Nothing Special   »   [go: up one dir, main page]

Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1984 Jan;47(1):1–6. doi: 10.1128/aem.47.1.1-6.1984

Methanogenesis from Sucrose by Defined Immobilized Consortia

W Jack Jones 1,*, Jean-Pierre Guyot 1,, Ralph S Wolfe 1
PMCID: PMC239601  PMID: 16346452

Abstract

A bacterial consortium capable of sucrose degradation primarily to CH4 and CO2 was constructed, with acetate as the key methanogenic precursor. In addition, the effect of agar immobilization on the activity of the consortium was determined. The primary fermentative organism, Escherichia coli, produced acetate, formate, H2, and CO2 (known substrates for methanogens), as well as ethanol and lactate, compounds that are not substrates for methanogens. Oxidation of the nonmethanogenic substrates, lactate and ethanol, to acetate was mediated by the addition of Acetobacterium woodii and Desulfovibrio vulgaris. The methanogenic stage was accomplished by the addition of the acetophilic methanogen Methanosarcina barkeri and the hydrogenophilic methanogen Methanobacterium formicicum. Results of studies with low substrate concentrations (0.05 to 0.2% [wt/vol]), a growth-limiting medium, and the five-component consortium indicated efficient conversion (40%) of sucrose carbon to CH4. Significant decreases in yields of CH4 and rates of CH4 production were observed if any component of the consortium was omitted. Approximately 70% of the CH4 generated occurred via acetate. Agar-immobilized cells of the consortium exhibited yields of CH4 and rates of CH4 production from sucrose similar to those of nonimmobilized cells. The rate of CH4 production decreased by 25% when cysteine was omitted from reaction conditions and by 40% when the immobilized consortium was stored for 1 week at 4°C.

Full text

PDF
1

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Balch W. E., Fox G. E., Magrum L. J., Woese C. R., Wolfe R. S. Methanogens: reevaluation of a unique biological group. Microbiol Rev. 1979 Jun;43(2):260–296. doi: 10.1128/mr.43.2.260-296.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Balch W. E., Wolfe R. S. New approach to the cultivation of methanogenic bacteria: 2-mercaptoethanesulfonic acid (HS-CoM)-dependent growth of Methanobacterium ruminantium in a pressureized atmosphere. Appl Environ Microbiol. 1976 Dec;32(6):781–791. doi: 10.1128/aem.32.6.781-791.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baresi L., Mah R. A., Ward D. M., Kaplan I. R. Methanogenesis from acetate: enrichment studies. Appl Environ Microbiol. 1978 Jul;36(1):186–197. doi: 10.1128/aem.36.1.186-197.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bryant M. P., Wolin E. A., Wolin M. J., Wolfe R. S. Methanobacillus omelianskii, a symbiotic association of two species of bacteria. Arch Mikrobiol. 1967;59(1):20–31. doi: 10.1007/BF00406313. [DOI] [PubMed] [Google Scholar]
  5. Chen M., Wolin M. J. Influence of CH4 production by Methanobacterium ruminantium on the fermentation of glucose and lactate by Selenomonas ruminantium. Appl Environ Microbiol. 1977 Dec;34(6):756–759. doi: 10.1128/aem.34.6.756-759.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chung K. T. Inhibitory effects of H2 on growth of Clostridium cellobioparum. Appl Environ Microbiol. 1976 Mar;31(3):342–348. doi: 10.1128/aem.31.3.342-348.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hadzija O. A simple method for the quantitative determination of muramic acid. Anal Biochem. 1974 Aug;60(2):512–517. doi: 10.1016/0003-2697(74)90261-9. [DOI] [PubMed] [Google Scholar]
  8. Iannotti E. L., Kafkewitz D., Wolin M. J., Bryant M. P. Glucose fermentation products in Ruminococcus albus grown in continuous culture with Vibrio succinogenes: changes caused by interspecies transfer of H 2 . J Bacteriol. 1973 Jun;114(3):1231–1240. doi: 10.1128/jb.114.3.1231-1240.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kierstan M., Bucke C. The immobilization of microbial cells, subcellular organelles, and enzymes in calcium alginate gels. Biotechnol Bioeng. 1977 Mar;19(3):387–397. doi: 10.1002/bit.260190309. [DOI] [PubMed] [Google Scholar]
  10. Latham M. J., Wolin M. J. Fermentation of cellulose by Ruminococcus flavefaciens in the presence and absence of Methanobacterium ruminantium. Appl Environ Microbiol. 1977 Sep;34(3):297–301. doi: 10.1128/aem.34.3.297-301.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Laube V. M., Martin S. M. Conversion of Cellulose to Methane and Carbon Dioxide by Triculture of Acetivibrio cellulolyticus, Desulfovibrio sp., and Methanosarcina barkeri. Appl Environ Microbiol. 1981 Sep;42(3):413–420. doi: 10.1128/aem.42.3.413-420.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Scheifinger C. C., Linehan B., Wolin M. J. H2 production by Selenomonas ruminantium in the absence and presence of methanogenic bacteria. Appl Microbiol. 1975 Apr;29(4):480–483. doi: 10.1128/am.29.4.480-483.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Smith P. H., Mah R. A. Kinetics of acetate metabolism during sludge digestion. Appl Microbiol. 1966 May;14(3):368–371. doi: 10.1128/am.14.3.368-371.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. 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]
  15. Weimer P. J., Zeikus J. G. Fermentation of cellulose and cellobiose by Clostridium thermocellum in the absence of Methanobacterium thermoautotrophicum. Appl Environ Microbiol. 1977 Feb;33(2):289–297. doi: 10.1128/aem.33.2.289-297.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Winter J. U., Wolfe R. S. Methane formation from fructose by syntrophic associations of Acetobacterium woodii and different strains of methanogens. Arch Microbiol. 1980 Jan;124(1):73–79. doi: 10.1007/BF00407031. [DOI] [PubMed] [Google Scholar]
  17. Winter J., Wolfe R. S. Complete degradation of carbohydrate to carbon dioxide and methane by syntrophic cultures of Acetobacterium woodii and Methanosarcina barkeri. Arch Microbiol. 1979 Apr;121(1):97–102. doi: 10.1007/BF00409211. [DOI] [PubMed] [Google Scholar]
  18. Wolin M. J. Metabolic interactions among intestinal microorganisms. Am J Clin Nutr. 1974 Nov;27(11):1320–1328. doi: 10.1093/ajcn/27.11.1320. [DOI] [PubMed] [Google Scholar]
  19. Zeikus J. G. The biology of methanogenic bacteria. Bacteriol Rev. 1977 Jun;41(2):514–541. doi: 10.1128/br.41.2.514-541.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES