法来识别新的抗生素并极大地提高发现的速度。基于 LCMS 的代谢组学被应用于分析 50 株链霉菌属的提取物。使用这种方法,我们发现了 bottromycin D,并通过全基因组测序确定了其通过核糖体途径合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aea/3466018/352dd4db3a48/ol-2012-022758_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aea/3466018/352dd4db3a48/ol-2012-022758_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aea/3466018/352dd4db3a48/ol-2012-022758_0002.jpg

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