Broad-specificity GH131 β-glucanases are a hallmark of fungi and oomycetes that colonize plants.
Journal
Environmental microbiology
ISSN: 1462-2920
Titre abrégé: Environ Microbiol
Pays: England
ID NLM: 100883692
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
30
05
2018
revised:
17
02
2019
accepted:
17
03
2019
pubmed:
20
3
2019
medline:
15
4
2020
entrez:
20
3
2019
Statut:
ppublish
Résumé
Plant-tissue-colonizing fungi fine-tune the deconstruction of plant-cell walls (PCW) using different sets of enzymes according to their lifestyle. However, some of these enzymes are conserved among fungi with dissimilar lifestyles. We identified genes from Glycoside Hydrolase family GH131 as commonly expressed during plant-tissue colonization by saprobic, pathogenic and symbiotic fungi. By searching all the publicly available genomes, we found that GH131-coding genes were widely distributed in the Dikarya subkingdom, except in Taphrinomycotina and Saccharomycotina, and in phytopathogenic Oomycetes, but neither other eukaryotes nor prokaryotes. The presence of GH131 in a species was correlated with its association with plants as symbiont, pathogen or saprobe. We propose that GH131-family expansions and horizontal-gene transfers contributed to this adaptation. We analysed the biochemical activities of GH131 enzymes whose genes were upregulated during plant-tissue colonization in a saprobe (Pycnoporus sanguineus), a plant symbiont (Laccaria bicolor) and three hemibiotrophic-plant pathogens (Colletotrichum higginsianum, C. graminicola, Zymoseptoria tritici). These enzymes were all active on substrates with β-1,4, β-1,3 and mixed β-1,4/1,3 glucosidic linkages. Combined with a cellobiohydrolase, GH131 enzymes enhanced cellulose degradation. We propose that secreted GH131 enzymes unlock the PCW barrier and allow further deconstruction by other enzymes during plant tissue colonization by symbionts, pathogens and saprobes.
Identifiants
pubmed: 30887618
doi: 10.1111/1462-2920.14596
doi:
Substances chimiques
Glycoside Hydrolases
EC 3.2.1.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
2724-2739Subventions
Organisme : French National Agency for Research
ID : ANR-11-IDEX-0001-02
Pays : International
Organisme : French National Agency for Research
ID : ANR-13-BIME-0002
Pays : International
Organisme : French National Agency for Research
ID : ANR-14-CE06-0020-01
Pays : International
Organisme : Office of Science of the U.S. Department of Energy
ID : DE-AC02-05CH11231
Pays : International
Organisme : Seventh Framework Programme
ID : FP7-26719
Pays : International
Organisme : EU's Seventh Framework Programme
ID : FP7-26719
Pays : International
Informations de copyright
© 2019 Society for Applied Microbiology and John Wiley & Sons Ltd.