Zumft W G
Lehrstuhl für Mikrobiologie, Universität Fridericiana, Karlsruhe, Germany.
Microbiol Mol Biol Rev. 1997 Dec;61(4):533-616. doi: 10.1128/mmbr.61.4.533-616.1997.
Denitrification is a distinct means of energy conservation, making use of N oxides as terminal electron acceptors for cellular bioenergetics under anaerobic, microaerophilic, and occasionally aerobic conditions. The process is an essential branch of the global N cycle, reversing dinitrogen fixation, and is associated with chemolithotrophic, phototrophic, diazotrophic, or organotrophic metabolism but generally not with obligately anaerobic life. Discovered more than a century ago and believed to be exclusively a bacterial trait, denitrification has now been found in halophilic and hyperthermophilic archaea and in the mitochondria of fungi, raising evolutionarily intriguing vistas. Important advances in the biochemical characterization of denitrification and the underlying genetics have been achieved with Pseudomonas stutzeri, Pseudomonas aeruginosa, Paracoccus denitrificans, Ralstonia eutropha, and Rhodobacter sphaeroides. Pseudomonads represent one of the largest assemblies of the denitrifying bacteria within a single genus, favoring their use as model organisms. Around 50 genes are required within a single bacterium to encode the core structures of the denitrification apparatus. Much of the denitrification process of gram-negative bacteria has been found confined to the periplasm, whereas the topology and enzymology of the gram-positive bacteria are less well established. The activation and enzymatic transformation of N oxides is based on the redox chemistry of Fe, Cu, and Mo. Biochemical breakthroughs have included the X-ray structures of the two types of respiratory nitrite reductases and the isolation of the novel enzymes nitric oxide reductase and nitrous oxide reductase, as well as their structural characterization by indirect spectroscopic means. This revealed unexpected relationships among denitrification enzymes and respiratory oxygen reductases. Denitrification is intimately related to fundamental cellular processes that include primary and secondary transport, protein translocation, cytochrome c biogenesis, anaerobic gene regulation, metalloprotein assembly, and the biosynthesis of the cofactors molybdopterin and heme D1. An important class of regulators for the anaerobic expression of the denitrification apparatus are transcription factors of the greater FNR family. Nitrate and nitric oxide, in addition to being respiratory substrates, have been identified as signaling molecules for the induction of distinct N oxide-metabolizing enzymes.
反硝化作用是一种独特的能量守恒方式,在厌氧、微需氧以及偶尔的有氧条件下,利用氮氧化物作为细胞生物能学的终端电子受体。该过程是全球氮循环的一个重要分支,与固氮作用相反,并且与化能自养、光养、固氮或有机营养代谢相关,但一般与专性厌氧生活无关。反硝化作用在一个多世纪前就被发现,并且一直被认为是细菌独有的特性,现在已在嗜盐和嗜热古菌以及真菌的线粒体中发现,这引发了有趣的进化前景。在斯氏假单胞菌、铜绿假单胞菌、脱氮副球菌、真养产碱菌和球形红杆菌中,反硝化作用的生化特性及相关遗传学取得了重要进展。假单胞菌是单个属中反硝化细菌最大的集合之一,这有利于将它们用作模式生物。单个细菌内大约需要50个基因来编码反硝化装置的核心结构。已发现革兰氏阴性菌的大部分反硝化过程局限于周质,而革兰氏阳性菌的拓扑结构和酶学则不太明确。氮氧化物的激活和酶促转化基于铁、铜和钼的氧化还原化学。生化突破包括两种呼吸型亚硝酸还原酶的X射线结构以及新型酶一氧化氮还原酶和氧化亚氮还原酶的分离,以及通过间接光谱手段对它们的结构表征。这揭示了反硝化酶与呼吸氧还原酶之间意想不到的关系。反硝化作用与基本的细胞过程密切相关,这些过程包括初级和次级转运、蛋白质转运、细胞色素c生物合成、厌氧基因调控、金属蛋白组装以及辅因子钼蝶呤和血红素D1的生物合成。一类重要的反硝化装置厌氧表达调节因子是更大的FNR家族的转录因子。除了作为呼吸底物外,硝酸盐和一氧化氮还被确定为诱导不同氮氧化物代谢酶的信号分子。