厌氧甲烷氧化古菌对广谱电子受体的代谢潜力。

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Advances in Microbial Physiology Pub Date : 2022-01-01 DOI:10.1016/bs.ampbs.2022.01.003
Martyna Glodowska, Cornelia U Welte, Julia M Kurth
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引用次数: 6

摘要

甲烷(CH4)是一种强有力的温室气体,对我们目前面临的气候变暖起到了重要作用。微生物在全球CH4循环中发挥重要作用,该循环受甲烷生成厌氧产生和甲烷营养氧化去除之间的平衡控制。近几十年的研究提高了我们对CH4氧化的理解,直到1976年人们才认为这是一个严格的有氧过程。目前已知甲烷厌氧氧化(AOM)耦合硫酸盐还原是海洋生态系统中重要的CH4汇。此外,在2006年发现厌氧CH4氧化也可以耦合到硝酸盐还原(N-DAMO),这表明AOM可能比以前认为的更通用,并与其他电子受体相连。因此,近年来越来越多的研究表明或建议在AOM过程中可以使用替代电子受体,包括FeIII, MnIV, AsV, CrVI, SeVI, SbV, VV和BrV。此外,腐殖质、生物炭和高氯酸盐(ClO4-)也被认为是AOM的中介物质。厌氧甲烷营养古菌,即所谓的ANME古菌,是AOM过程的关键参与者,但我们仍然缺乏对其代谢,电子受体偏好及其与其他微生物群落成员相互作用的深入了解。目前尚不清楚ANME古菌是否能够独立氧化CH4并还原金属电子受体,或通过电子转移到共生伙伴、种间电子转移、纳米线或导电毛。因此,本文就ANME古细菌的生理、代谢灵活性和利用各种电子受体的潜力等方面进行综述和讨论。
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Metabolic potential of anaerobic methane oxidizing archaea for a broad spectrum of electron acceptors.

Methane (CH4) is a potent greenhouse gas significantly contributing to the climate warming we are currently facing. Microorganisms play an important role in the global CH4 cycle that is controlled by the balance between anaerobic production via methanogenesis and CH4 removal via methanotrophic oxidation. Research in recent decades advanced our understanding of CH4 oxidation, which until 1976 was believed to be a strictly aerobic process. Anaerobic oxidation of methane (AOM) coupled to sulfate reduction is now known to be an important sink of CH4 in marine ecosystems. Furthermore, in 2006 it was discovered that anaerobic CH4 oxidation can also be coupled to nitrate reduction (N-DAMO), demonstrating that AOM may be much more versatile than previously thought and linked to other electron acceptors. In consequence, an increasing number of studies in recent years showed or suggested that alternative electron acceptors can be used in the AOM process including FeIII, MnIV, AsV, CrVI, SeVI, SbV, VV, and BrV. In addition, humic substances as well as biochar and perchlorate (ClO4-) were suggested to mediate AOM. Anaerobic methanotrophic archaea, the so-called ANME archaea, are key players in the AOM process, yet we are still lacking deeper understanding of their metabolism, electron acceptor preferences and their interaction with other microbial community members. It is still not clear whether ANME archaea can oxidize CH4 and reduce metallic electron acceptors independently or via electron transfer to syntrophic partners, interspecies electron transfer, nanowires or conductive pili. Therefore, the aim of this review is to summarize and discuss the current state of knowledge about ANME archaea, focusing on their physiology, metabolic flexibility and potential to use various electron acceptors.

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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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