By the same authors

From the same journal

From the same journal

From the same journal

A discrete genetic locus confers xyloglucan metabolism in select human gut Bacteroidetes

Research output: Contribution to journalArticlepeer-review

Published copy (DOI)


  • Johan Larsbrink
  • Theresa E. Rogers
  • Glyn R. Hemsworth
  • Lauren S. McKee
  • Alexandra S. Tauzin
  • Oliver Spadiut
  • Stefan Klinter
  • Nicholas A. Pudlo
  • Karthik Urs
  • Nicole M. Koropatkin
  • A. Louise Creagh
  • Charles A. Haynes
  • Amelia G. Kelly
  • Stefan Nilsson Cederholm
  • Gideon J. Davies
  • Eric C. Martens
  • Harry Brumer


Publication details

DateAccepted/In press - 22 Nov 2013
DateE-pub ahead of print - 19 Jan 2014
DatePublished (current) - 27 Feb 2014
Issue number7489
Number of pages5
Pages (from-to)498-502
Early online date19/01/14
Original languageEnglish


A well-balanced human diet includes a significant intake of non-starch polysaccharides, collectively termed 'dietary fibre', from the cell walls of diverse fruits and vegetables. Owing to the paucity of alimentary enzymes encoded by the human genome, our ability to derive energy from dietary fibre depends on the saccharification and fermentation of complex carbohydrates by the massive microbial community residing in our distal gut. The xyloglucans (XyGs) are a ubiquitous family of highly branched plant cell wall polysaccharides whose mechanism(s) of degradation in the human gut and consequent importance in nutrition have been unclear. Here we demonstrate that a single, complex gene locus in Bacteroides ovatus confers XyG catabolism in this common colonic symbiont. Through targeted gene disruption, biochemical analysis of all predicted glycoside hydrolases and carbohydrate-binding proteins, and three-dimensional structural determination of the vanguard endo-xyloglucanase, we reveal the molecular mechanisms through which XyGs are hydrolysed to component monosaccharides for further metabolism. We also observe that orthologous XyG utilization loci (XyGULs) serve as genetic markers of XyG catabolism in Bacteroidetes, that XyGULs are restricted to a limited number of phylogenetically diverse strains, and that XyGULs are ubiquitous in surveyed human metagenomes. Our findings reveal that the metabolism of even highly abundant components of dietary fibre may be mediated by niche species, which has immediate fundamental and practical implications for gut symbiont population ecology in the context of human diet, nutrition and health. © 2014 Macmillan Publishers Limited.

Bibliographical note

©2014 Macmillan Publishers Limited. All rights reserved


  • Human Microbiota

    Impact: Public Health

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