Structural insights into the inhibition of cellobiohydrolase Cel7A by xylo-oligosaccharides

Abstract

The filamentous fungus Hypocreajecorina (anamorph of Trichodermareesei) is the predominant source of enzymes for industrial saccharification of lignocellulose biomass. The major enzyme, cellobiohydrolase Cel7A, constitutes nearly half of the total protein in the secretome. The performance of such enzymes is susceptible to inhibition by compounds liberated by physico-chemical pre-treatment if the biomass is kept unwashed. Xylan and xylo-oligosaccharides (XOS) have been proposed to play a key role in inhibition of cellobiohydrolases of glycoside hydrolase family7. To elucidate the mechanism behind this inhibition at a molecular level, we used X-ray crystallography to determine structures of H.jecorina Cel7A in complex with XOS. Structures with xylotriose, xylotetraose and xylopentaose revealed a predominant binding mode at the entrance of the substrate-binding tunnel of the enzyme, in which each xylose residue is shifted similar to 2.4 angstrom towards the catalytic center compared with binding of cello-oligosaccharides. Furthermore, partial occupancy of two consecutive xylose residues at subsites -2 and -1 suggests an alternative binding mode for XOS in the vicinity of the catalytic center. Interestingly, the -1 xylosyl unit exhibits an open aldehyde conformation in one of the structures and a ring-closed pyranoside in another complex. Complementary inhibition studies with p-nitrophenyl lactoside as substrate indicate mixed inhibition rather than pure competitive inhibition.DatabaseThe atomic coordinates and structure factors are available in the Protein Data Bank under accession number (H. jecorina Cel7A E212Q variant, complex with xylotriose), (H. jecorina Cel7A E217Q variant, complex with xylotriose), (H. jecorina Cel7A E212Q variant, complex with xylopentaose), (H. jecorina Cel7A E217Q variant, complex with xylopentaose), (wild-type H. jecorina Cel7A, complex with xylopentaose) and (H. jecorina Cel7A E217Q variant, complex with xylotetraose).

Keywords

biomass degradation; cellobiose; cellulase; inhibition; xylooligosaccharide

Published in

FEBS Journal
2015, Volume: 282, number: 11, pages: 2167-2177
Publisher: WILEY-BLACKWELL

SLU Authors

• Haddad Momeni, Majid

  • The Department of Chemistry and Biotechnology, Swedish University of Agricultural Sciences
    

• Sandgren, Mats

  • The Department of Chemistry and Biotechnology, Swedish University of Agricultural Sciences
    

• Ståhlberg, Jerry

  • The Department of Chemistry and Biotechnology, Swedish University of Agricultural Sciences
    

• Hansson, Henrik

  • The Department of Chemistry and Biotechnology, Swedish University of Agricultural Sciences
    

UKÄ Subject classification

Biochemistry and Molecular Biology
Structural Biology


Publication identifier

DOI: https://doi.org/10.1111/febs.13265

Permanent link to this page (URI)

https://res.slu.se/id/publ/68449