Suppr超能文献

一种在大环内酯类聚酮抗生素生物合成中携带氨基酸起始单元的天然保护基团策略。

A natural protecting group strategy to carry an amino acid starter unit in the biosynthesis of macrolactam polyketide antibiotics.

机构信息

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

出版信息

J Am Chem Soc. 2011 Nov 16;133(45):18134-7. doi: 10.1021/ja208927r. Epub 2011 Oct 25.

Abstract

Macrolactam antibiotics are an important class of macrocyclic polyketides that contain a unique nitrogen-containing starter unit. In the present study, a set of starter biosynthetic enzymes in the macrolactam antibiotic vicenistatin was characterized. We found that the protection-deprotection strategy of the aminoacyl-ACP intermediate was critical in this system. On the basis of bioinformatics, the described pathway is also proposed as a common method for carrying amino acids in the biosynthesis of other macrolactam antibiotics.

摘要

大环内酯类抗生素是一类重要的大环多酮类化合物,含有独特的含氮起始单元。在本研究中,对大环内酯抗生素威斯塔他汀中的一组起始生物合成酶进行了表征。我们发现,酰基-ACP 中间物的保护-脱保护策略在该系统中至关重要。基于生物信息学,该途径也被描述为在其他大环内酯抗生素生物合成中携带氨基酸的通用方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验