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低调行事:炭疽芽孢杆菌中铁载体petrobactin的非经典生物化学与分子生物学

Flying under the radar: The non-canonical biochemistry and molecular biology of petrobactin from Bacillus anthracis.

作者信息

Hagan A K, Carlson P E, Hanna P C

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, 1150 W. Medical Center Drive, 6703 Medical Science Building II, Ann Arbor, MI, 48109.

Laboratory of Mucosal Pathogens and Cellular Immunity, Division of Bacterial, Parasitic, and Allergenic Products, Office of Vaccines Research and Review, Center for Biologics Evaluation and Research, US Food and Drug Administration, 10903 New Hampshire Avenue, Building 52/72; Rm 3306, Silver Spring, MD, 20993.

出版信息

Mol Microbiol. 2016 Oct;102(2):196-206. doi: 10.1111/mmi.13465. Epub 2016 Aug 9.

Abstract

The dramatic, rapid growth of Bacillus anthracis that occurs during systemic anthrax implies a crucial requirement for the efficient acquisition of iron. While recent advances in our understanding of B. anthracis iron acquisition systems indicate the use of strategies similar to other pathogens, this review focuses on unique features of the major siderophore system, petrobactin. Ways that petrobactin differs from other siderophores include: A. unique ferric iron binding moieties that allow petrobactin to evade host immune proteins; B. a biosynthetic operon that encodes enzymes from both major siderophore biosynthesis classes; C. redundancy in membrane transport systems for acquisition of Fe-petrobactin holo-complexes; and, D. regulation that appears to be controlled predominately by sensing the host-like environmental signals of temperature, CO levels and oxidative stress, as opposed to canonical sensing of intracellular iron levels. We argue that these differences contribute in meaningful ways to B. anthracis pathogenesis. This review will also outline current major gaps in our understanding of the petrobactin iron acquisition system, some projected means for exploiting current knowledge, and potential future research directions.

摘要

在系统性炭疽病期间发生的炭疽芽孢杆菌的显著快速生长意味着高效获取铁的关键需求。虽然我们对炭疽芽孢杆菌铁获取系统的理解最近取得了进展,表明其使用了与其他病原体类似的策略,但本综述重点关注主要铁载体系统——石油杆菌素(petrobactin)的独特特征。石油杆菌素与其他铁载体的不同之处包括:A. 独特的三价铁结合部分,使石油杆菌素能够逃避宿主免疫蛋白;B. 一个生物合成操纵子,编码来自主要铁载体生物合成两类的酶;C. 用于获取铁 - 石油杆菌素全复合物的膜转运系统的冗余;以及D. 调控似乎主要通过感知温度、一氧化碳水平和氧化应激等类似宿主的环境信号来控制,而不是通过对细胞内铁水平的典型感知。我们认为这些差异以有意义的方式促成了炭疽芽孢杆菌的致病性。本综述还将概述我们目前对石油杆菌素铁获取系统理解中的主要差距、一些利用现有知识的预计方法以及潜在的未来研究方向。

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