The role of l-arabinose metabolism for Escherichia coli O157:H7 in edible plants
Arabinose is a major plant aldopentose in the form of arabinans complexed in cell wall polysaccharides or glycoproteins (AGP), but comparatively rare as a monosaccharide. l-arabinose is an important bacterial metabolite, accessed by pectolytic micro-organisms such as via pectin and hemicellulose deg...
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Published in | Microbiology (Society for General Microbiology) Vol. 167; no. 7 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Microbiology Society
01.07.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Arabinose is a major plant aldopentose in the form of arabinans complexed in cell wall polysaccharides or glycoproteins (AGP), but comparatively rare as a monosaccharide. l-arabinose is an important bacterial metabolite, accessed by pectolytic micro-organisms such as
via pectin and hemicellulose degrading enzymes. However, not all plant-associated microbes encode cell-wall-degrading enzymes, yet can metabolize l-arabinose, raising questions about their use of and access to the glycan in plants. Therefore, we examined l-arabinose metabolism in the food-borne pathogen
O157:H7 (isolate Sakai) during its colonization of plants. l-arabinose metabolism (
) and transport (
) genes were activated at 18 °C
by l-arabinose and expressed over prolonged periods
. Although deletion of
did not impact the colonization ability of
O157:H7 (Sakai) on spinach and lettuce plants (both associated with STEC outbreaks),
was induced on exposure to spinach cell-wall polysaccharides. Furthermore, debranched and arabinan oligosaccharides induced
metabolism gene expression
, and stimulated modest proliferation, while immobilized pectin did not. Thus,
O157:H7 (Sakai) can utilize pectin/AGP-derived l-arabinose as a metabolite. Furthermore, it differs fundamentally in
gene organization, transport and regulation from the related pectinolytic species
, reflective of distinct plant-associated lifestyles. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work |
ISSN: | 1465-2080 1350-0872 1465-2080 |
DOI: | 10.1099/MIC.0.001070 |