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. 1997 Feb;63(2):403–407. doi: 10.1128/aem.63.2.403-407.1997

Composition and Role of Extracellular Polymers in Methanogenic Granules

M C Veiga, M K Jain, W Wu, R I Hollingsworth, J G Zeikus
PMCID: PMC1389510  PMID: 16535504

Abstract

Methanobacterium formicicum and Methanosarcina mazeii are two prevalent species isolated from an anaerobic granular consortium grown on a fatty acid mixture. The extracellular polysaccharides (EPS) were extracted from Methanobacterium formicicum and Methanosarcina mazeii and from the methanogenic granules to examine their role in granular development. The EPS made up approximately 20 to 14% of the extracellular polymer extracted from the granules, Methanobacterium formicicum, and Methanosarcina mazeii. The EPS produced by Methanobacterium formicicum was composed mainly of rhamnose, mannose, galactose, glucose, and amino sugars, while that produced by Methanosarcina mazeii contained ribose, galactose, glucose, and glucosamine. The same sugars were also present in the EPS produced by the granules. These results indicate that the two methanogens, especially Methanobacterium formicicum, contributed significantly to the production of the extracellular polymer of the anaerobic granules. Growth temperature, substrates (formate and H(inf2)-CO(inf2)), and the key nutrients (nitrogen and phosphate concentrations) affected polymer production by Methanobacterium formicicum.

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Selected References

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  1. Blumenkrantz N., Asboe-Hansen G. New method for quantitative determination of uronic acids. Anal Biochem. 1973 Aug;54(2):484–489. doi: 10.1016/0003-2697(73)90377-1. [DOI] [PubMed] [Google Scholar]
  2. Costerton J. W., Geesey G. G., Cheng K. J. How bacteria stick. Sci Am. 1978 Jan;238(1):86–95. doi: 10.1038/scientificamerican0178-86. [DOI] [PubMed] [Google Scholar]
  3. Hollingsworth R. I., Abe M., Sherwood J. E., Dazzo F. B. Bacteriophage-induced acidic heteropolysaccharide lyases that convert the acidic heteropolysaccharides of Rhizobium trifolii into oligosaccharide units. J Bacteriol. 1984 Nov;160(2):510–516. doi: 10.1128/jb.160.2.510-516.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kenealy W., Zeikus J. G. Influence of corrinoid antagonists on methanogen metabolism. J Bacteriol. 1981 Apr;146(1):133–140. doi: 10.1128/jb.146.1.133-140.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  6. Robinson R. W., Aldrich H. C., Hurst S. F., Bleiweis A. S. Role of the Cell Surface of Methanosarcina mazei in Cell Aggregation. Appl Environ Microbiol. 1985 Feb;49(2):321–327. doi: 10.1128/aem.49.2.321-327.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Shea S. M. Lanthanum staining of the surface coat of cells. Its enhancement by the use of fixatives containing Alcian blue or cetylpyridinium chloride. J Cell Biol. 1971 Dec;51(3):611–620. doi: 10.1083/jcb.51.3.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Sutherland I. W. Bacterial exopolysaccharides. Adv Microb Physiol. 1972;8:143–213. doi: 10.1016/s0065-2911(08)60190-3. [DOI] [PubMed] [Google Scholar]
  9. Thiele Jurgen H., Zeikus J. Gregory. Control of Interspecies Electron Flow during Anaerobic Digestion: Significance of Formate Transfer versus Hydrogen Transfer during Syntrophic Methanogenesis in Flocs. Appl Environ Microbiol. 1988 Jan;54(1):20–29. doi: 10.1128/aem.54.1.20-29.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. 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]
  11. Wu W. M., Hickey R. F., Zeikus J. G. Characterization of metabolic performance of methanogenic granules treating brewery wastewater: role of sulfate-reducing bacteria. Appl Environ Microbiol. 1991 Dec;57(12):3438–3449. doi: 10.1128/aem.57.12.3438-3449.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Wu W., Jain M. K., Zeikus J. G. Formation of Fatty Acid-degrading, anaerobic granules by defined species. Appl Environ Microbiol. 1996 Jun;62(6):2037–2044. doi: 10.1128/aem.62.6.2037-2044.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]

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