Abstract
The bacterial population of a high-rate, anaerobic, fixed-bed loop reactor treating sulfite evaporator condensate from the pulp industry was studied over a 14-month period. This period was divided into seven cycles that included a startup at the beginning of each cycle. Some 82% of the total biomass was immobilized on and between the porous glass rings filling the reactor. The range of the total number of microorganisms in these biofilms was 2 × 109 to 7 × 109 cells per ml. Enumeration and characterization by microbiological methods and by phase-contrast, epifluorescence, and electron microscopy showed that the samples consisted mainly of the following methanogens: a Methanobacterium sp., a Methanosarcina sp., a Methanobrevibacter sp., and a Methanothrix sp., as well as furfural-degrading sulfate-reducing bacteria resembling Desulfovibrio furfuralis. Viable counts of hydrogenotrophic methanogens were relatively stable (mostly within the range of 3.2 × 108 to 7.5 × 108 cells per ml), but Methanobrevibacter cells increased from <5 to 30% of the total hydrogenotrophic count after transfer of the fixed bed into a second reactor vessel. Acetotrophic methanogens reached their highest numbers of 1.3 × 108 to 2.6 × 108 cells per ml in the last fermentation cycles. They showed a morphological shift from sarcinalike packets in early samples to single coccoid forms in later phases of the fermentation. Furfural-degrading sulfate reducers reached counts of 1 × 107 to 5.8 × 107 cells per ml. The distribution of the chief metabolic groups between free fluid and biofilms was analyzed in the fifth fermentation cycle: 4.5 times more furfural degraders were found in the free fluid than in the biofilms. In contrast, 5.8 times more acetotrophic and 16.6 times more hydrogenotrophic methanogens were found in the biofilms than in the free liquid. The data concerning time shifts of morphotypes among the trophic groups of methanogens corroborated the trends observed by using immunological assays on the same samples.
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- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Brune G., Schoberth S. M., Sahm H. Growth of a strictly anaerobic bacterium on furfural (2-furaldehyde). Appl Environ Microbiol. 1983 Nov;46(5):1187–1192. doi: 10.1128/aem.46.5.1187-1192.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chartrain M., Bhatnagar L., Zeikus J. G. Microbial ecophysiology of whey biomethanation: comparison of carbon transformation parameters, species composition, and starter culture performance in continuous culture. Appl Environ Microbiol. 1987 May;53(5):1147–1156. doi: 10.1128/aem.53.5.1147-1156.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chartrain M., Zeikus J. G. Microbial ecophysiology of whey biomethanation: characterization of bacterial trophic populations and prevalent species in continuous culture. Appl Environ Microbiol. 1986 Jan;51(1):188–196. doi: 10.1128/aem.51.1.188-196.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eighmy T. T., Maratea D., Bishop P. L. Electron microscopic examination of wastewater biofilm formation and structural components. Appl Environ Microbiol. 1983 Jun;45(6):1921–1931. doi: 10.1128/aem.45.6.1921-1931.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goodwin S., Conrad R., Zeikus J. G. Influence of pH on microbial hydrogen metabolism in diverse sedimentary ecosystems. Appl Environ Microbiol. 1988 Feb;54(2):590–593. doi: 10.1128/aem.54.2.590-593.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heine-Dobbernack E., Schoberth S. M., Sahm H. Relationship of Intracellular Coenzyme F(420) Content to Growth and Metabolic Activity of Methanobacterium bryantii and Methanosarcina barkeri. Appl Environ Microbiol. 1988 Feb;54(2):454–459. doi: 10.1128/aem.54.2.454-459.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones W. J., Whitman W. B., Fields R. D., Wolfe R. S. Growth and plating efficiency of methanococci on agar media. Appl Environ Microbiol. 1983 Jul;46(1):220–226. doi: 10.1128/aem.46.1.220-226.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kaspar H. F., Wuhrmann K. Kinetic parameters and relative turnovers of some important catabolic reactions in digesting sludge. Appl Environ Microbiol. 1978 Jul;36(1):1–7. doi: 10.1128/aem.36.1.1-7.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kirsch E. J., Sykes R. M. Anaerobic digestion in biological waste treatment. Prog Ind Microbiol. 1971;9:155–237. [PubMed] [Google Scholar]
- Kobayashi H. A., Conway de Macario E., Williams R. S., Macario A. J. Direct characterization of methanogens in two high-rate anaerobic biological reactors. Appl Environ Microbiol. 1988 Mar;54(3):693–698. doi: 10.1128/aem.54.3.693-698.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee M. J., Zinder S. H. Hydrogen partial pressures in a thermophilic acetate-oxidizing methanogenic coculture. Appl Environ Microbiol. 1988 Jun;54(6):1457–1461. doi: 10.1128/aem.54.6.1457-1461.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lupton F. S., Conrad R., Zeikus J. G. Physiological function of hydrogen metabolism during growth of sulfidogenic bacteria on organic substrates. J Bacteriol. 1984 Sep;159(3):843–849. doi: 10.1128/jb.159.3.843-849.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Macario A. J., Conway de Macario E., Ney U., Schoberth S. M., Sahm H. Shifts in methanogenic subpopulations measured with antibody probes in a fixed-bed loop anaerobic bioreactor treating sulfite evaporator condensate. Appl Environ Microbiol. 1989 Aug;55(8):1996–2001. doi: 10.1128/aem.55.8.1996-2001.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller T. L., Wolin M. J. A serum bottle modification of the Hungate technique for cultivating obligate anaerobes. Appl Microbiol. 1974 May;27(5):985–987. doi: 10.1128/am.27.5.985-987.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robinson R. W., Akin D. E., Nordstedt R. A., Thomas M. V., Aldrich H. C. Light and electron microscopic examinations of methane-producing biofilms from anaerobic fixed-bed reactors. Appl Environ Microbiol. 1984 Jul;48(1):127–136. doi: 10.1128/aem.48.1.127-136.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sahm H. Anaerobic wastewater treatment. Adv Biochem Eng Biotechnol. 1984;29:83–115. doi: 10.1007/BFb0000691. [DOI] [PubMed] [Google Scholar]
- Schönheit P., Moll J., Thauer R. K. Nickel, cobalt, and molybdenum requirement for growth of Methanobacterium thermoautotrophicum. Arch Microbiol. 1979 Oct;123(1):105–107. doi: 10.1007/BF00403508. [DOI] [PubMed] [Google Scholar]
- Shimp R. J., Pfaender F. K. Effects of surface area and flow rate on marine bacterial growth in activated carbon columns. Appl Environ Microbiol. 1982 Aug;44(2):471–477. doi: 10.1128/aem.44.2.471-477.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith M. R., Mah R. A. Growth and methanogenesis by Methanosarcina strain 227 on acetate and methanol. Appl Environ Microbiol. 1978 Dec;36(6):870–879. doi: 10.1128/aem.36.6.870-879.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WOLIN E. A., WOLIN M. J., WOLFE R. S. FORMATION OF METHANE BY BACTERIAL EXTRACTS. J Biol Chem. 1963 Aug;238:2882–2886. [PubMed] [Google Scholar]
- Westermann P., Ahring B. K., Mah R. A. Threshold acetate concentrations for acetate catabolism by aceticlastic methanogenic bacteria. Appl Environ Microbiol. 1989 Feb;55(2):514–515. doi: 10.1128/aem.55.2.514-515.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Widdel F., Pfennig N. Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from saline environments. Description of Desulfobacter postgatei gen. nov., sp. nov. Arch Microbiol. 1981 Jul;129(5):395–400. doi: 10.1007/BF00406470. [DOI] [PubMed] [Google Scholar]
- Xun L., Boone D. R., Mah R. A. Control of the Life Cycle of Methanosarcina mazei S-6 by Manipulation of Growth Conditions. Appl Environ Microbiol. 1988 Aug;54(8):2064–2068. doi: 10.1128/aem.54.8.2064-2068.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zehnder A. J., Huser B. A., Brock T. D., Wuhrmann K. Characterization of an acetate-decarboxylating, non-hydrogen-oxidizing methane bacterium. Arch Microbiol. 1980 Jan;124(1):1–11. doi: 10.1007/BF00407022. [DOI] [PubMed] [Google Scholar]
- Zinder S. H., Cardwell S. C., Anguish T., Lee M., Koch M. Methanogenesis in a Thermophilic (58 degrees C) Anaerobic Digestor: Methanothrix sp. as an Important Aceticlastic Methanogen. Appl Environ Microbiol. 1984 Apr;47(4):796–807. doi: 10.1128/aem.47.4.796-807.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]



