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Kane, S. R., Chakicherla, A. Y., Chain, P., Schmidt, R., Shin, M. W., Legler, T. C., Scow, K. M., Larimer, F. W., Lucas, S. M., Richardson, P. M., et al. (2006) · Journal of Bacteriology · doi:10.1128/jb.01259-06 · Cited by 167 · see citing works

Description of Treponema azotonutricium sp. nov. and Treponema primitia sp. nov., the First Spirochetes Isolated from Termite Guts

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Volatile fatty acid cycling in organic-rich marine sediments

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Oxidation of primary aliphatic alcohols by Acetobacterium carbinolicum sp. nov., a homoacetogenic anaerobe

Eichler, B., & Schink, B. (1984) · Archives of Microbiology · doi:10.1007/bf00454917 · Cited by 153 · see citing works

Enrichment and isolation of Acetitomaculum ruminis, gen. nov., sp. nov.: acetogenic bacteria from the bovine rumen

Greening, R. C., & Leedle, J. A. Z. (1989) · Archives of Microbiology · doi:10.1007/bf00416597 · Cited by 151 · see citing works

Kinetics of the simultaneous utilization of sugar mixtures by Escherichia coli in continuous culture

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The formation of acetic acid from carbon dioxide and hydrogen by anaerobic spore-forming bacteria

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Clostridium formicoaceticum nov. spec. Isolation, description and distinction from C. aceticum and C. thermoaceticum

Andreesen, J. R., Gottschalk, G., & Schlegel, H. G. (1970) · Archives of Microbiology · doi:10.1007/bf00409521 · Cited by 150 · see citing works

Growth ofClostridium thermoaceticum on H2/CO2 or CO as energy source

Kerby, R. L., & Zeikus, J. G. (1983) · Current Microbiology · doi:10.1007/bf01567310 · Cited by 144 · see citing works

The carbon isotope biogeochemistry of acetate from a methanogenic marine sediment

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Trends in Basalt and Sediment Core Contamination During IODP Expedition 301

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Acetonema longum gen.nov.sp.nov., an H2/CO2 acetogenic bacterium from the termite, Pterotermes occidentis

Kane, M. D., & Breznak, J. A. (1991) · Archives of Microbiology · doi:10.1007/bf00290979 · Cited by 141 · see citing works

Peptostreptococcus productus strain that grows rapidly with CO as the energy source

Lorowitz, W. H., & Bryant, M. P. (1984) · Applied and Environmental Microbiology · doi:10.1128/aem.47.5.961-964.1984 · Cited by 140 · see citing works

Sulfitobacter mediterraneus sp. nov., a new sulfite-oxidizing member of the α-Proteobacteria

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Potential applications of cutin-derived CuO reaction products for discriminating vascular plant sources in natural environments

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Energetics of Syntrophic Propionate Oxidation in Defined Batch and Chemostat Cocultures

Scholten, J. C. M., & Conrad, R. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.7.2934-2942.2000 · Cited by 138 · see citing works

Oxidative and reductive acetyl CoA/carbon monoxide dehydrogenase pathway in Desulfobacterium autotrophicum

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Haloarcula marismortui (Volcani) sp. nov., nom. rev., an Extremely Halophilic Bacterium from the Dead Sea

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Staleya guttiformis gen. nov., sp. nov. and Sulfitobacter brevis sp. nov., alpha-3-Proteobacteria from hypersaline, heliothermal and meromictic antarctic Ekho Lake.

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Ruminococcus hydrogenotrophicus sp. nov., a new H 2 /CO 2 -utilizing acetogenic bacterium isolated from human feces

Bernalier, A., Willems, A. L., Leclerc, M., Rochet, V., & Collins, M. D. (1996) · Archives of Microbiology · doi:10.1007/s002030050373 · Cited by 133 · see citing works

Ecological consequences of the phylogenetic and physiological diversities of acetogens

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Carbon Isotope Fractionation by Autotrophic Bacteria with Three Different C0 2 Fixation Pathways

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In vitro H2 utilization by a ruminal acetogenic bacterium cultivated alone or in association with an archaea methanogen is stimulated by a probiotic strain of Saccharomyces cerevisiae

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Isolation and characterization of a methyl chloride utilizing, strictly anaerobic bacterium

Traunecker, J., Preu�, A., & Diekert, G. B. (1991) · Archives of Microbiology · doi:10.1007/bf00248720 · Cited by 126 · see citing works

Characterization of microbial processes in deep aquifers of the Fennoscandian Shield

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Acetogenic and Sulfate-Reducing Bacteria Inhabiting the Rhizoplane and Deep Cortex Cells of the Sea Grass Halodule wrightii

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Clostridium pfennigii sp. nov. Uses Methoxyl Groups of Monobenzenoids and Produces Butyrate

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Isolation and characterization of a new, methylotrophic, acidogenic anaerobe, the marburg strain

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Carbon isotope effects associated with autotrophic acetogenesis

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Growth of Pseudomonas aeruginosa in tap water in relation to utilization of substrates at concentrations of a few micrograms per liter

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Temperature and salt addition effects on the solubility behaviour of some phenolic compounds in water

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Desulfotignum phosphitoxidans sp. nov., a new marine sulfate reducer that oxidizes phosphite to phosphate

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Fermentative metabolism of substituted monoaromatic compounds by a bacterial community from anaerobic sediments

Kaiser, J., & Hanselmann, K. W. (1982) · Archives of Microbiology · doi:10.1007/bf00414999 · Cited by 114 · see citing works

Over het verdwijnen van waterstof en koolzuur onder anaerobe voorwaarden

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Geomicrobiology of deep, low organic carbon sediments in the Woodlark Basin, Pacific Ocean

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Extremely halophilic, methylotrophic, anaerobic bacteria

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Methanogenesis at low temperatures by microflora of tundra wetland soil

Kotsyurbenko, O. R., Nozhevnikova, A. N., Soloviova, T. I., & Zavarzin, G. A. (1996) · Antonie van Leeuwenhoek · doi:10.1007/bf00641614 · Cited by 108 · see citing works

Online δ13C analysis of volatile fatty acids in sediment/porewater systems by liquid chromatography-isotope ratio mass spectrometry

Heuer, V. B., Elvert, M., Tille, S., Krummen, M., Prieto-Mollar, X., Hmelo, L. R., & Hinrichs, K. (2006) · Limnology and Oceanography Methods · doi:10.4319/lom.2006.4.346 · Cited by 108 · see citing works

Methane production from bicarbonate and acetate in an anoxic marine sediment

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Clostridium scatologenes strain SL1 isolated as an acetogenic bacterium from acidic sediments.

Küsel, K., Dorsch, T., Acker, G., Stackebrandt, E. S., & Drake, H. L. (2000) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-50-2-537 · Cited by 107 · see citing works

Fluids from the Oceanic Crust Support Microbial Activities within the Deep Biosphere

Engelen, B., Ziegelmüller, K., Wolf, L., Köpke, B., Gittel, A., Cypionka, H., Treude, T., Nakagawa, S., Inagaki, F., Lever, M. A., et al. (2008) · Geomicrobiology Journal · doi:10.1080/01490450701829006 · Cited by 105 · see citing works

Carbon Isotope Fractionation during Acetoclastic Methanogenesis by Methanosaeta concilii in Culture and a Lake Sediment

Penning, H., Claus, P., Casper, P., & Conrad, R. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.00727-06 · Cited by 105 · see citing works

Acetoanaerobium noterae gen. nov., sp. nov.: an Anaerobic Bacterium That Forms Acetate from H2 and CO2

Sleat, R., Mah, R. A., & Robinson, R. W. (1985) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-35-1-10 · Cited by 104 · see citing works

Numbers, biomass and cultivable diversity of microbial populations relate to depth and borehole-specific conditions in groundwater from depths of 4–450 m in Olkiluoto, Finland

Pedersen, K., Arlinger, J., Eriksson, S., Hallbeck, A., Hallbeck, L., & Johansson, J. (2008) · The ISME Journal · doi:10.1038/ismej.2008.43 · Cited by 103 · see citing works

Reworking of amino acid in marine sediments: Stable carbon isotopic composition of amino acids in sediments along the Washington coast

Keil, R. G., & Fogel, M. L. (2001) · Limnology and Oceanography · doi:10.4319/lo.2001.46.1.0014 · Cited by 102 · see citing works

Evidence for methanogenic Archaea and homoacetogenic Bacteria in deep granitic rock aquifers

Kotelnikova, S., & Pedersen, K. (1997) · FEMS Microbiology Reviews · doi:10.1016/s0168-6445(97)00016-8 · Cited by 102 · see citing works

Carbon assimilation pathways in sulfate reducing bacteria. Formate, carbon dioxide, carbon monoxide, and acetate assimilation by Desulfovibrio baarsii

Jansen, K., Thauer, R. K., Widdel, F., & Fuchs, G. (1984) · Archives of Microbiology · doi:10.1007/bf00402132 · Cited by 101 · see citing works

Physiological Ecology of Clostridium glycolicum RD-1, an Aerotolerant Acetogen Isolated from Sea Grass Roots

Küsel, K., Karnholz, A., Trinkwalter, T., Devereux, R., Acker, G., & Drake, H. L. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.10.4734-4741.2001 · Cited by 100 · see citing works

Formation of Dimethylsulfide and Methanethiol from Methoxylated Aromatic Compounds and Inorganic Sulfide by Newly Isolated Anaerobic Bacteria

Bak, F., & Finster, K. W. (1993) · Springer eBooks · doi:10.1007/978-1-4615-2812-8_41 · Cited by 97 · see citing works

Recovery and Analysis of Formyltetrahydrofolate Synthetase Gene Sequences from Natural Populations of Acetogenic Bacteria

Leaphart, A. B., & Lovell, C. R. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.3.1392-1395.2001 · Cited by 97 · see citing works

Competition between the facultatively chemolithotrophic Thiobacillus A2, an obligately chemolithotrophic Thiobacillus and a heterotrophic spirillum for inorganic and organic substrates

Gottschal, J. C., de Vries, S. C., & Kuenen, J. G. (1979) · Archives of Microbiology · doi:10.1007/bf00425062 · Cited by 96 · see citing works

Function of methanofuran, tetrahydromethanopterin, and coenzyme F420 in Archaeoglobus fulgidus

M�ller-Zinkhan, D., B�rner, G., & Thauer, R. K. (1989) · Archives of Microbiology · doi:10.1007/bf00425174 · Cited by 96 · see citing works

Clostridium mayombei sp. nov., an H2/CO2 acetogenic bacterium from the gut of the African soil-feeding termite, Cubitermes speciosus

Kane, M. D., Brauman, A., & Breznak, J. A. (1991) · Archives of Microbiology · doi:10.1007/bf00290980 · Cited by 95 · see citing works

Granulibacter bethesdensis gen. nov., sp. nov., a distinctive pathogenic acetic acid bacterium in the family Acetobacteraceae

Greenberg, D. E., Porcella, S. F., Stock, F., Wong, A., Conville, P. S., Murray, P. R., Holland, S. M., & Zelazny, A. M. (2006) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.64412-0 · Cited by 95 · see citing works

An Experimental Model: Bacterial Specialists and Generalists Competing in Chemostats

Dykhuizen, D. E., & Davies, M. (1980) · Ecology · doi:10.2307/1936839 · Cited by 94 · see citing works

Characterization of methanogenic Archaea and stable isotope fractionation during methane production in the profundal sediment of an oligotrophic lake (Lake Stechlin, Germany)

Conrad, R., Chan, O.-C., Claus, P., & Casper, P. (2007) · Limnology and Oceanography · doi:10.4319/lo.2007.52.4.1393 · Cited by 94 · see citing works

Evidence for chemiosmotic coupling of reductive dechlorination and ATP synthesis in Desulfomonile tiedjei

Mohn, W. W., & Tiedje, J. M. (1991) · Archives of Microbiology · doi:10.1007/bf00245326 · Cited by 93 · see citing works

Anaerobic acetate oxidation to CO2 by Desulfotomaculum acetoxidans

Spormann, A. M., & Thauer, R. K. (1988) · Archives of Microbiology · doi:10.1007/bf00408310 · Cited by 92 · see citing works

Clostridium methoxybenzovorans sp. nov., a new aromatic o-demethylating homoacetogen from an olive mill wastewater treatment digester

Mechichi, T., Labat, M., Patel, B. K. C., Woo, T. H. S., Thomas, P., & Garcia, J. (1999) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-49-3-1201 · Cited by 91 · see citing works

Interrelations between sulfate-reducing and methane-producing bacteria in bottom deposits of a fresh-water lake. II. Inhibition experiments

Cappenberg, T. E. (1974) · Antonie van Leeuwenhoek · doi:10.1007/bf00394388 · Cited by 89 · see citing works

Formation of dimethylsulfide and methanethiol from methoxylated aromatic compounds and inorganic sulfide by newly isolated anaerobic bacteria

Bak, F., Finster, K. W., & Rothfuß, F. (1992) · Archives of Microbiology · doi:10.1007/bf00276773 · Cited by 89 · see citing works

Sporomusa malonica sp. nov., a homoacetogenic bacterium growing by decarboxylation of malonate or succinate

Dehning, I., Stieb, M., & Schink, B. (1989) · Archives of Microbiology · doi:10.1007/bf00416601 · Cited by 88 · see citing works

Genome Analyses of Three Strains of Rhodobacter sphaeroides : Evidence of Rapid Evolution of Chromosome II

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Sporomusa silvacetica sp. nov., an Acetogenic Bacterium Isolated from Aggregated Forest Soil

Kuhner, C. H., Frank, C., GRIEssZHAMMER, A., Schmittroth, M., Acker, G., GossZNER, A., & Drake, H. L. (1997) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-47-2-352 · Cited by 87 · see citing works

Treponema denticola (ex Brumpt 1925) sp. nov., nom. rev., and Identification of New Spirochete Isolates from Periodontal Pockets

Chan, E. C. S., Siboo, R., Keng, T., Psarra, N., Hurley, R., Cheng, S.-L., & Iugovaz, I. (1993) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-43-2-196 · Cited by 87 · see citing works

Reclassification of the only species of the genus Desulfomonas, Desulfomonas pigra, as Desulfovibrio piger comb. nov.

Loubinoux, J., Valente, F. M. A., Pereira, I. A. C., Costa, A., Grimont, P. A. D., & Faou, A. L. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-52-4-1305 · Cited by 87 · see citing works

Acetogenesis from CO2 in an anoxic marine sediment

Hoehler, T. M., Albert, D. B., Alperin, M. J., & Martens, C. S. (1999) · Limnology and Oceanography · doi:10.4319/lo.1999.44.3.0662 · Cited by 82 · see citing works

Fermentative degradation of nonionic surfactants and polyethylene glycol by enrichment cultures and by pure cultures of homoacetogenic and propionate-forming bacteria

Wagener, S., & Schink, B. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.2.561-565.1988 · Cited by 80 · see citing works

Characterization of Two Subsurface H 2 -Utilizing Bacteria, Desulfomicrobium hypogeium sp. nov. and Acetobacterium psammolithicum sp. nov., and Their Ecological Roles

Krumholz, L. R., Harris, S. H., Tay, S. T.-L., & Suflita, J. M. (1999) · Applied and Environmental Microbiology · doi:10.1128/aem.65.6.2300-2306.1999 · Cited by 80 · see citing works

Benzoate Fermentation by the Anaerobic Bacterium Syntrophus aciditrophicus in the Absence of Hydrogen-Using Microorganisms

Elshahed, M. S., & McInerney, M. J. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.12.5520-5525.2001 · Cited by 79 · see citing works

Carbon isotopic fractionation by plankton in the Southern Indian Ocean: relationship between δ of particulate organic carbon and dissolved carbon dioxide

Bentaleb, I., Fontugne, M., Descolas-Gros, C., Girardin, C., Mariotti, A. A., Pierre, C., Brunet, C., & Alain Poisson, B. (1998) · Journal of Marine Systems · doi:10.1016/s0924-7963(98)00028-1 · Cited by 79 · see citing works

New species of psychrophilic acetogens: Acetobacterium bakii sp. nov., A. paludosum sp. nov., A. fimetarium sp. nov.

Kotsyurbenko, O. R., Simankova, M. V., Nozhevnikova, A. N., Zhilina, T. N., Bolotina, N. P., Лысенко, А. М., & Osipov, G. A. (1995) · Archives of Microbiology · doi:10.1007/bf00262200 · Cited by 79 · see citing works

Hydrogen-Dependent Oxygen Reduction by Homoacetogenic Bacteria Isolated from Termite Guts

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Reclassification of Bacteria of the Genus Protomonas Urakami and Komagata 1984 in the Genus Methylobacterium (Patt, Cole, and Hanson) Emend. Green and Bousfield 1983

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Classification of corynebacteria associated with endocarditis (group JK) as Corynebacterium jeikeium sp. nov.

Jackman, P. J. H., Pitcher, D. G., Pelczynska, S., & Borman, P. (1987) · Systematic and Applied Microbiology · doi:10.1016/s0723-2020(87)80060-7 · Cited by 77 · see citing works

Isolation and characterization of a new spore-forming sulfate-reducing bacterium growing by complete oxidation of catechol

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Molecular monitoring of culturable bacteria from deep-sea sediment of the Nankai Trough, Leg 190 Ocean Drilling Program

Toffin, L. M. A. A., Webster, G., Weightman, A. J., Fry, J. C., & Prieur, D. (2004) · FEMS Microbiology Ecology · doi:10.1016/j.femsec.2004.02.009 · Cited by 75 · see citing works

Isolation and Characterization of the Homoacetogenic Thermophilic Bacterium Moorella glycerini sp. nov.

Slobodkin, A. I., Reysenbach, A., Mayer, F., & Wiegel, J. (1997) · International Journal of Systematic Bacteriology · doi:10.1099/00207713-47-4-969 · Cited by 75 · see citing works

Acetogenesis at Low Temperature

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Archaeoglobus fulgidus couples CO oxidation to sulfate reduction and acetogenesis with transient formate accumulation

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Demethylation and degradation of phenylmethylethers by the sulfide-methylating homoacetogenic bacterium strain TMBS 4

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Methanol utilization by a novel thermophilic homoacetogenic bacterium, Moorella mulderi sp. nov., isolated from a bioreactor

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ANAEROBIC DEGRADATION OF CHOLINE I. , Vibrio cholinicus n. sp

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Hydrogen utilization by clostridia in sewage sludge

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The Evolution of Acetyl-CoA Synthase

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Expression profiles of fhs (FTHFS) genes support the hypothesis that spirochaetes dominate reductive acetogenesis in the hindgut of lower termites

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Distribution of culturable microorganisms in Fennoscandian Shield groundwater

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Metabolism of the 18O-methoxy substituent of 3-methoxybenzoic acid and other unlabeled methoxybenzoic acids by anaerobic bacteria

DeWeerd, K. A., Saxena, A., Nagle, D. P., & Suflita, J. M. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.5.1237-1242.1988 · Cited by 67 · see citing works

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Weak influence of paleoenvironmental conditions on the subsurface biosphere of lake Ohrid in the last 515 kaPreprint

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Metabolic controls on nickel isotope fractionation during microbial methanogenesis and acetogenesis

Miyajima, Y., Katayama, T., & Araoka, D. (2026) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2026.05.012 · Cited by 1 · see citing works

Vertical carbon isotope change in acetate in a surface sediment from the northwestern Pacific Ocean

Kaneko, M., Oba, Y., & Naraoka, H. (2010) · Researches in organic geochemistry · doi:10.20612/rog.26.0_73 · Cited by 1 · see citing works

Lokiarchaeon exhibits homoacetogenesisPreprint

Orsi, W. D., Vuillemin, A., Rodriguez, P. C., Coskun, Ö. K., Gomez‐Saez, G. V., Lavik, G., Morholz, V., & Ferdelman, T. G. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/826495 · Cited by 1 · see citing works

Deep Biosphere

Schippers, A. (2016) · Encyclopedia of earth sciences series/Encyclopedia of earth sciences · doi:10.1007/978-94-007-6238-1_51 · Cited by 1 · see citing works

Cell wall components and intact membrane lipids as proxies for investigation of microbial communities in the deep biosphere

Zhu, R. (2014)

Methane concentrations and carbon isotopic compositions of methane in sediment cores from IODP Expedition 301 Site U1301

Lever, M. A., Heuer, V. B., Morono, Y., Masui, N., Schmidt, F., Alperin, M. J., Inagaki, F., Hinrichs, K., & Teske, A. (2010) · Figshare · doi:10.1594/pangaea.737448

In vitro study of microbial carbon cycling in subseafloor sediments

Geowissenschaften, A. F. (2009)

Methane concentration and porewater acetate of sediment cores from the IODP Expedition 301 Site U1301

Lever, M. A., Heuer, V. B., Morono, Y., Masui, N., Schmidt, F., Alperin, M. J., Inagaki, F., Hinrichs, K., & Teske, A. (2010) · Figshare · doi:10.1594/pangaea.737451

Porewater acetate concentrations of sediment cores from IODP Expedition 301 Site U1301

Lever, M. A., Heuer, V. B., Morono, Y., Masui, N., Schmidt, F., Alperin, M. J., Inagaki, F., Hinrichs, K., & Teske, A. (2010) · Figshare · doi:10.1594/pangaea.737450

Deep Biosphere

Schippers, A. (2015) · Springer eBooks · doi:10.1007/978-94-007-6644-0_51-2

Deep Biosphere

Schippers, A. (2014) · Springer eBooks · doi:10.1007/978-94-007-6644-0_51-1

Unraveling Sulfur, Nitrogen Metabolism and Microbial Community Diversity in a High-Temperature Offshore OilfieldPreprint

Wang, B., Deng, S., Wu, W., Chen, R., Zeng, H., Yao, J., Ma, H., Sun, S., She, Y., & Zhang, F. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4119755

Anaerobic microbiology of methylated compounds in Black Sea sediments

Fischer, P. (2023) · doi:10.18174/590641

Distribution of methane-cycling archaea in buried ridge flank sediment: community zonation, activity, and potential environmental drivers

Lever, M. A., Morono, Y., Inagaki, F., & Teske, A. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1710699

Microbial substrate formation via thermal alteration of organic matter in sediments of the Nankai Trough

Kürzinger, V., Heuer, V. B., Hansen, C. T., Bach, W., Gan, S., & Hinrichs, K. (2026) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2026.09.016

Origin and fate of acetate in an acidic fen

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Acetogenesis from CO2 in an anoxic marine sediment

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Acetate-oxidizing sulfate reduction in anoxic marine sediments.

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Acetogenesis in the Energy-Starved Deep Biosphere – A Paradox?

Lever, M. A. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2011.00284 · Cited by 141 · see citing works

Ancient Metabolisms of a Thermophilic Subseafloor Bacterium

Smith, A. R., Mueller, R., Fisk, M. R., & Colwell, F. S. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.764631 · Cited by 5 · see citing works