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Microbial liberation of N-methylserotonin from orange fiber in gnotobiotic mice and humans.
Han, Nathan D; Cheng, Jiye; Delannoy-Bruno, Omar; Webber, Daniel; Terrapon, Nicolas; Henrissat, Bernard; Rodionov, Dmitry A; Arzamasov, Aleksandr A; Osterman, Andrei L; Hayashi, David K; Meynier, Alexandra; Vinoy, Sophie; Desai, Chandani; Marion, Stacey; Barratt, Michael J; Heath, Andrew C; Gordon, Jeffrey I.
  • Han ND; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA.
  • Cheng J; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA.
  • Delannoy-Bruno O; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA.
  • Webber D; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Terrapon N; Architecture et Fonction des Macromolécules Biologiques, CNRS, Aix-Marseille University, 13288 Marseille, France.
  • Henrissat B; Architecture et Fonction des Macromolécules Biologiques, CNRS, Aix-Marseille University, 13288 Marseille, France; Department of Biotechnology and Biomedicine (DTU Bioengineering), Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.
  • Rodionov DA; Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
  • Arzamasov AA; Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
  • Osterman AL; Infectious and Inflammatory Disease Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.
  • Hayashi DK; Mondelez Global LLC, Chicago, IL 60607, USA.
  • Meynier A; Mondelez Global LLC, Chicago, IL 60607, USA.
  • Vinoy S; Mondelez Global LLC, Chicago, IL 60607, USA.
  • Desai C; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA.
  • Marion S; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Barratt MJ; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Heath AC; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Gordon JI; The Edison Family Center for Genome Sciences and Systems Biology, St. Louis, MO 63110, USA; Center for Gut Microbiome and Nutrition Research, St. Louis, MO 63110, USA. Electronic address: jgordon@wustl.edu.
Cell ; 185(14): 2495-2509.e11, 2022 07 07.
Article en En | MEDLINE | ID: mdl-35764090
ABSTRACT
Plant fibers in byproduct streams produced by non-harsh food processing methods represent biorepositories of diverse, naturally occurring, and physiologically active biomolecules. To demonstrate one approach for their characterization, mass spectrometry of intestinal contents from gnotobiotic mice, plus in vitro studies, revealed liberation of N-methylserotonin from orange fibers by human gut microbiota members including Bacteroides ovatus. Functional genomic analyses of B. ovatus strains grown under permissive and non-permissive N-methylserotonin "mining" conditions revealed polysaccharide utilization loci that target pectins whose expression correlate with strain-specific liberation of this compound. N-methylserotonin, orally administered to germ-free mice, reduced adiposity, altered liver glycogenesis, shortened gut transit time, and changed expression of genes that regulate circadian rhythm in the liver and colon. In human studies, dose-dependent, orange-fiber-specific fecal accumulation of N-methylserotonin positively correlated with levels of microbiome genes encoding enzymes that digest pectic glycans. Identifying this type of microbial mining activity has potential therapeutic implications.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Citrus sinensis / Microbioma Gastrointestinal Límite: Animals / Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Citrus sinensis / Microbioma Gastrointestinal Límite: Animals / Humans Idioma: En Año: 2022 Tipo del documento: Article