恶唑
肽
噻唑
化学
酶
生物化学
肽合成
立体化学
作者
Yue-Ming Li,Jill C. Milne,Lara L. Madison,Roberto Kolter,Christopher T. Walsh
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1996-11-15
卷期号:274 (5290): 1188-1193
被引量:236
标识
DOI:10.1126/science.274.5290.1188
摘要
Esherichia coli microcin B17 is a posttranslationally modified peptide that inhibits bacterial DNA gyrase. It contains four oxazole and four thiazole rings and is representative of a broad class of pharmaceutically important natural products with five-membered heterocycles derived from peptide precursors. An in vitro assay was developed to detect heterocycle formation, and an enzyme complex, microcin B17 synthase, was purified and found to contain three proteins, McbB, McbC, and McbD, that convert 14 residues into the eight mono- and bisheterocyclic moieties in vitro that confer antibiotic activity on mature microcin B17. These enzymatic reactions alter the peptide backbone connectivity. The propeptide region of premicrocin is the major recognition determinant for binding and downstream heterocycle formation by microcin B17 synthase. A general pathway for the enzymatic biosynthesis of these heterocycles is formulated.
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