Effect of 2-bromo-ethane sulfonate, molybdate and chloroform on acetate consumption by methanogenic and sulfate-reducing populations in freshwater sediment

FEMS Microbiology Ecology

Volumn 32, Issue 1, 2000, Pages 35-42

  Scholten, Johannes C M ^a,b,c   Conrad, R ^a   Stams, Alfons J M ^b  

^a MAX PLANCK INSTITUTE FOR TERRESTRIAL MICROBIOLOGY   (Germany)

^b WAGENINGEN UNIVERSITY   (Netherlands)

^c NONE   (United Kingdom)

Author keywords

Acetate; Acetyl CoA pathway; Chloroform; Inhibition; Methanogenesis; Sulfate reduction

Indexed keywords

2 BROMOETHANESULFONIC ACID; ACETIC ACID; CHLOROFORM; MOLYBDIC ACID; PROPIONIC ACID; UNCLASSIFIED DRUG; VALERIC ACID;

ACETATE; FRESHWATER SEDIMENT; METHANOGENIC BACTERIUM; SULFATE-REDUCING BACTERIUM;

ANAEROBIC METABOLISM; ARTICLE; METABOLIC INHIBITION; METHANOBACTERIUM; METHANOGENESIS; MINERALIZATION; PRIORITY JOURNAL; REACTION ANALYSIS; SEDIMENT; SULFATE REDUCING BACTERIUM;

EID: 0034041785     PISSN: 01686496     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-6496(00)00006-4     Document Type: Article

References (44)

1. Capone, D.G. and Kiene, R.P. (1988) Comparison of microbial dynamics in marine and freshwater sediments: contrasts in anaerobic carbon catabolism. Limnol. Oceanogr. 33, 725-749.
2. Hordijk, C.A., Kamminga, H. and Cappenberg, T.E. (1994) Kinetic studies of acetate in freshwater sediments: use of stable isotopic tracers. Geochim. Cosmochim. Acta 58, 683-694.
3. Lovley, D.R. (1982) Intermediary metabolism of organic matter in the sediments of a eutrophic lake. Appl. Environ. Microbiol. 43, 552-560.
4. Parkes, R.J., Gibson, G.R., Mueller-Harvey, I., Buckingham, W.J. and Herbert, R.A. (1989) Determination of the substrates for sulphate-reducing bacteria within marine and estuarine sediments with different rates of sulphate reduction. J. Gen. Microbiol. 135, 175-187.
5. Sørensen, J., Christensen, D. and Jørgensen, B.B. (1981) Volatile fatty acids and hydrogen as substrates for sulphate reducing bacteria in anaerobic marine sediments. Appl. Environ. Microbiol. 42, 5-11.
6. Ward, D.M. and Winfrey, M.R. (1985) Interactions between methanogenic and sulphate reducing bacteria in sediments. Adv. Aquat. Microbiol. 3, 141-179.
7. Smith, R.L. and Klug, M.J. (1981) Electron donors by sulphate-reducing bacteria in eutrophic lake sediments. Appl. Environ. Microbiol. 42, 116-121.
8. Winfrey, M.R. and Zeikus, J.G. (1979) Anaerobic metabolism of immediate methane precursors in Lake Mendota sediments. Appl. Environ. Microbiol. 37, 244-253.
9. Lovley, D.R. and Klug, M.J. (1982) Intermediary metabolism of organic matter in the sediments of a eutrophic lake. Appl. Environ. Microbiol. 43, 187-192.
10. 14C-labeled substrates. Antonie van Leeuwenhoek 40, 457-469.
11. De Graaf, W., Wellsbury, P., Parkes, R.J. and Cappenberg, T.E. (1996) Comparison of acetate turnover in methanogenic and sulphate-reducing sediments by radiolabeling and stable isotope labeling and by use of specific inhibitors: evidence for isotopic exchange. Appl. Environ. Microbiol. 62, 772-777.
12. Nedwell, D.B. (1984) The input and mineralization of organic carbon in anaerobic aquatic sediments. Adv. Microb. Ecol. 7, 93-131.
13. Oremland, R.S. and Capone, D.G. (1988) Use of specific inhibitors in biogeochemistry and microbial ecology. Adv. Microb. Ecol. 10, 285-383.
14. 2 transfer to sulphate and ferric iron-reducing bacteria in acetate consumption in anoxic paddy soil. FEMS Microbiol. Ecol. 16, 61-70.
15. Van Gemerden, H. (1993) Microbial mats: a joint venture. Mar. Geol. 113, 3-25.
16. Scholten, J.C.M. and Stams, A.J.M. (1995) The effect of sulphate and nitrate on methane formation in a freshwater sediment. Antonie van Leeuwenhoek 68, 309-315.
17. Huser, B.A., Wuhrmann, K. and Zehnder, A.J.B. (1982) Methanothrix soehngenii gen. nov. sp. nov., a new acetotrophic non-hydrogen-oxidizing methane bacterium. Arch. Microbiol. 132, 1-9.
18. Wolin, E.A., Wolin, M.J. and Wolfe, R.S. (1963) Formation of methane by bacterial extracts. J. Biol. Chem. 238, 2882-2886.
19. Stams, A.J.M., Van Dijk, J.B., Dijkema, C. and Plugge, C. (1993) Growth of syntrophic propionate-oxidizing bacteria with fumarate in the absence of methanogenic bacteria. Appl. Environ. Microbiol. 59, 1114-1119.
20. Schuler, S. and Conrad, R. (1990) Soils contain two different activities for oxidation of hydrogen. FEMS Microbiol. Ecol. 73, 77-84.
21. Conrad, R., Schütz, H. and Babbel, M. (1987) Temperature limitation of hydrogen turnover and methanogenesis in anoxic paddy soil. FEMS Microbiol. Ecol. 45, 281-289.
22. Krumböck, M. and Conrad, R. (1991) Metabolism of position-labelled glucose in anoxic methanogenic paddy soil and lake sediments. FEMS Microbiol. Ecol. 85, 23-30.
23. Bak, F., Scheff, G. and Janssen, K.H. (1991) A rapid and sensitive ion chromatographic technique for determination of sulphate and sulphate reduction rates in freshwater lake sediment. FEMS Microbiol. Ecol. 85, 23-30.
24. Van Eekert, M.H.A., Schröder, T.J., Stams, A.J.M., Schraa, G. and Field, J.A. (1998) Degradation and fate of carbon tetrachloride in unadapted methanogenic sludge. Appl. Environ. Microbiol. 64, 2350-2356.
25. Scholten, J.C.M. (1994) De invloed van nitraat en sulfaat op de methaanvorming in sedimenten. In: Optimaal Ontwerpen van Proeven bij Enige AIO-projecten (Rasch, D. and Vervuurt, A., Eds.), pp. 51-80. Department of Mathematics, Wageningen (in Dutch).
26. Oude Elferink, S.J.W.H., Visser, A., Hulshoff Pol, L.W. and Stams, A.J.M. (1994) Sulphate reduction in methanogenic bioreactors. FEMS Microbiol. Rev. 15, 119-136.
27. Ingvorsen, K., Zehnder, A.J.B. and Jørgensen, B.B. (1984) Kinetics of sulphate and acetate uptake by Desulfobacter postgatei. Appl. Environ. Microbiol. 47, 403-408.
28. Lovley, D.R. and Klug, M.J. (1986) Model for the distribution of sulphate reduction and methanogenesis in freshwater sediments. Geochim. Cosmochim. Acta 50, 11-18.
29. Widdel, F. (1988) Microbiology and ecology of sulphate- and sulfur-reducing bacteria. In: Biology of Anaerobic Microorganisms (Zehnder, A.J.B., Ed.), pp. 469-585. John Wiley and Sons, New York.
30. Stams, A.J.M. (1994) Metabolic interactions between anaerobic bacteria in methanogenic environments. Antonie van Leeuwenhoek 66, 271-294.
31. Thauer, R.K., Jungermann, K. and Decker, K. (1977) Energy conservation in chemotrophic anaerobic bacteria. Bacteriol. Rev. 41, 100-180.
32. Rothfuss, F. and Conrad, R. (1993) Thermodynamics of methanogenic intermediary metabolism in littoral sediment of lake constance. FEMS Microbiol. Ecol. 12, 265-276.
33. Dolfing, J. (1988) Acetogenesis. In: Biology of Anaerobic Microorganisms (Zehnder, A.J.B., Ed.), pp. 417-468. John Wiley and Sons, New York.
34. Laanbroek, H.J., Abee, T. and Voogd, I.L. (1982) Alcohol conversions by Desulfobulbus propionicus in the presence and absence of sulphate and hydrogen. Arch. Microbiol. 133, 178-184.
35. Conrad, R., Lupton, F.S. and Zeikus, J.G. (1987) Hydrogen metabolism and sulphate-dependent inhibition of methanogenesis in a eutrophic lake sediment (Lake Mendota). FEMS Microbiol. Ecol. 45, 107-115.
36. Krylova, N.I., Janssen, P.H. and Conrad, R. (1997) Turnover of propionate in methanogenic paddy soil. FEMS Microbiol. Ecol. 45, 107-115.
37. Yaday, V.K. and Archer, D.B. (1988) Specific inhibition of sulphate-reducing bacteria in methanogenic co-culture. Lett. Appl. Microbiol. 7, 165-168.
38. Thauer, R.K., Møller-Zinkhan, D. and Spormann, A.M. (1989) Biochemistry of acetate catabolism in anaerobic chemotrophic bacteria. Annu. Rev. Microbiol. 43, 43-67.
39. Ferry, J.G. (1992) Methane from acetate. J. Bacteriol. 174, 5489-5495.
40. 4 and freons 11, 12, and 13 catalyzed by corrinoids. Biochemistry 30, 2713-2719.
41. 12 by Clostridium thermoaceticum. Arch. Biochem. Biophys. 143, 471-484.
42. 2-preincubated cells of Methanobacterium thermoautotrophicum. FEBS Lett. 291 (2), 371-375.
43. 430 from Methanobacterium thermoautotrophicum. Arch. Microbiol. 124, 103-106.
44. Diekert, G. and Wohlfarth, G. (1994) Metabolism of homoacetogens. Antonie van Leeuwenhoek 66, 209-221.