Abstract
One host (Rana catesbiana)-associated and two free-living mesophilic strains of bacteria with violet pigmentation and biochemical characteristics of Chromobacterium violaceum were isolated from freshwater habitats. Cells of each freshly isolated strain and of strain ATCC 12472 (the neotype strain) grew anaerobically with glucose as the sole carbon and energy source. The major fermentation products of cells grown in Trypticase soy broth (BBL Microbiology Systems, Cockeysville, Md.) supplemented with glucose included acetate, small amounts of propionate, lactate, and pyruvate. The final cell yield and culture growth rate of each strain cultured anaerobically in this medium increased approximately twofold with the addition of 2 mM NaNO3. Final growth yields increased in direct proportion to the quantity of added NaNO3 over the range of 0.5 to 5 mM. Each strain reduced NO3−, producing NO2−, NO, and N2O. NO2− accumulated transiently. With 2 mM NaNO3 in the medium, N2O made up 85 to 98% of the N product recovered with each strain. N-oxides were recovered in the same quantity and distribution whether 0.01 atm (ca. 1 kPa) of C2H2 (added to block N2O reduction) was present or not. Neither N2 production nor gas accumulation was detected during NO3− reduction by growing cells. Cell growth in media containing 0.5 to 5 mM NaNO2 in lieu of NaNO3 was delayed, and although N2O was produced by the end of growth, NO2− -containing media did not support growth to an extent greater than did medium lacking NO3− or NO2−. The data indicate that C. violaceum cells ferment glucose or denitrify, terminating denitrification with the production of N2O, and that NO2− reduction to N2O is not coupled to growth but may serve as a detoxification mechanism. No strain detectably fixed N2 (reduced C2H2).
Full text
PDF



Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- 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]
- Bazylinski D. A., Blakemore R. P. Denitrification and Assimilatory Nitrate Reduction in Aquaspirillum magnetotacticum. Appl Environ Microbiol. 1983 Nov;46(5):1118–1124. doi: 10.1128/aem.46.5.1118-1124.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bettelheim K. A., Gordon J. F., Taylor J. The detection of a strain of Chromobacterium lividum in the tissues of certain leaf-nodulated plants by the immunofluorescence technique. J Gen Microbiol. 1968 Dec;54(2):177–184. doi: 10.1099/00221287-54-2-177. [DOI] [PubMed] [Google Scholar]
- Blakemore R. P., Maratea D., Wolfe R. S. Isolation and pure culture of a freshwater magnetic spirillum in chemically defined medium. J Bacteriol. 1979 Nov;140(2):720–729. doi: 10.1128/jb.140.2.720-729.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bleakley B. H., Tiedje J. M. Nitrous oxide production by organisms other than nitrifiers or denitrifiers. Appl Environ Microbiol. 1982 Dec;44(6):1342–1348. doi: 10.1128/aem.44.6.1342-1348.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CORPE W. A. A study of the wide spread distribution of Chromobacterium species in soil by a simple technique. J Bacteriol. 1951 Oct;62(4):515–517. doi: 10.1128/jb.62.4.515-517.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CORPE W. A. The extracellular polysaccharide of gelatinous strains of Chromobacterium violaceum. Can J Microbiol. 1960 Apr;6:153–163. doi: 10.1139/m60-017. [DOI] [PubMed] [Google Scholar]
- ELTINGE E. T. Nitrate reduction in the genus Chromobacterium. Antonie Van Leeuwenhoek. 1956;22(2):139–144. doi: 10.1007/BF02538321. [DOI] [PubMed] [Google Scholar]
- Greenberg E. P., Becker G. E. Nitrous oxide as end product of denitrification by strains of fluorescent pseudomonads. Can J Microbiol. 1977 Jul;23(7):903–907. doi: 10.1139/m77-133. [DOI] [PubMed] [Google Scholar]
- Johnson W. M., DiSalvo A. F., Steuer R. R. Fatal Chromobacterium violaceum septicemia. Am J Clin Pathol. 1971 Sep;56(3):400–406. doi: 10.1093/ajcp/56.3.400. [DOI] [PubMed] [Google Scholar]
- Koburger J. A., May S. O. Isolation of Chromobacterium spp. from foods, soil, and water. Appl Environ Microbiol. 1982 Dec;44(6):1463–1465. doi: 10.1128/aem.44.6.1463-1465.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LEIFSON E. Morphological and physiological characteristics of the genus Chromobacterium. J Bacteriol. 1956 Apr;71(4):393–400. doi: 10.1128/jb.71.4.393-400.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Renner E. D., Becker G. E. Production of nitric oxide and nitrous oxide during denitrification by Corynebacterium nephridii. J Bacteriol. 1970 Mar;101(3):821–826. doi: 10.1128/jb.101.3.821-826.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SNEATH P. H. Cultural and biochemical characteristics of the genus Chromobacterium. J Gen Microbiol. 1956 Aug;15(1):70–98. doi: 10.1099/00221287-15-1-70. [DOI] [PubMed] [Google Scholar]
- Smith M. S. Dissimilatory Reduction of NO(2) to NH(4) and N(2)O by a Soil Citrobacter sp. Appl Environ Microbiol. 1982 Apr;43(4):854–860. doi: 10.1128/aem.43.4.854-860.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Van Gent-Ruijters M. L., DeVries W., Southamer A. H. Influence of nitrate on fermentation pattern, molar growth yields and synthesis of cytochrome b in Propionibacterium pentosaceum. J Gen Microbiol. 1975 May;88(1):36–48. doi: 10.1099/00221287-88-1-36. [DOI] [PubMed] [Google Scholar]
- Yoshinari T., Knowles R. Acetylene inhibition of nitrous oxide reduction by denitrifying bacteria. Biochem Biophys Res Commun. 1976 Apr 5;69(3):705–710. doi: 10.1016/0006-291x(76)90932-3. [DOI] [PubMed] [Google Scholar]
