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Carbohydrate-active enzymes from Akkermansia muciniphila break down mucin O-glycans to completion

  • Cassie R. Bakshani
  • , Taiwo O. Ojuri
  • , Bo Pilgaard
  • , Jesper Holck
  • , Ross McInnes
  • , Radoslaw P. Kozak
  • , Maria Zakhour
  • , Sara Çakaj
  • , Manon Kerouedan
  • , Emily Newton
  • , David N. Bolam
  • , Lucy I. Crouch*
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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Abstract

Akkermansia muciniphila is a human microbial symbiont residing in the mucosal layer of the large intestine. Its main carbon source is the highly heterogeneous mucin glycoprotein, and it uses an array of carbohydrate-active enzymes and sulfatases to access this complex energy source. Here we describe the biochemical characterization of 54 glycoside hydrolases, 11 sulfatases and 1 polysaccharide lyase from A. muciniphila to provide a holistic understanding of their carbohydrate-degrading activities. This was achieved using a variety of liquid chromatography techniques, mass spectrometry, enzyme kinetics and thin-layer chromatography. These results are supported with A. muciniphila growth and whole-cell assays. We find that these enzymes can act synergistically to degrade the O-glycans on the mucin polypeptide to completion, down to the core N-acetylgalactosaime. In addition, these enzymes can break down human breast milk oligosaccharide, ganglioside and globoside glycan structures, showing their capacity to target a variety of host glycans. These data provide a resource to understand the full degradative capability of the gut microbiome member A. muciniphila.
Original languageEnglish
Pages (from-to)585-598
Number of pages14
JournalNature Microbiology
Volume10
Issue number2
Early online date31 Jan 2025
DOIs
Publication statusPublished - 1 Feb 2025

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