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抗生素自我免疫 tRNA 合成酶在植物肿瘤生物防治剂中的结构特征。

Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent.

机构信息

Department of Cell Biology and Physiology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7090, USA.

European Molecular Biology Laboratory, Grenoble Outstation and Unit of Virus Host-Cell Interactions, UJF-EMBL-CNRS, UMI 3265, 71, Avenue des Martyrs, CS 90181, 38042 Grenoble Cedex 96 rue Jules Horowitz, BP181, Grenoble Cedex 9 38042, France.

出版信息

Nat Commun. 2016 Oct 7;7:12928. doi: 10.1038/ncomms12928.

Abstract

Antibiotic-producing microbes evolved self-resistance mechanisms to avoid suicide. The biocontrol Agrobacterium radiobacter K84 secretes the Trojan Horse antibiotic agrocin 84 that is selectively transported into the plant pathogen A. tumefaciens and processed into the toxin TM84. We previously showed that TM84 employs a unique tRNA-dependent mechanism to inhibit leucyl-tRNA synthetase (LeuRS), while the TM84-producer prevents self-poisoning by expressing a resistant LeuRS AgnB2. We now identify a mechanism by which the antibiotic-producing microbe resists its own toxin. Using a combination of structural, biochemical and biophysical approaches, we show that AgnB2 evolved structural changes so as to resist the antibiotic by eliminating the tRNA-dependence of TM84 binding. Mutagenesis of key resistance determinants results in mutants adopting an antibiotic-sensitive phenotype. This study illuminates the evolution of resistance in self-immunity genes and provides mechanistic insights into a fascinating tRNA-dependent antibiotic with applications for the development of anti-infectives and the prevention of biocontrol emasculation.

摘要

抗生素产生微生物进化出自我抵抗机制以避免自杀。生防菌根瘤农杆菌 K84 分泌木马抗生素农杆菌素 84,它被选择性地运入植物病原体根癌农杆菌,并被加工成毒素 TM84。我们之前表明,TM84 采用独特的 tRNA 依赖性机制抑制亮氨酰-tRNA 合成酶(LeuRS),而 TM84 产生菌通过表达抗性亮氨酰-tRNA 合成酶 AgnB2 来防止自身中毒。现在,我们发现了抗生素产生菌抵抗自身毒素的一种机制。我们使用结构、生化和生物物理方法的组合,表明 AgnB2 发生了结构变化,从而通过消除 TM84 结合的 tRNA 依赖性来抵抗抗生素。关键抗性决定因素的突变导致产生对抗生素敏感的表型的突变体。这项研究阐明了自我免疫基因的抗性进化,并为一种迷人的 tRNA 依赖性抗生素提供了机制见解,该抗生素可用于开发抗感染药物和防止生防去雄。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46b7/5059758/3ba5e71bfc90/ncomms12928-f1.jpg

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