Skip to main content

Research Repository

Advanced Search

Structure–function characterization reveals new catalytic diversity in the galactose oxidase and glyoxal oxidase family

Yin, DeLu; Urresti, Saioa; Lafond, Mickael; Johnston, Esther M.; Derikvand, Fatemeh; Ciano, Luisa; Berrin, Jean-Guy; Henrissat, Bernard; Walton, Paul H.; Davies, Gideon J.; Brumer, Harry

Structure–function characterization reveals new catalytic diversity in the galactose oxidase and glyoxal oxidase family Thumbnail


Authors

DeLu Yin

Saioa Urresti

Mickael Lafond

Esther M. Johnston

Fatemeh Derikvand

Jean-Guy Berrin

Bernard Henrissat

Paul H. Walton

Gideon J. Davies

Harry Brumer



Abstract

Alcohol oxidases, including carbohydrate oxidases, have a long history of research that has generated fundamental biological understanding and biotechnological applications. Despite a long history of study, the galactose 6-oxidase/glyoxal oxidase family of mononuclear copper-radical oxidases, Auxiliary Activity Family 5 (AA5), is currently represented by only very few characterized members. Here we report the recombinant production and detailed structure–function analyses of two homologues from the phytopathogenic fungi Colletotrichum graminicola and C. gloeosporioides, CgrAlcOx and CglAlcOx, respectively, to explore the wider biocatalytic potential in AA5. EPR spectroscopy and crystallographic analysis confirm a common active-site structure vis-à-vis the archetypal galactose 6-oxidase from Fusarium graminearum. Strikingly, however, CgrAlcOx and CglAlcOx are essentially incapable of oxidizing galactose and galactosides, but instead efficiently catalyse the oxidation of diverse aliphatic alcohols. The results highlight the significant potential of prospecting the evolutionary diversity of AA5 to reveal novel enzyme specificities, thereby informing both biology and applications.

Journal Article Type Article
Acceptance Date Nov 16, 2015
Online Publication Date Dec 18, 2015
Publication Date 2015-12
Deposit Date Feb 13, 2020
Publicly Available Date Feb 21, 2020
Journal Nature Communications
Electronic ISSN 2041-1723
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 6
Issue 1
Article Number 10197
DOI https://doi.org/10.1038/ncomms10197
Public URL https://nottingham-repository.worktribe.com/output/3829518
Publisher URL https://www.nature.com/articles/ncomms10197
Additional Information Received: 23 June 2015; Accepted: 16 November 2015; First Online: 18 December 2015; : The authors declare no competing financial interests.

Files






You might also like



Downloadable Citations