Skip to main content
PMC home page
Gut logoLink to Gut
. 1993 Apr;34(4):437–439. doi: 10.1136/gut.34.4.437

Sulphate reducing bacteria and hydrogen metabolism in the human large intestine.

G R Gibson 1, G T Macfarlane 1, J H Cummings 1
PMCID: PMC1374298  PMID: 8491386

Full text

PDF
438

Selected References

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

  1. Abram J. W., Nedwell D. B. Hydrogen as a substrate for methanogenesis and sulphate reduction in anaerobic saltmarsh sediment. Arch Microbiol. 1978 Apr 27;117(1):93–97. doi: 10.1007/BF00689357. [DOI] [PubMed] [Google Scholar]
  2. Abram J. W., Nedwell D. B. Inhibition of methanogenesis by sulphate reducing bacteria competing for transferred hydrogen. Arch Microbiol. 1978 Apr 27;117(1):89–92. doi: 10.1007/BF00689356. [DOI] [PubMed] [Google Scholar]
  3. Anderson I. H., Levine A. S., Levitt M. D. Incomplete absorption of the carbohydrate in all-purpose wheat flour. N Engl J Med. 1981 Apr 9;304(15):891–892. doi: 10.1056/NEJM198104093041507. [DOI] [PubMed] [Google Scholar]
  4. Bond J. H., Jr, Engel R. R., Levitt M. D. Factors influencing pulmonary methane excretion in man. An indirect method of studying the in situ metabolism of the methane-producing colonic bacteria. J Exp Med. 1971 Mar 1;133(3):572–588. doi: 10.1084/jem.133.3.572. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bond J. H., Jr, Levitt M. D. Use of pulmonary hydrogen (H 2 ) measurements to quantitate carbohydrate absorption. Study of partially gastrectomized patients. J Clin Invest. 1972 May;51(5):1219–1225. doi: 10.1172/JCI106916. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Breznak J. A., Switzer J. M. Acetate Synthesis from H(2) plus CO(2) by Termite Gut Microbes. Appl Environ Microbiol. 1986 Oct;52(4):623–630. doi: 10.1128/aem.52.4.623-630.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cummings J. H., Macfarlane G. T. The control and consequences of bacterial fermentation in the human colon. J Appl Bacteriol. 1991 Jun;70(6):443–459. doi: 10.1111/j.1365-2672.1991.tb02739.x. [DOI] [PubMed] [Google Scholar]
  8. Filipe M. I. Mucins in the human gastrointestinal epithelium: a review. Invest Cell Pathol. 1979 Jul-Sep;2(3):195–216. [PubMed] [Google Scholar]
  9. Florin T., Neale G., Gibson G. R., Christl S. U., Cummings J. H. Metabolism of dietary sulphate: absorption and excretion in humans. Gut. 1991 Jul;32(7):766–773. doi: 10.1136/gut.32.7.766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gibson G. R., Cummings J. H., Macfarlane G. T., Allison C., Segal I., Vorster H. H., Walker A. R. Alternative pathways for hydrogen disposal during fermentation in the human colon. Gut. 1990 Jun;31(6):679–683. doi: 10.1136/gut.31.6.679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gibson G. R., Cummings J. H., Macfarlane G. T. Competition for hydrogen between sulphate-reducing bacteria and methanogenic bacteria from the human large intestine. J Appl Bacteriol. 1988 Sep;65(3):241–247. doi: 10.1111/j.1365-2672.1988.tb01891.x. [DOI] [PubMed] [Google Scholar]
  12. Gibson G. R., Cummings J. H., Macfarlane G. T. Use of a three-stage continuous culture system to study the effect of mucin on dissimilatory sulfate reduction and methanogenesis by mixed populations of human gut bacteria. Appl Environ Microbiol. 1988 Nov;54(11):2750–2755. doi: 10.1128/aem.54.11.2750-2755.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gibson G. R., Macfarlane G. T., Cummings J. H. Occurrence of sulphate-reducing bacteria in human faeces and the relationship of dissimilatory sulphate reduction to methanogenesis in the large gut. J Appl Bacteriol. 1988 Aug;65(2):103–111. doi: 10.1111/j.1365-2672.1988.tb01498.x. [DOI] [PubMed] [Google Scholar]
  14. Gibson G. R. Physiology and ecology of the sulphate-reducing bacteria. J Appl Bacteriol. 1990 Dec;69(6):769–797. doi: 10.1111/j.1365-2672.1990.tb01575.x. [DOI] [PubMed] [Google Scholar]
  15. Ishioka T., Kuwabara N., Oohashi Y., Wakabayashi K. Induction of colorectal tumors in rats by sulfated polysaccharides. Crit Rev Toxicol. 1987;17(3):215–244. doi: 10.3109/10408448709071209. [DOI] [PubMed] [Google Scholar]
  16. JENNINGS M. A., FLOREY H. W. Autoradiographic observations on the mucous cells of the stomach and intestine. Q J Exp Physiol Cogn Med Sci. 1956 Apr;41(2):131–152. doi: 10.1113/expphysiol.1956.sp001171. [DOI] [PubMed] [Google Scholar]
  17. King G. M., Wiebe W. J. Tracer analysis of methanogenesis in salt marsh soils. Appl Environ Microbiol. 1980 Apr;39(4):877–881. doi: 10.1128/aem.39.4.877-881.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lajoie S. F., Bank S., Miller T. L., Wolin M. J. Acetate production from hydrogen and [13C]carbon dioxide by the microflora of human feces. Appl Environ Microbiol. 1988 Nov;54(11):2723–2727. doi: 10.1128/aem.54.11.2723-2727.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Levitt M. D., Hirsh P., Fetzer C. A., Sheahan M., Levine A. S. H2 excretion after ingestion of complex carbohydrates. Gastroenterology. 1987 Feb;92(2):383–389. doi: 10.1016/0016-5085(87)90132-6. [DOI] [PubMed] [Google Scholar]
  20. Ljungdahl L. G. The autotrophic pathway of acetate synthesis in acetogenic bacteria. Annu Rev Microbiol. 1986;40:415–450. doi: 10.1146/annurev.mi.40.100186.002215. [DOI] [PubMed] [Google Scholar]
  21. 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]
  22. 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]
  23. Macfarlane G. T., Gibson G. R. Formation of glycoprotein degrading enzymes by Bacteroides fragilis. FEMS Microbiol Lett. 1991 Jan 15;61(2-3):289–293. doi: 10.1016/0378-1097(91)90567-t. [DOI] [PubMed] [Google Scholar]
  24. Macfarlane G. T., Hay S., Gibson G. R. Influence of mucin on glycosidase, protease and arylamidase activities of human gut bacteria grown in a 3-stage continuous culture system. J Appl Bacteriol. 1989 May;66(5):407–417. doi: 10.1111/j.1365-2672.1989.tb05110.x. [DOI] [PubMed] [Google Scholar]
  25. Martens C. S., Berner R. A. Methane production in the interstitial waters of sulfate-depleted marine sediments. Science. 1974 Sep 27;185(4157):1167–1169. doi: 10.1126/science.185.4157.1167. [DOI] [PubMed] [Google Scholar]
  26. 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]
  27. Mountfort D. O., Asher R. A. Role of sulfate reduction versus methanogenesis in terminal carbon flow in polluted intertidal sediment of waimea inlet, nelson, new zealand. Appl Environ Microbiol. 1981 Aug;42(2):252–258. doi: 10.1128/aem.42.2.252-258.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Oremland R. S., Polcin S. Methanogenesis and sulfate reduction: competitive and noncompetitive substrates in estuarine sediments. Appl Environ Microbiol. 1982 Dec;44(6):1270–1276. doi: 10.1128/aem.44.6.1270-1276.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Roberton A. M., Stanley R. A. In vitro utilization of mucin by Bacteroides fragilis. Appl Environ Microbiol. 1982 Feb;43(2):325–330. doi: 10.1128/aem.43.2.325-330.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Roediger W. E., Nance S. Selective reduction of fatty acid oxidation in colonocytes: correlation with ulcerative colitis. Lipids. 1990 Oct;25(10):646–652. doi: 10.1007/BF02536016. [DOI] [PubMed] [Google Scholar]
  31. Salyers A. A., O'Brien M. Cellular location of enzymes involved in chondroitin sulfate breakdown by Bacteroides thetaiotaomicron. J Bacteriol. 1980 Aug;143(2):772–780. doi: 10.1128/jb.143.2.772-780.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Strocchi A., Furne J. K., Ellis C. J., Levitt M. D. Competition for hydrogen by human faecal bacteria: evidence for the predominance of methane producing bacteria. Gut. 1991 Dec;32(12):1498–1501. doi: 10.1136/gut.32.12.1498. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Thauer R. K., Jungermann K., Decker K. Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev. 1977 Mar;41(1):100–180. doi: 10.1128/br.41.1.100-180.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Vercellotti J. R., Salyers A. A., Bullard W. S., Wilkins D. Breakdown of mucin and plant polysaccharides in the human colon. Can J Biochem. 1977 Nov;55(11):1190–1196. doi: 10.1139/o77-178. [DOI] [PubMed] [Google Scholar]
  35. 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]

Articles from Gut are provided here courtesy of BMJ Publishing Group

RESOURCES