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Chemical transformation of xenobiotics by the human gut microbiota

Journal

SCIENCE
Volume 356, Issue 6344, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aag2770

Keywords

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Funding

  1. Smith Family Award for Biomedical Research
  2. Damon Runyon-Rachleff Innovation Award
  3. George W. Merck Fellowship
  4. David and Lucille Packard Foundation
  5. Howard Hughes Medical Institute-Gates Faculty Scholar Award [OPP1158186]
  6. Massachusetts Institute of Technology Center for Microbiome Informatics and Therapeutics
  7. Sloan Research Fellowship
  8. Blavatnik Biomedical Accelerator Award
  9. Takeda
  10. Defense Advanced Research Projects Agency [HR0011-16-2-0013]
  11. NIH [CA208834, 5T32GM007598]
  12. NSF [MCB-1650086, DGE1144152]
  13. Bill and Melinda Gates Foundation [OPP1158186] Funding Source: Bill and Melinda Gates Foundation

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The human gut microbiota makes key contributions to the metabolism of ingested compounds (xenobiotics), transforming hundreds of dietary components, industrial chemicals, and pharmaceuticals into metabolites with altered activities, toxicities, and lifetimes within the body. The chemistry of gut microbial xenobiotic metabolism is often distinct from that of host enzymes. Despite their important consequences for human biology, the gut microbes, genes, and enzymes involved in xenobiotic metabolism are poorly understood. Linking these microbial transformations to enzymes and elucidating their biological effects is undoubtedly challenging. However, recent studies demonstrate that integrating traditional and emerging technologies can enable progress toward this goal. Ultimately, a molecular understanding of gut microbial xenobiotic metabolism will guide personalized medicine and nutrition, inform toxicology risk assessment, and improve drug discovery and development.

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