Affiliation:
1. Department of Biochemistry University of Cambridge Hopkins Building, The Downing Site, Tennis Court Road Cambridge CB2 1QW UK
2. Department of Plant Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology Jagiellonian University Gronostajowa 7 Krakow 30‐387 Poland
3. Novozymes A/S Krogshøjvej 36 2880 Bagsværd Denmark
Abstract
Summary
Polysaccharide structural complexity not only influences cell wall strength and extensibility but also hinders pathogenic and biotechnological attempts to saccharify the wall. In certain species and tissues, glucuronic acid side groups on xylan exhibit arabinopyranose or galactose decorations whose genetic and evolutionary basis is completely unknown, impeding efforts to understand their function and engineer wall digestibility.
Genetics and polysaccharide profiling were used to identify the responsible loci in Arabidopsis and Eucalyptus from proposed candidates, while phylogenies uncovered a shared evolutionary origin. GH30‐family endo‐glucuronoxylanase activities were analysed by electrophoresis, and their differing specificities were rationalised by phylogeny and structural analysis.
The newly identified xylan arabinopyranosyltransferases comprise an overlooked subfamily in the GT47‐A family of Golgi glycosyltransferases, previously assumed to comprise mainly xyloglucan galactosyltransferases, highlighting an unanticipated adaptation of both donor and acceptor specificities. Further neofunctionalisation has produced a Myrtaceae‐specific xylan galactosyltransferase. Simultaneously, GH30 endo‐glucuronoxylanases have convergently adapted to overcome these decorations, suggesting a role for these structures in defence. The differential expression of glucuronoxylan‐modifying genes across Eucalyptus tissues, however, hints at further functions.
Our results demonstrate the rapid adaptability of biosynthetic and degradative carbohydrate‐active enzyme activities, providing insight into plant–pathogen interactions and facilitating plant cell wall biotechnological utilisation.
Funder
Novo Nordisk Foundation Center for Basic Metabolic Research
UK Research and Innovation
Biotechnology and Biological Sciences Research Council
Cited by
2 articles.
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