Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1984 Feb;47(2):403–408. doi: 10.1128/aem.47.2.403-408.1984

Kinetics of Sulfate and Acetate Uptake by Desulfobacter postgatei

Kjeld Ingvorsen 1,†,*, Alexander J B Zehnder 1,, Bo B Jørgensen 1
PMCID: PMC239682  PMID: 16346478

Abstract

The kinetics of sulfate and acetate uptake was studied in the sulfate-reducing bacterium Desulfobacter postgatei (DSM 2034). Kinetic parameters (Km and Vmax) were estimated from substrate consumption curves by resting cell suspensions with [35S]sulfate and [14C]acetate. Both sulfate and acetate consumption followed Michaelis-Menten saturation kinetics. The half-saturation constant (Km) for acetate uptake was 70 μM with cells from either long-term sulfate- or long-term acetate-limited chemostat cultures. The average Km value for sulfate uptake by D. postgatei was about 200 μM. Km values for sulfate uptake did not differ significantly when determined with cells derived either from batch cultures or sulfate- or acetate-limited chemostat cultures. Acetate consumption was observed at acetate concentrations of ≤1 μM, whereas sulfate uptake usually ceased at 5 to 20 μM. The results show that D. postgatei is not freely permeable to sulfate ions and further indicate that sulfate uptake is an energy-requiring process.

Full text

PDF
403

Selected References

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

  1. 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]
  2. Bryant M. P., Campbell L. L., Reddy C. A., Crabill M. R. Growth of desulfovibrio in lactate or ethanol media low in sulfate in association with H2-utilizing methanogenic bacteria. Appl Environ Microbiol. 1977 May;33(5):1162–1169. doi: 10.1128/aem.33.5.1162-1169.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. FURUSAKA C. Sulphate transport and metabolism by Desulphovibrio desulphuricans. Nature. 1961 Nov 4;192:427–429. doi: 10.1038/192427a0. [DOI] [PubMed] [Google Scholar]
  4. HERBERT D., ELSWORTH R., TELLING R. C. The continuous culture of bacteria; a theoretical and experimental study. J Gen Microbiol. 1956 Jul;14(3):601–622. doi: 10.1099/00221287-14-3-601. [DOI] [PubMed] [Google Scholar]
  5. Harder W., Dijkhuizen L. Strategies of mixed substrate utilization in microorganisms. Philos Trans R Soc Lond B Biol Sci. 1982 Jun 11;297(1088):459–480. doi: 10.1098/rstb.1982.0055. [DOI] [PubMed] [Google Scholar]
  6. Ingvorsen K., Zeikus J. G., Brock T. D. Dynamics of bacterial sulfate reduction in a eutrophic lake. Appl Environ Microbiol. 1981 Dec;42(6):1029–1036. doi: 10.1128/aem.42.6.1029-1036.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Koch A. L. The adaptive responses of Escherichia coli to a feast and famine existence. Adv Microb Physiol. 1971;6:147–217. doi: 10.1016/s0065-2911(08)60069-7. [DOI] [PubMed] [Google Scholar]
  8. Koch A. L., Wang C. H. How close to the theoretical diffusion limit do bacterial uptake systems function? Arch Microbiol. 1982 Feb;131(1):36–42. doi: 10.1007/BF00451496. [DOI] [PubMed] [Google Scholar]
  9. LITTLEWOOD D., POSTGATE J. R. On the osmotic behaviour of Desulphovibrio desulphuricans. J Gen Microbiol. 1957 Jun;16(3):596–603. doi: 10.1099/00221287-16-3-596. [DOI] [PubMed] [Google Scholar]
  10. Laanbroek H. J., Pfennig N. Oxidation of short-chain fatty acids by sulfate-reducing bacteria in freshwater and in marine sediments. Arch Microbiol. 1981 Jan;128(3):330–335. doi: 10.1007/BF00422540. [DOI] [PubMed] [Google Scholar]
  11. Lovley D. R., Dwyer D. F., Klug M. J. Kinetic analysis of competition between sulfate reducers and methanogens for hydrogen in sediments. Appl Environ Microbiol. 1982 Jun;43(6):1373–1379. doi: 10.1128/aem.43.6.1373-1379.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Lovley D. R., Klug M. J. Intermediary metabolism of organic matter in the sediments of a eutrophic lake. Appl Environ Microbiol. 1982 Mar;43(3):552–560. doi: 10.1128/aem.43.3.552-560.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Lovley D. R., Klug M. J. Sulfate reducers can outcompete methanogens at freshwater sulfate concentrations. Appl Environ Microbiol. 1983 Jan;45(1):187–192. doi: 10.1128/aem.45.1.187-192.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Macy J. M., Snellen J. E., Hungate R. E. Use of syringe methods for anaerobiosis. Am J Clin Nutr. 1972 Dec;25(12):1318–1323. doi: 10.1093/ajcn/25.12.1318. [DOI] [PubMed] [Google Scholar]
  15. Mountfort D. O., Asher R. A., Mays E. L., Tiedje J. M. Carbon and electron flow in mud and sandflat intertidal sediments at delaware inlet, nelson, new zealand. Appl Environ Microbiol. 1980 Apr;39(4):686–694. doi: 10.1128/aem.39.4.686-694.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Peck H. D., Jr, LeGall J. Biochemistry of dissimilatory sulphate reduction. Philos Trans R Soc Lond B Biol Sci. 1982 Sep 13;298(1093):443–466. doi: 10.1098/rstb.1982.0091. [DOI] [PubMed] [Google Scholar]
  17. Pfennig N., Widdel F. The bacteria of the sulphur cycle. Philos Trans R Soc Lond B Biol Sci. 1982 Sep 13;298(1093):433–441. doi: 10.1098/rstb.1982.0090. [DOI] [PubMed] [Google Scholar]
  18. Smith M. R., Mah R. A. Growth and methanogenesis by Methanosarcina strain 227 on acetate and methanol. Appl Environ Microbiol. 1978 Dec;36(6):870–879. doi: 10.1128/aem.36.6.870-879.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Smith R. L., Klug M. J. Reduction of sulfur compounds in the sediments of a eutrophic lake basin. Appl Environ Microbiol. 1981 May;41(5):1230–1237. doi: 10.1128/aem.41.5.1230-1237.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Sørensen J., Christensen D., Jørgensen B. B. Volatile Fatty acids and hydrogen as substrates for sulfate-reducing bacteria in anaerobic marine sediment. Appl Environ Microbiol. 1981 Jul;42(1):5–11. doi: 10.1128/aem.42.1.5-11.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Thauer R. K. Dissimilatory sulphate reduction with acetate as electron donor. Philos Trans R Soc Lond B Biol Sci. 1982 Sep 13;298(1093):467–471. doi: 10.1098/rstb.1982.0092. [DOI] [PubMed] [Google Scholar]
  22. 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]
  23. Widdel F., Pfennig N. A new anaerobic, sporing, acetate-oxidizing, sulfate-reducing bacterium, Desulfotomaculum (emend.) acetoxidans. Arch Microbiol. 1977 Feb 4;112(1):119–122. doi: 10.1007/BF00446665. [DOI] [PubMed] [Google Scholar]
  24. Widdel F., Pfennig N. Studies on dissimilatory sulfate-reducing bacteria that decompose fatty acids. I. Isolation of new sulfate-reducing bacteria enriched with acetate from saline environments. Description of Desulfobacter postgatei gen. nov., sp. nov. Arch Microbiol. 1981 Jul;129(5):395–400. doi: 10.1007/BF00406470. [DOI] [PubMed] [Google Scholar]
  25. Winfrey M. R., Zeikus J. G. Anaerobic metabolism of immediate methane precursors in Lake Mendota. Appl Environ Microbiol. 1979 Feb;37(2):244–253. doi: 10.1128/aem.37.2.244-253.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Winfrey M. R., Zeikus J. G. Effect of sulfate on carbon and electron flow during microbial methanogenesis in freshwater sediments. Appl Environ Microbiol. 1977 Feb;33(2):275–281. doi: 10.1128/aem.33.2.275-281.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Zehnder A. J., Huser B. A., Brock T. D., Wuhrmann K. Characterization of an acetate-decarboxylating, non-hydrogen-oxidizing methane bacterium. Arch Microbiol. 1980 Jan;124(1):1–11. doi: 10.1007/BF00407022. [DOI] [PubMed] [Google Scholar]

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

RESOURCES