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. 1983 Sep;46(3):728–737. doi: 10.1128/aem.46.3.728-737.1983

Mesophilic Cellulolytic Clostridia from Freshwater Environments

S B Leschine 1, E Canale-Parola 1
PMCID: PMC239342  PMID: 16346388

Abstract

Eight strains of obligately anaerobic, mesophilic, cellulolytic bacteria were isolated from mud of freshwater environments. The isolates (C strains) were rod-shaped, gram negative, and formed terminal spherical to oval spores that swelled the sporangium. The guanine plus cytosine content of the DNA of the C strains ranged from 30.7 to 33.2 mol% (midpoint of thermal denaturation). The C strains fermented cellulose with formation primarily of acetate, ethanol, CO2, and H2. Reducing sugars accumulated in the supernatant fluid of cultures which initially contained ≥0.4% (wt/vol) cellulose. The C strains resembled Clostridium cellobioparum in some phenotypic characteristics and Clostridium papyrosolvens in others, but they were not identical to either of these species. The C strains differed from thermophilic cellulolytic clostridia (e.g., Clostridium thermocellum) not only in growth temperature range but also because they fermented xylan and five-carbon products of plant polysaccharide hydrolysis such as d-xylose and l-arabinose. At 40°C, cellulose was degraded by cellulolytic mesophilic cells (strain C7) at a rate comparable to that at which C. thermocellum degrades cellulose at 60°C. Substrate utilization and growth temperature data indicated that the C strains contribute to the anaerobic breakdown of plant polymers in the environments they inhabit.

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Selected References

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  1. Cooney C. L. Thermophilic anaerobic digestion of solid waste for fuel gas production. Biotechnol Bioeng. 1975 Aug;17(8):1119–1135. doi: 10.1002/bit.260170804. [DOI] [PubMed] [Google Scholar]
  2. Ebersold H. R., Cordier J. L., Lüthy P. Bacterial mesosomes: method dependent artifacts. Arch Microbiol. 1981 Sep;130(1):19–22. doi: 10.1007/BF00527066. [DOI] [PubMed] [Google Scholar]
  3. Giallo J., Gaudin C., Belaich J. P., Petitdemange E., Caillet-Mangin F. Metabolism of glucose and cellobiose by cellulolytic mesophilic Clostridium sp. strain H10. Appl Environ Microbiol. 1983 Mar;45(3):843–849. doi: 10.1128/aem.45.3.843-849.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. HUNGATE R. E. The anaerobic mesophilic cellulolytic bacteria. Bacteriol Rev. 1950 Mar;14(1):1–49. doi: 10.1128/br.14.1.1-49.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Harwood C. S., Canale-Parola E. Branched-chain amino acid fermentation by a marine spirochete: strategy for starvation survival. J Bacteriol. 1981 Oct;148(1):109–116. doi: 10.1128/jb.148.1.109-116.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hungate R. E. Studies on Cellulose Fermentation: I. The Culture and Physiology of an Anaerobic Cellulose-digesting Bacterium. J Bacteriol. 1944 Nov;48(5):499–513. doi: 10.1128/jb.48.5.499-513.1944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Johnson J. L., Francis B. S. Taxonomy of the Clostridia: ribosomal ribonucleic acid homologies among the species. J Gen Microbiol. 1975 Jun;88(2):229–244. doi: 10.1099/00221287-88-2-229. [DOI] [PubMed] [Google Scholar]
  8. McBEE R. H. The anaerobic thermophilic cellulolytic bacteria. Bacteriol Rev. 1950 Mar;14(1):51–63. doi: 10.1128/br.14.1.51-63.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. Ng T. K., Ben-Bassat A., Zeikus J. G. Ethanol Production by Thermophilic Bacteria: Fermentation of Cellulosic Substrates by Cocultures of Clostridium thermocellum and Clostridium thermohydrosulfuricum. Appl Environ Microbiol. 1981 Jun;41(6):1337–1343. doi: 10.1128/aem.41.6.1337-1343.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ng T. K., Weimer T. K., Zeikus J. G. Cellulolytic and physiological properties of Clostridium thermocellum. Arch Microbiol. 1977 Jul 26;114(1):1–7. doi: 10.1007/BF00429622. [DOI] [PubMed] [Google Scholar]
  12. Ng T. K., Zeikus J. G. Comparison of Extracellular Cellulase Activities of Clostridium thermocellum LQRI and Trichoderma reesei QM9414. Appl Environ Microbiol. 1981 Aug;42(2):231–240. doi: 10.1128/aem.42.2.231-240.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Paster B. J., Canale-Parola E. Physiological diversity of rumen spirochetes. Appl Environ Microbiol. 1982 Mar;43(3):686–693. doi: 10.1128/aem.43.3.686-693.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sleytr U. B., Glauert A. M. Ultrastructure of the cell walls of two closely related clostridia that possess different regular arrays of surface subunits. J Bacteriol. 1976 May;126(2):869–882. doi: 10.1128/jb.126.2.869-882.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Stanton T. B., Canale-Parola E. Enumeration and selective isolation of rumen spirochetes. Appl Environ Microbiol. 1979 Nov;38(5):965–973. doi: 10.1128/aem.38.5.965-973.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Stanton T. B., Canale-Parola E. Treponema bryantii sp. nov., a rumen spirochete that interacts with cellulolytic bacteria. Arch Microbiol. 1980 Sep;127(2):145–156. doi: 10.1007/BF00428018. [DOI] [PubMed] [Google Scholar]
  17. 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]
  18. Woo D. D., Holt S. C., Leadbetter E. R. Ultrastructure of Bacteroides species: Bacteroides asaccharolyticus, Bacteroides fragilis, Bacteroides melaninogenicus subspecies melaninogenicus, and B. melaninogenicus subspecies intermedius. J Infect Dis. 1979 May;139(5):534–546. doi: 10.1093/infdis/139.5.534. [DOI] [PubMed] [Google Scholar]

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