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. 1995 Mar;61(3):868–871. doi: 10.1128/aem.61.3.868-871.1995

Clostridium cellulolyticum Viability and Sporulation under Cellobiose Starvation Conditions

A Gehin, E Gelhaye, G Raval, H Petitdemange
PMCID: PMC1388369  PMID: 16534970

Abstract

Depending on the moment of cellobiose starvation, Clostridium cellulolyticum cells behave in different ways. Cells starved during the exponential phase of growth sporulate at 30%, whereas exhaustion of the carbon substrate at the beginning of growth does not provoke cell sporulation. Growth in the presence of excess cellobiose generates 3% spores. The response of C. cellulolyticum to carbon starvation involves changes in proteolytic activities; higher activities (20% protein degradation) corresponded to a higher level of sporulation; lower proteolysis (5%) was observed in cells starved during the beginning of exponential growth, when sporulation was not observed; with an excess of cellobiose, an intermediate value (10%), accompanied by a low level of sporulation, was observed in cells taken at the end of the exponential growth phase. The basal percentage of the protein breakdown in nonstarved culture was 4%. Cells lacking proteolytic activities failed to induce sporulation. High concentrations of cellobiose repressed proteolytic activities and sporulation. The onset of carbon starvation during the growth phase affected the survival response of C. cellulolyticum via the sporulation process and also via cell-cellulose interaction. Cells from the exponential growth phase were more adhesive to filter paper than cells from the stationary growth phase but less than cells from the late stationary growth phase.

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Selected References

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  1. Bhat S., Wallace R. J., Orskov E. R. Adhesion of cellulolytic ruminal bacteria to barley straw. Appl Environ Microbiol. 1990 Sep;56(9):2698–2703. doi: 10.1128/aem.56.9.2698-2703.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Damerau K., St John A. C. Role of Clp protease subunits in degradation of carbon starvation proteins in Escherichia coli. J Bacteriol. 1993 Jan;175(1):53–63. doi: 10.1128/jb.175.1.53-63.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Faure E., Bagnara C., Belaich A., Belaich J. P. Cloning and expression of two cellulase genes of Clostridium cellulolyticum in Escherichia coli. Gene. 1988 May 15;65(1):51–58. doi: 10.1016/0378-1119(88)90416-7. [DOI] [PubMed] [Google Scholar]
  4. Fierobe H. P., Gaudin C., Belaich A., Loutfi M., Faure E., Bagnara C., Baty D., Belaich J. P. Characterization of endoglucanase A from Clostridium cellulolyticum. J Bacteriol. 1991 Dec;173(24):7956–7962. doi: 10.1128/jb.173.24.7956-7962.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Gelhaye E., Gehin A., Petitdemange H. Colonization of Crystalline Cellulose by Clostridium cellulolyticum ATCC 35319. Appl Environ Microbiol. 1993 Sep;59(9):3154–3156. doi: 10.1128/aem.59.9.3154-3156.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gelhaye E., Petitdemange H., Gay R. Adhesion and growth rate of Clostridium cellulolyticum ATCC 35319 on crystalline cellulose. J Bacteriol. 1993 Jun;175(11):3452–3458. doi: 10.1128/jb.175.11.3452-3458.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Goldberg A. L., St John A. C. Intracellular protein degradation in mammalian and bacterial cells: Part 2. Annu Rev Biochem. 1976;45:747–803. doi: 10.1146/annurev.bi.45.070176.003531. [DOI] [PubMed] [Google Scholar]
  8. Gottesman S. Genetics of proteolysis in Escherichia coli*. Annu Rev Genet. 1989;23:163–198. doi: 10.1146/annurev.ge.23.120189.001115. [DOI] [PubMed] [Google Scholar]
  9. Landuyt S. L., Hsu E. J. Preparation of Refractile Spores of Clostridium thermosaccharolyticum Involves a Solventogenic Phase. Appl Environ Microbiol. 1992 Jun;58(6):1797–1800. doi: 10.1128/aem.58.6.1797-1800.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Matin A. The molecular basis of carbon-starvation-induced general resistance in Escherichia coli. Mol Microbiol. 1991 Jan;5(1):3–10. doi: 10.1111/j.1365-2958.1991.tb01819.x. [DOI] [PubMed] [Google Scholar]
  11. Rasmussen M. A., White B. A., Hespell R. B. Improved assay for quantitating adherence of ruminal bacteria to cellulose. Appl Environ Microbiol. 1989 Aug;55(8):2089–2091. doi: 10.1128/aem.55.8.2089-2091.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]

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