空肠弯曲杆菌(Campylobacter jejuni)电子传递链的功能、生物发生和调控:一种主要食源性病原体生物能量学的新见解。

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Advances in Microbial Physiology Pub Date : 2019-01-01 Epub Date: 2019-03-08 DOI:10.1016/bs.ampbs.2019.02.003
Aidan J Taylor, David J Kelly
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引用次数: 24

摘要

空肠弯曲杆菌(Campylobacter jejuni)是一种人畜共患的Epsilonproteobacterium,生长在鸟类和哺乳动物的胃肠道中,是世界范围内食源性细菌性肠胃炎的最常见原因。空肠梭菌作为一种对氧敏感的微嗜氧菌,必须在高环境氧张力下生存,适应宿主肠道内的氧气限制,并抵抗宿主的氧化攻击。尽管它的基因组很小,但空肠梭菌是一种多功能和代谢活跃的病原体,具有复杂和高度分支的呼吸链,允许使用除氧外的各种电子供体和替代电子受体,包括富马酸盐、硝酸盐、亚硝酸盐、四硫酸盐和N-或s -氧化物。一些新的酶参与这些电子传递链,包括含钨甲酸脱氢酶,使用黄氧还蛋白而不是NADH的复合物I,面向质周的富马酸还原酶和细胞色素c四硫代酸还原酶。这篇综述介绍了这些不同呼吸链的组成和生物能量学的最新描述,因为它们目前被理解,包括最近的工作,为电子传递到各种替代电子受体过程中的能量守恒提供了新的见解。讨论了电子传递链的合成和组装规律。更深入地了解空肠梭菌呼吸系统的独特特征可能有助于制定控制这一重要病原体的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The function, biogenesis and regulation of the electron transport chains in Campylobacter jejuni: New insights into the bioenergetics of a major food-borne pathogen.

Campylobacter jejuni is a zoonotic Epsilonproteobacterium that grows in the gastrointestinal tract of birds and mammals, and is the most frequent cause of food-borne bacterial gastroenteritis worldwide. As an oxygen-sensitive microaerophile, C. jejuni has to survive high environmental oxygen tensions, adapt to oxygen limitation in the host intestine and resist host oxidative attack. Despite its small genome size, C. jejuni is a versatile and metabolically active pathogen, with a complex and highly branched set of respiratory chains allowing the use of a wide range of electron donors and alternative electron acceptors in addition to oxygen, including fumarate, nitrate, nitrite, tetrathionate and N- or S-oxides. Several novel enzymes participate in these electron transport chains, including a tungsten containing formate dehydrogenase, a Complex I that uses flavodoxin and not NADH, a periplasmic facing fumarate reductase and a cytochrome c tetrathionate reductase. This review presents an updated description of the composition and bioenergetics of these various respiratory chains as they are currently understood, including recent work that gives new insights into energy conservation during electron transport to various alternative electron acceptors. The regulation of synthesis and assembly of the electron transport chains is also discussed. A deeper appreciation of the unique features of the respiratory systems of C. jejuni may be helpful in informing strategies to control this important pathogen.

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来源期刊
Advances in Microbial Physiology
Advances in Microbial Physiology 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
16
期刊介绍: Advances in Microbial Physiology publishes topical and important reviews, interpreting physiology to include all material that contributes to our understanding of how microorganisms and their component parts work. First published in 1967, the editors have always striven to interpret microbial physiology in the broadest context and have never restricted the contents to traditional views of whole cell physiology.
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