Importance of hydrogenotrophic, aceticlastic and methylotrophic methanogenesis for methane production in terrestrial, aquatic and other anoxic environments: A mini review

被引:205
作者
Conrad, Ralf [1 ]
机构
[1] Max Planck Inst Terr Microbiol, Karl Von Frisch Str 10, D-35043 Marburg, Germany
关键词
electron acceptor; fermentation; methanogenic pathway; organic matter degradation; pH; soil microbial community; temperature; Wood-Ljungdahl pathway; SYNTROPHIC ACETATE OXIDATION; ARCHAEAL COMMUNITY STRUCTURE; RICE FIELD SOIL; DIMETHYL SULFIDE; PADDY SOIL; SP NOV; PROFUNDAL SEDIMENT; ELECTRON FLOW; GEN; NOV; MICROBIAL COMMUNITIES;
D O I
10.1016/S1002-0160(18)60052-9
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
Microbial methanogenesis is a major source of the greenhouse gas methane (CH4). It is the final step in the anaerobic degradation of organic matter when inorganic electron acceptors such as nitrate, ferric iron, or sulfate have been depleted. Knowledge of this degradation pathway is important for the creation of mechanistic models, prediction of future CH4 emission scenarios, and development of mitigation strategies. In most anoxic environments, CH4 is produced from either acetate (aceticlastic methanogenesis) or hydrogen (H-2) plus carbon dioxide (CO2) (hydrogenotrophic methanogenesis). Hydrogen can be replaced by other CO2-type methanogenesis, using formate, carbon monoxide (CO), or alcohols as substrates. The ratio of these two pathways is tightly constrained by the stoichiometry of conversion processes. If the degradation of organic matter is complete (e.g., degradation of straw in rice paddies), then fermentation eventually results in production of acetate and H-2 at a ratio of > 67% aceticlastic and < 33% hydrogenotrophic methanogensis. However, acetate production can be favored when heterotrophic or chemolithotrophic acetogenesis is enhanced, and H-2 production can be favored when syntrophic acetate oxidation is enhanced. This typically occurs at low and elevated temperatures, respectively. Thus, temperature can strongly influence the methanogenic pathway, which may range from 100% aceticlastic methanogenesis at low temperatures to 100% hydrogenotrophic methanogenesis at high temperatures. However, if the degradation of organic matter is not complete (e.g., degradation of soil organic matter), the stoichiometry of fermentation is not tightly constrained, resulting, for example, in the preferential production of H-2, followed by hydrogenotrophic methanogenesis. Preferential production of CH4 by either aceticlastic or hydrogenotrophic methanogenesis can also happen if one of the methanogenic substrates is not consumed by methanogens but is, instead, accumulated, volatilized, or utilized otherwise. Methylotrophic methanogens, which can use methanol as a substrate, are widespread, but it is unlikely that methanol is produced in similar quantities as acetate, CO2, and H-2. Methylotrophic methanogenesis is important in saline environments, where compatible solutes are degraded to methyl compounds (trimethyl amine and dimethyl sulfide) and then serve as non-competitive substrates, while acetate and hydrogen are degraded by non-methanogenic processes, e.g., sulfate reduction.
引用
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页码:25 / 39
页数:15
相关论文
共 157 条
[1]   ROLE OF INTERSPECIES H-2 TRANSFER TO SULFATE AND FERRIC IRON-REDUCING BACTERIA IN ACETATE CONSUMPTION IN ANOXIC PADDY SOIL [J].
ACHTNICH, C ;
SCHUHMANN, A ;
WIND, T ;
CONRAD, R .
FEMS MICROBIOLOGY ECOLOGY, 1995, 16 (01) :61-69
[2]   METHANOL PRODUCTION FROM LIGNIN-RELATED SUBSTANCES BY PHANEROCHAETE-CHRYSOSPORIUM [J].
ANDER, P ;
ERIKSSON, MER ;
ERIKSSON, KE .
PHYSIOLOGIA PLANTARUM, 1985, 65 (03) :317-321
[3]  
[Anonymous], PROKARYOTES
[4]  
[Anonymous], 2012, PROKARYOTES PROKARYO, DOI DOI 10.1007/978-3-642-30123-0_59
[5]   Molecular diversity of methanogens and identification of Methanolobus sp as active methylotrophic Archaea in Lonar crater lake sediments [J].
Antony, Chakkiath Paul ;
Murrell, J. Colin ;
Shouche, Yogesh S. .
FEMS MICROBIOLOGY ECOLOGY, 2012, 81 (01) :43-51
[6]   Methane-cycling communities in a permafrost-affected soil on Herschel Island, Western Canadian Arctic: active layer profiling of mcrA and pmoA genes [J].
Barbier, Beatrice A. ;
Dziduch, Isabel ;
Liebner, Susanne ;
Ganzert, Lars ;
Lantuit, Hugues ;
Pollard, Wayne ;
Wagner, Dirk .
FEMS MICROBIOLOGY ECOLOGY, 2012, 82 (02) :287-302
[7]   Methane biogeochemistry and methanogen communities in two northern peatland ecosystems, New York State [J].
Basiliko, N ;
Yavitt, JB ;
Dees, PM ;
Merkel, SM .
GEOMICROBIOLOGY JOURNAL, 2003, 20 (06) :563-577
[8]   Mass spectrometric monitoring of gases (CO2, CH4, O2) in a mesotrophic peat core from Kopparas Mire, Sweden [J].
Beckmann, M ;
Lloyd, D .
GLOBAL CHANGE BIOLOGY, 2001, 7 (02) :171-180
[9]   ACETATE SYNTHESIS FROM H-2 PLUS CO2 BY TERMITE GUT MICROBES [J].
BREZNAK, JA ;
SWITZER, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1986, 52 (04) :623-630
[10]   Methane emissions from wetlands: biogeochemical, microbial, and modeling perspectives from local to global scales [J].
Bridgham, Scott D. ;
Cadillo-Quiroz, Hinsby ;
Keller, Jason K. ;
Zhuang, Qianlai .
GLOBAL CHANGE BIOLOGY, 2013, 19 (05) :1325-1346