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Microbial liberation of N-methylserotonin from orange fiber in gnotobiotic mice and humans
Author(s) -
Nathan D. Han,
Jiye Cheng,
Omar Delannoy-Bruno,
Daniel M. Webber,
Nicolas Terrapon,
Bernard Henrissat,
Dmitry A. Rodionov,
Aleksandr A. Arzamasov,
Andrei L. Osterman,
David K. Hayashi,
Alexandra Meynier,
Sophie Vinoy,
Chandni Desai,
Stacey Marion,
Michael J. Barratt,
Andrew C. Heath,
Jeffrey I. Gordon
Publication year - 2022
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2022.06.004
Subject(s) - biology , polysaccharide , bacteroides , microbiology and biotechnology , biochemistry , bacteria , genetics
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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