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PMID: 16347202 Published · ppublish English Journal Article

Metabolism of reduced methylated sulfur compounds in anaerobic sediments and by a pure culture of an estuarine methanogen.

Applied and environmental microbiology ·Vol. 52 ·No. 5 ·1986-11-00 ·Pages 1037-45

Kiene RP, Oremland RS, Catena A, Miller LG, Capone DG

Abstract

Addition of dimethylsulfide (DMS), dimethyldisulfide (DMDS), or methane thiol (MSH) to a diversity of anoxic aquatic sediments (e.g., fresh water, estuarine, alkaline/hypersaline) stimulated methane production. The yield of methane recovered from DMS was often 52 to 63%, although high concentrations of DMS (as well as MSH and DMDS) inhibited methanogenesis in some types of sediments. Production of methane from these reduced methylated sulfur compounds was blocked by 2-bromoethanesulfonic acid. Sulfate did not influence the metabolism of millimolar levels of DMS, DMDS, or MSH added to sediments. However, when DMS was added at approximately 2-muM levels as [C]DMS, metabolism by sediments resulted in a CH(4)/CO(2) ratio of only 0.06. Addition of molybdate increased the ratio to 1.8, while 2-bromoethanesulfonic acid decreased it to 0, but did not block CO(2) production. These results indicate the methanogens and sulfate reducers compete for DMS when it is present at low concentrations; however, at high concentrations, DMS is a "noncompetitive" substrate for methanogens. Metabolism of DMS by sediments resulted in the appearance of MSH as a transient intermediate. A pure culture of an obligately methylotrophic estuarine methanogen was isolated which was capable of growth on DMS. Metabolism of DMS by the culture also resulted in the transient appearance of MSH, but the organism could grow on neither MSH nor DMDS. The culture metabolized [C]-DMS to yield a CH(4)/CO(2) ratio of approximately 2.8. Reduced methylated sulfur compounds represent a new class of substrates for methanogens and may be potential precursors of methane in a variety of aquatic habitats.

Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kiene R P
Marine Sciences Research Center, State University of New York, Stony Brook, New York 11794; Water Resources Division, U.S. Geological Survey, Menlo Park, California 94025; and Department of Biological Sciences, San Francisco State University, San Francisco, California 94132.
Oremland R S
Catena A
Miller L G
Capone D G
References (16)
16 references, click to expand
  1. Preparation of coenzyme M analogues and their activity in the methyl coenzyme M reductase system of Methanobacterium thermoautotrophicum.
    Biochemistry. 1978 Jun 13;17(12):2374-7 PMID: 98178
  2. Utilization of trimethylamine and other N-methyl compounds for growth and methane formation by Methanosarcina barkeri.
    Proc Natl Acad Sci U S A. 1979 Jan;76(1):494-8 PMID: 284366
  3. Methanococcus vannielii: culture and effects of selenium and tungsten on growth.
    J Bacteriol. 1977 Jun;130(3):1404-6 PMID: 324989
  4. Use of nuclepore filters for counting bacteria by fluorescence microscopy.
    Appl Environ Microbiol. 1977 May;33(5):1225-8 PMID: 327932
  5. Methanogens: reevaluation of a unique biological group.
    Microbiol Rev. 1979 Jun;43(2):260-96 PMID: 390357
  6. Production of volatile sulfur compounds during the decomposition of algal mats.
    Appl Environ Microbiol. 1977 Dec;34(6):859-60 PMID: 413485
  7. The evaluation of media used to enumerate sulphate reducing bacteria.
    J Appl Bacteriol. 1970 Sep;33(3):543-52 PMID: 4923562
  8. Tentative identification of methanogenic bacteria by fluorescence microscopy.
    Appl Environ Microbiol. 1977 Mar;33(3):713-7 PMID: 16345230
  9. Methane, carbon dioxide, and hydrogen sulfide production from the terminal methiol group of methionine by anaerobic lake sediments.
    Appl Environ Microbiol. 1978 Feb;35(2):344-52 PMID: 16345275
  10. Anaerobic oxidation of acetylene by estuarine sediments and enrichment cultures.
    Appl Environ Microbiol. 1981 Feb;41(2):396-403 PMID: 16345714
  11. Microbial formation of ethane in anoxic estuarine sediments.
    Appl Environ Microbiol. 1981 Jul;42(1):122-9 PMID: 16345805
  12. Methanogenesis in big soda lake, nevada: an alkaline, moderately hypersaline desert lake.
    Appl Environ Microbiol. 1982 Feb;43(2):462-8 PMID: 16345952
  13. Methanogenesis and sulfate reduction: competitive and noncompetitive substrates in estuarine sediments.
    Appl Environ Microbiol. 1982 Dec;44(6):1270-6 PMID: 16346144
  14. Isolation and Characterization of a Methylotrophic Marine Methanogen, Methanococcoides methylutens gen. nov., sp. nov.
    Appl Environ Microbiol. 1983 Feb;45(2):684-90 PMID: 16346215
  15. Hydrogen metabolism by decomposing cyanobacterial aggregates in big soda lake, nevada.
    Appl Environ Microbiol. 1983 May;45(5):1519-25 PMID: 16346289
  16. Dimethyl sulfide in the surface ocean and the marine atmosphere: a global view.
    Science. 1983 Aug 19;221(4612):744-7 PMID: 17829533
Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
1986-11-00
Pages
1037-45
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC239170
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