Anaerobic Metabolism in Haloferax Genus: Denitrification as Case of Study.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Advances in Microbial Physiology Pub Date : 2016-01-01 Epub Date: 2016-03-15 DOI:10.1016/bs.ampbs.2016.02.001
J Torregrosa-Crespo, R M Martínez-Espinosa, J Esclapez, V Bautista, C Pire, M Camacho, D J Richardson, M J Bonete
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引用次数: 31

Abstract

A number of species of Haloferax genus (halophilic archaea) are able to grow microaerobically or even anaerobically using different alternative electron acceptors such as fumarate, nitrate, chlorate, dimethyl sulphoxide, sulphide and/or trimethylamine. This metabolic capability is also shown by other species of the Halobacteriaceae and Haloferacaceae families (Archaea domain) and it has been mainly tested by physiological studies where cell growth is observed under anaerobic conditions in the presence of the mentioned compounds. This work summarises the main reported features on anaerobic metabolism in the Haloferax, one of the better described haloarchaeal genus with significant potential uses in biotechnology and bioremediation. Special attention has been paid to denitrification, also called nitrate respiration. This pathway has been studied so far from Haloferax mediterranei and Haloferax denitrificans mainly from biochemical point of view (purification and characterisation of the enzymes catalysing the two first reactions). However, gene expression and gene regulation is far from known at the time of writing this chapter.

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盐藻属厌氧代谢:以反硝化为例研究。
许多种类的嗜盐古菌能够利用不同的替代电子受体(如富马酸盐、硝酸盐、氯酸盐、二甲基亚砜、硫化物和/或三甲胺)进行微氧甚至厌氧生长。这种代谢能力也显示在其他种类的盐杆菌科和盐藻科(古细菌领域),它主要是通过生理研究,在厌氧条件下观察细胞生长,在上述化合物的存在。本文综述了盐古菌属(Haloferax)在厌氧代谢方面的主要报道特征,盐古菌属是一种在生物技术和生物修复方面具有重要潜在应用前景的菌属。特别注意的是反硝化作用,也称为硝酸盐呼吸作用。迄今为止,对地中海盐铁酸盐和反硝化盐铁酸盐这一途径的研究主要是从生化的角度(纯化和表征催化前两个反应的酶)。然而,在撰写本章时,基因表达和基因调控还远远不为人所知。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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.
期刊最新文献
Preface. Biological functions of bacterial lysophospholipids. Redefining the bacterial Type I protein secretion system. Purine catabolism by enterobacteria. Fumarate, a central electron acceptor for Enterobacteriaceae beyond fumarate respiration and energy conservation.
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