scholarly journals Electron Bifurcation and Confurcation in Methanogenesis and Reverse Methanogenesis

2018 ◽  
Vol 9 ◽  
Author(s):  
Zhen Yan ◽  
James G. Ferry
Keyword(s):  
Reverse Methanogenesis

A new intra-aerobic metabolism in the nitrite-dependent anaerobic methane-oxidizing bacterium Candidatus ‘Methylomirabilis oxyfera’

2011 ◽  
Vol 39 (1) ◽  
pp. 243-248 ◽  
Author(s):  
Ming L. Wu ◽  
Katharina F. Ettwig ◽  
Mike S.M. Jetten ◽  
Marc Strous ◽  
Jan T. Keltjens ◽  
...  
Keyword(s):  
Nitric Oxide ◽  
Methane Oxidation ◽  
Current Knowledge ◽  
Methanogenic Archaea ◽  
Anaerobic Methane Oxidation ◽  
Oxidation Pathway ◽  
Sulfate Reducing ◽  
Oxidation Of Methane ◽  
Aerobic Methanotrophs ◽  
Reverse Methanogenesis

Biological methane oxidation proceeds either through aerobic or anaerobic pathways. The newly discovered bacterium Candidatus ‘Methylomirabilis oxyfera’ challenges this dichotomy. This bacterium performs anaerobic methane oxidation coupled to denitrification, but does so in a peculiar way. Instead of scavenging oxygen from the environment, like the aerobic methanotrophs, or driving methane oxidation by reverse methanogenesis, like the methanogenic archaea in sulfate-reducing systems, it produces its own supply of oxygen by metabolizing nitrite via nitric oxide into oxygen and dinitrogen gas. The intracellularly produced oxygen is then used for the oxidation of methane by the classical aerobic methane oxidation pathway involving methane mono-oxygenase. The present mini-review summarizes the current knowledge about this process and the micro-organism responsible for it.

scholarly journals Trace methane oxidation studied in several Euryarchaeota under diverse conditions

Archaea ◽  
2005 ◽  
Vol 1 (5) ◽  
pp. 303-309 ◽  
Author(s):  
James J. Moran ◽  
Christopher H. House ◽  
Katherine H. Freeman ◽  
James G. Ferry
Keyword(s):  
Methane Oxidation ◽  
Methanosarcina Barkeri ◽  
Electron Acceptors ◽  
Anaerobic Oxidation Of Methane ◽  
Methanosarcina Acetivorans ◽  
Sulfate Reducing ◽  
Oxidation Of Methane ◽  
Pure Cultures ◽  
Reverse Methanogenesis ◽  
Electron Carriers

We used13C-labeled methane to document the extent of trace methane oxidation byArchaeoglobus fulgidus,Archaeoglobus lithotrophicus,Archaeoglobus profundus,Methanobacterium thermoautotrophicum,Methanosarcina barkeriandMethanosarcina acetivorans. The results indicate trace methane oxidation during growth varied among different species and among methanogen cultures grown on different substrates. The extent of trace methane oxidation byMb. thermoautotrophicum(0.05 ± 0.04%, ± 2 standard deviations of the methane produced during growth) was less than that byM. barkeri(0.15 ± 0.04%), grown under similar conditions with H2and CO2.Methanosarcina acetivoransoxidized more methane during growth on trimethylamine (0.36 ± 0.05%) than during growth on methanol (0.07 ± 0.03%). This may indicate that, inM. acetivorans, either a methyltransferase related to growth on trimethylamine plays a role in methane oxidation, or that methanol is an intermediate of methane oxidation. Addition of possible electron acceptors (O2, NO3–, SO22–, SO32–) or H2to the headspace did not substantially enhance or diminish methane oxidation inM. acetivoranscultures.Separate growth experiments with FAD and NAD+showed that inclusion of these electron carriers also did not enhance methane oxidation. Our results suggest trace methane oxidized during methanogenesis cannot be coupled to the reduction of these electron acceptors in pure cultures, and that the mechanism by which methane is oxidized in methanogens is independent of H2concentration. In contrast to the methanogens, species of the sulfate-reducing genusArchaeoglobusdid not significantly oxidize methane during growth (oxidizing 0.003 ± 0.01% of the methane provided toA. fulgidus, 0.002 ± 0.009% toA. lithotrophicusand 0.003 ± 0.02% toA. profundus). Lack of observable methane oxidation in the threeArchaeoglobusspecies examined may indicate that methyl-coenzyme M reductase, which is not present in this genus, is required for the anaerobic oxidation of methane, consistent with the “reverse methanogenesis” hypothesis.

scholarly journals High-Quality Draft Genome Sequence of “Candidatus Methanoperedens sp.” Strain BLZ2, a Nitrate-Reducing Anaerobic Methane-Oxidizing Archaeon Enriched in an Anoxic Bioreactor

2017 ◽  
Vol 5 (46) ◽  
Author(s):  
Stefanie Berger ◽  
Jeroen Frank ◽  
Paula Dalcin Martins ◽  
Mike S. M. Jetten ◽  
Cornelia U. Welte
Keyword(s):  
Genome Sequence ◽  
Enrichment Culture ◽  
Draft Genome ◽  
Gene Clusters ◽  
Draft Genome Sequence ◽  
Anaerobic Oxidation Of Methane ◽  
Nitrate Reductase Gene ◽  
High Quality ◽  
Oxidation Of Methane ◽  
Reverse Methanogenesis

ABSTRACT The high-quality draft genome of “Candidatus Methanoperedens sp.” strain BLZ2, a nitrate-reducing archaeon anaerobically oxidizing methane, is presented. The genome was obtained from an enrichment culture and measures 3.74 Mb. It harbors two nitrate reductase gene clusters, an ammonium-forming nitrite reductase, and the complete reverse methanogenesis pathway. Methane that escapes to the atmosphere acts as a potent greenhouse gas. Global methane emissions are mitigated by methanotrophs, which oxidize methane to CO2. “Candidatus Methanoperedens spp.” are unique methanotrophic archaea that can perform nitrate-dependent anaerobic oxidation of methane. A high-quality draft genome sequence of only 85 contigs from this archaeon is presented here.

scholarly journals Reverse Methanogenesis and Respiration in Methanotrophic Archaea

Archaea ◽  
2017 ◽  
Vol 2017 ◽  
pp. 1-22 ◽  
Author(s):  
Peer H. A. Timmers ◽  
Cornelia U. Welte ◽  
Jasper J. Koehorst ◽  
Caroline M. Plugge ◽  
Mike S. M. Jetten ◽  
...  
Keyword(s):  
Methane Oxidation ◽  
Molecular Basis ◽  
Electron Acceptors ◽  
Genome Comparison ◽  
Future Research ◽  
Anaerobic Oxidation Of Methane ◽  
Oxidation Of Methane ◽  
Reverse Methanogenesis ◽  
Methyl Coenzyme M Reductase ◽  
Shed Light

Anaerobic oxidation of methane (AOM) is catalyzed by anaerobic methane-oxidizing archaea (ANME) via a reverse and modified methanogenesis pathway. Methanogens can also reverse the methanogenesis pathway to oxidize methane, but only during net methane production (i.e., “trace methane oxidation”). In turn, ANME can produce methane, but only during net methane oxidation (i.e., enzymatic back flux). Net AOM is exergonic when coupled to an external electron acceptor such as sulfate (ANME-1, ANME-2abc, and ANME-3), nitrate (ANME-2d), or metal (oxides). In this review, the reversibility of the methanogenesis pathway and essential differences between ANME and methanogens are described by combining published information with domain based (meta)genome comparison of archaeal methanotrophs and selected archaea. These differences include abundances and special structure of methyl coenzyme M reductase and of multiheme cytochromes and the presence of menaquinones or methanophenazines. ANME-2a and ANME-2d can use electron acceptors other than sulfate or nitrate for AOM, respectively. Environmental studies suggest that ANME-2d are also involved in sulfate-dependent AOM. ANME-1 seem to use a different mechanism for disposal of electrons and possibly are less versatile in electron acceptors use than ANME-2. Future research will shed light on the molecular basis of reversal of the methanogenic pathway and electron transfer in different ANME types.

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