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乳链菌肽481:羊毛硫抗生素合成酶活性的体外重建

Lacticin 481: in vitro reconstitution of lantibiotic synthetase activity.

作者信息

Xie Lili, Miller Leah M, Chatterjee Champak, Averin Olga, Kelleher Neil L, van der Donk Wilfred A

机构信息

Department of Chemistry, University of Illinois at Urbana-Champaign, 600 S. Mathews Avenue, Urbana, IL61801, USA.

出版信息

Science. 2004 Jan 30;303(5658):679-81. doi: 10.1126/science.1092600.

Abstract

The lantibiotic lacticin 481 is synthesized on ribosomes as a prepeptide (LctA) and posttranslationally modified to its mature form. These modifications include dehydration of serines and threonines, followed by intramolecular addition of cysteines to the unsaturated amino acids, which generates cyclic thioethers. This process breaks eight chemical bonds and forms six newbonds and is catalyzed by one enzyme, LctM. We have characterized the in vitro activity of LctM, which completely processed a series of LctA mutants, displaying a permissive substrate specificity that holds promise for antibiotic engineering.

摘要

羊毛硫抗生素乳酸乳球菌素481在核糖体上以前肽(LctA)的形式合成,并在翻译后修饰为成熟形式。这些修饰包括丝氨酸和苏氨酸的脱水,随后分子内的半胱氨酸添加到不饱和氨基酸上,从而产生环状硫醚。这个过程会断裂八个化学键并形成六个新键,由一种酶LctM催化。我们已经对LctM的体外活性进行了表征,它能完全加工一系列LctA突变体,显示出一种宽松的底物特异性,这为抗生素工程带来了希望。

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