Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1993 Jul;59(7):2286–2292. doi: 10.1128/aem.59.7.2286-2292.1993

Biodegradation of ortho-cresol by a mixed culture of nitrate-reducing bacteria growing on toluene.

J Flyvbjerg 1, C Jørgensen 1, E Arvin 1, B K Jensen 1, S K Olsen 1
PMCID: PMC182270  PMID: 8357260

Abstract

A mixed culture of nitrate-reducing bacteria degraded o-cresol in the presence of toulene as a primary growth substrate. No degradation of o-cresol was observed in the absence of toluene or when the culture grew on p-cresol and 2,4-dimethylphenol. In batch cultures, the degradation of o-cresol started after toluene was degraded to below 0.5 to 1.0 mg/liter but continued only for about 3 to 5 days after the depletion of toluene since the culture had a limited capacity for o-cresol degradation once toluene was depleted. The total amount of o-cresol degraded was proportional to the amount of toluene metabolized, with an average yield of 0.47 mg of o-cresol degraded per mg of toluene metabolized. Experiments with [ring-U-14C]o-cresol indicated that about 73% of the carbon from degraded o-cresol was mineralized to CO2 and about 23% was assimilated into biomass after the transient accumulation of unidentified water-soluble intermediates. A mathematical model based on a simplified Monod equation is used to describe the kinetics of o-cresol degradation. In this model, the biomass activity toward o-cresol is assumed to decay according to first-order kinetics once toluene is depleted. On the basis of nonlinear regression of the data, the maximum specific rate of o-cresol degradation was estimated to be 0.4 mg of o-cresol per mg of biomass protein per h, and the first-order decay constant for o-cresol-degrading biomass activity was estimated to be 0.15 h-1.(ABSTRACT TRUNCATED AT 250 WORDS)

Full text

PDF
2286

Selected References

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

  1. Alvarez P. J., Vogel T. M. Substrate interactions of benzene, toluene, and para-xylene during microbial degradation by pure cultures and mixed culture aquifer slurries. Appl Environ Microbiol. 1991 Oct;57(10):2981–2985. doi: 10.1128/aem.57.10.2981-2985.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arvin E., Jensen B. K., Gundersen A. T. Substrate interactions during aerobic biodegradation of benzene. Appl Environ Microbiol. 1989 Dec;55(12):3221–3225. doi: 10.1128/aem.55.12.3221-3225.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bisaillon J. G., Lépine F., Beaudet R., Sylvestre M. Carboxylation of o-cresol by an anaerobic consortium under methanogenic conditions. Appl Environ Microbiol. 1991 Aug;57(8):2131–2134. doi: 10.1128/aem.57.8.2131-2134.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bossert I. D., Young L. Y. Anaerobic oxidation of p-cresol by a denitrifying bacterium. Appl Environ Microbiol. 1986 Nov;52(5):1117–1122. doi: 10.1128/aem.52.5.1117-1122.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. 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]
  6. Evans P. J., Mang D. T., Kim K. S., Young L. Y. Anaerobic degradation of toluene by a denitrifying bacterium. Appl Environ Microbiol. 1991 Apr;57(4):1139–1145. doi: 10.1128/aem.57.4.1139-1145.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Evans P. J., Mang D. T., Young L. Y. Degradation of toluene and m-xylene and transformation of o-xylene by denitrifying enrichment cultures. Appl Environ Microbiol. 1991 Feb;57(2):450–454. doi: 10.1128/aem.57.2.450-454.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gälli R., McCarty P. L. Biotransformation of 1,1,1-trichloroethane, trichloromethane, and tetrachloromethane by a Clostridium sp. Appl Environ Microbiol. 1989 Apr;55(4):837–844. doi: 10.1128/aem.55.4.837-844.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kuhn E. P., Zeyer J., Eicher P., Schwarzenbach R. P. Anaerobic degradation of alkylated benzenes in denitrifying laboratory aquifer columns. Appl Environ Microbiol. 1988 Feb;54(2):490–496. doi: 10.1128/aem.54.2.490-496.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Platen H., Schink B. Anaerobic degradation of acetone and higher ketones via carboxylation by newly isolated denitrifying bacteria. J Gen Microbiol. 1989 Apr;135(4):883–891. doi: 10.1099/00221287-135-4-883. [DOI] [PubMed] [Google Scholar]
  11. Rudolphi A., Tschech A., Fuchs G. Anaerobic degradation of cresols by denitrifying bacteria. Arch Microbiol. 1991;155(3):238–248. doi: 10.1007/BF00252207. [DOI] [PubMed] [Google Scholar]
  12. Schocher R. J., Seyfried B., Vazquez F., Zeyer J. Anaerobic degradation of toluene by pure cultures of denitrifying bacteria. Arch Microbiol. 1991;157(1):7–12. doi: 10.1007/BF00245327. [DOI] [PubMed] [Google Scholar]
  13. Smolenski W. J., Suflita J. M. Biodegradation of cresol isomers in anoxic aquifers. Appl Environ Microbiol. 1987 Apr;53(4):710–716. doi: 10.1128/aem.53.4.710-716.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Tschech A., Fuchs G. Anaerobic degradation of phenol by pure cultures of newly isolated denitrifying pseudomonads. Arch Microbiol. 1987 Sep;148(3):213–217. doi: 10.1007/BF00414814. [DOI] [PubMed] [Google Scholar]
  15. Zeyer J., Kuhn E. P., Schwarzenbach R. P. Rapid microbial mineralization of toluene and 1,3-dimethylbenzene in the absence of molecular oxygen. Appl Environ Microbiol. 1986 Oct;52(4):944–947. doi: 10.1128/aem.52.4.944-947.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES