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Metabolic Fingerprint of Dimethyl Sulfone (DMSO2) in Microbial–Mammalian Co-metabolism

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Department of Nutrition, Department of Food Science and Technology, One Shields Avenue, University of California, Davis, Davis, California 95616, United States
*Telephone: 530-752-6804. Fax: 530-752-8966. E-mail: [email protected]
Cite this: J. Proteome Res. 2014, 13, 12, 5281–5292
Publication Date (Web):September 23, 2014
https://doi.org/10.1021/pr500629t
Copyright © 2014 American Chemical Society

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    Abstract

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    There is growing awareness that intestinal microbiota alters the energy harvesting capacity of the host and regulates metabolism. It has been postulated that intestinal microbiota are able to degrade unabsorbed dietary components and transform xenobiotic compounds. The resulting microbial metabolites derived from the gastrointestinal tract can potentially enter the circulation system, which, in turn, affects host metabolism. Yet, the metabolic capacity of intestinal microbiota and its interaction with mammalian metabolism remains largely unexplored. Here, we review a metabolic pathway that integrates the microbial catabolism of methionine with mammalian metabolism of methanethiol (MT), dimethyl sulfide (DMS), and dimethyl sulfoxide (DMSO), which together provide evidence that supports the microbial origin of dimethyl sulfone (DMSO2) in the human metabolome. Understanding the pathway of DMSO2 co-metabolism expends our knowledge of microbial-derived metabolites and motivates future metabolomics-based studies on ascertaining the metabolic consequences of intestinal microbiota on human health, including detoxification processes and sulfur xenobiotic metabolism.

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    Elimination and excretion patterns of dimethyl sulfoxide (DMSO), dimethyl sulfone (DMSO2), and dimethyl sulfide (DMS) after administration of DMSO. This material is available free of charge via the Internet at http://pubs.acs.org.

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