Utilization of trimethylamine and other N-methyl compounds for growth and methane formation by Methanosarcina barkeri
- PMID: 284366
- PMCID: PMC382968
- DOI: 10.1073/pnas.76.1.494
Utilization of trimethylamine and other N-methyl compounds for growth and methane formation by Methanosarcina barkeri
Abstract
A number of N-methyl compounds, including several methylamines, creatine, sarcosine, choline, and betaine, were readily fermented by enrichment cultures yielding methane as a major product. Methylamine, dimethylamine, trimethylamine, and ethyldimethylamine were fermented by pure cultures of Methanosarcina barkeri; except for ethyldimethylamine, these amines are considered important substrates of this methanogenic microorganism. Creatine, sarcosine, choline, and betaine were fermented to methane only by mixed cultures. During growth of M. barkeri on methyl-, dimethyl-, or trimethylamine, methanol was not excreted into the medium. The fermentation of trimethylamine gave rise to an intermediary accumulation of methyl- and dimethylamine in the medium. An accumulation of methylamine during the fermentation of dimethylamine was not observed. Methane and ammonia were produced from the three methylamines by M. barkeri in amounts expected on the basis of the appropriate fermentation equations. The growth yield was 5.8 mg of cells (dry weight) per mmol of methane and was not dependent on the kind of methyl compound used as substrate.
Similar articles
-
Formation of trideuteromethane from deuterated trimethylamine or methylamine by Methanosarcina barkeri.J Bacteriol. 1981 Oct;148(1):371-3. doi: 10.1128/jb.148.1.371-373.1981. J Bacteriol. 1981. PMID: 7287629 Free PMC article.
-
Methyl-coenzyme M, an intermediate in methanogenic dissimilation of C1 compounds by Methanosarcina barkeri.J Bacteriol. 1980 Feb;141(2):728-34. doi: 10.1128/jb.141.2.728-734.1980. J Bacteriol. 1980. PMID: 6444945 Free PMC article.
-
Specific roles of methylcobamide:coenzyme M methyltransferase isozymes in metabolism of methanol and methylamines in Methanosarcina barkeri.J Biol Chem. 1996 Mar 1;271(9):5189-94. doi: 10.1074/jbc.271.9.5189. J Biol Chem. 1996. PMID: 8617801
-
Formation and breakdown of glycine betaine and trimethylamine in hypersaline environments.Antonie Van Leeuwenhoek. 1990 Nov;58(4):291-8. doi: 10.1007/BF00399342. Antonie Van Leeuwenhoek. 1990. PMID: 2082817 Review.
-
Metabolism of one-carbon compounds by chemotrophic anaerobes.Adv Microb Physiol. 1983;24:215-99. doi: 10.1016/s0065-2911(08)60387-2. Adv Microb Physiol. 1983. PMID: 6364727 Review. No abstract available.
Cited by
-
Molecular Basis of C-N Bond Cleavage by the Glycyl Radical Enzyme Choline Trimethylamine-Lyase.Cell Chem Biol. 2016 Oct 20;23(10):1206-1216. doi: 10.1016/j.chembiol.2016.07.020. Epub 2016 Sep 24. Cell Chem Biol. 2016. PMID: 27642068 Free PMC article.
-
Anaerobic growth of Methanosarcina acetivorans C2A on carbon monoxide: an unusual way of life for a methanogenic archaeon.Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16929-34. doi: 10.1073/pnas.0407486101. Epub 2004 Nov 18. Proc Natl Acad Sci U S A. 2004. PMID: 15550538 Free PMC article.
-
Metabolism of reduced methylated sulfur compounds in anaerobic sediments and by a pure culture of an estuarine methanogen.Appl Environ Microbiol. 1986 Nov;52(5):1037-45. doi: 10.1128/aem.52.5.1037-1045.1986. Appl Environ Microbiol. 1986. PMID: 16347202 Free PMC article.
-
Atmospheric amines are a crucial yet missing link in Earth's climate via airborne aerosol production.Commun Earth Environ. 2025;6(1):98. doi: 10.1038/s43247-025-02063-0. Epub 2025 Feb 10. Commun Earth Environ. 2025. PMID: 39944636 Free PMC article. Review.
-
Nitrous oxide inhibition of methanogenesis represents an underappreciated greenhouse gas emission feedback.ISME J. 2024 Jan 8;18(1):wrae027. doi: 10.1093/ismejo/wrae027. ISME J. 2024. PMID: 38447133 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Molecular Biology Databases