From peptide precursors to oxazole and thiazole-containing peptide antibiotics: Microcin B17 synthase

被引:246
作者
Li, YM
Milne, JC
Madison, LL
Kolter, R
Walsh, CT
机构
[1] HARVARD UNIV, SCH MED, DEPT BIOL CHEM & MOL PHARMACOL, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, DEPT MICROBIOL & MOL GENET, BOSTON, MA 02115 USA
关键词
D O I
10.1126/science.274.5290.1188
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
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页码:1188 / 1193
页数:6
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