Abstract
In environments with temperatures above 60°C, thermophilic prokaryotes are the only metabolically active life-forms. By using the 35SO42- tracer technique, we studied the activity of sulfate-reducing microorganisms (SRM) in hot sediment from a hydrothermal vent site in the northern part of freshwater Lake Tanganyika (East Africa). Incubation of slurry samples at 8 to 90°C demonstrated meso- and thermophilic sulfate reduction with optimum temperatures of 34 to 45°C and 56 to 65°C, respectively, and with an upper temperature limit of 80°C. Sulfate reduction was stimulated at all temperatures by the addition of short-chain fatty acids and benzoate or complex substrates (yeast extract and peptone). A time course experiment showed that linear thermophilic sulfate consumption occurred after a lag phase (12 h) and indicated the presence of a large population of SRM in the hydrothermal sediment. Thermophilic sulfate reduction had a pH optimum of about 7 and was completely inhibited at pH 8.8 to 9.2. SRM could be enriched from hydrothermal chimney and sediment samples at 60 and 75°C. In lactate-grown enrichments, sulfide production occurred at up to 70 and 75°C, with optima at 63 and 71°C, respectively. Several sporulating thermophilic enrichments were morphologically similar to Desulfotomaculum spp. Dissimilatory sulfate reduction in the studied hydrothermal area of Lake Tanganyika apparently has an upper temperature limit of 80°C.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brock T. D. Life at high temperatures. Science. 1985 Oct 11;230(4722):132–138. doi: 10.1126/science.230.4722.132. [DOI] [PubMed] [Google Scholar]
- Henry E. A., Devereux R., Maki J. S., Gilmour C. C., Woese C. R., Mandelco L., Schauder R., Remsen C. C., Mitchell R. Characterization of a new thermophilic sulfate-reducing bacterium Thermodesulfovibrio yellowstonii, gen. nov. and sp. nov.: its phylogenetic relationship to Thermodesulfobacterium commune and their origins deep within the bacterial domain. Arch Microbiol. 1994 Jan;161(1):62–69. [PubMed] [Google Scholar]
- Jannasch H. W., Mottl M. J. Geomicrobiology of deep-sea hydrothermal vents. Science. 1985 Aug 23;229(4715):717–725. doi: 10.1126/science.229.4715.717. [DOI] [PubMed] [Google Scholar]
- Jannasch H. W., Wirsen C. O., Molyneaux S. J., Langworthy T. A. Comparative Physiological Studies on Hyperthermophilic Archaea Isolated from Deep-Sea Hot Vents with Emphasis on Pyrococcus Strain GB-D. Appl Environ Microbiol. 1992 Nov;58(11):3472–3481. doi: 10.1128/aem.58.11.3472-3481.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jørgensen B. B., Isaksen M. F., Jannasch H. W. Bacterial Sulfate Reduction Above 100{degrees}C in Deep-Sea Hydrothermal Vent Sediments. Science. 1992 Dec 11;258(5089):1756–1757. doi: 10.1126/science.258.5089.1756. [DOI] [PubMed] [Google Scholar]
- Rosnes J. T., Torsvik T., Lien T. Spore-forming thermophilic sulfate-reducing bacteria isolated from north sea oil field waters. Appl Environ Microbiol. 1991 Aug;57(8):2302–2307. doi: 10.1128/aem.57.8.2302-2307.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- 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]
- Wiegel J., Ljungdahl L. G., Rawson J. R. Isolation from soil and properties of the extreme thermophile Clostridium thermohydrosulfuricum. J Bacteriol. 1979 Sep;139(3):800–810. doi: 10.1128/jb.139.3.800-810.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]