Characterization of the four GH12 Endoxylanases from the plant pathogen Fusarium graminearum

J Microbiol Biotechnol. 2012 Aug;22(8):1118-26. doi: 10.4014/jmb.1112.11019.

Abstract

Four putative GH12 genes were found in the Fusarium graminearum genome. The corresponding proteins were expressed in Escherichia coli, purified, and evaluated. FGSG_05851 and FGSG_11037 displayed high activities towards xyloglucan (V(max) of 4 and 11 micronmol/min, respectively), whereas FGSG_07892 and FGSG_16349 were much less active with this substrate (0.081 and 0.004 micronmol/min, respectively). However, all four of these enzymes had a similar binding affinity for xyloglucan. Xyloglucan was the substrate preferred by FGSG_05851, in contrast to the three other enzymes, which preferred beta-glucan or lichenan. Therefore, FGSG_05851 is a xyloglucan-specific glucanase (E.C. 3.2.1.151) rather than an endoglucanase (E.C. 3.2.1.4) with broad substrate specificity. FGSG_11037 displayed a peculiar behavior in that the xyloglucan binding was highly cooperative, with a Hill coefficient of 2.5. Finally, FGSG_05851 essentially degraded xyloglucan into hepta-, octa-, and nonasaccharides, whereas the three other enzymes yielded hepta- and octa-saccharides as well as larger molecules.

MeSH terms

  • Cloning, Molecular
  • Endo-1,4-beta Xylanases / genetics
  • Endo-1,4-beta Xylanases / isolation & purification
  • Endo-1,4-beta Xylanases / metabolism*
  • Escherichia coli / genetics
  • Fusarium / enzymology*
  • Fusarium / genetics
  • Fusarium / isolation & purification
  • Gene Expression
  • Glucans / metabolism
  • Plant Diseases / microbiology
  • Plants / microbiology
  • Protein Binding
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Substrate Specificity
  • Xylans / metabolism

Substances

  • Glucans
  • Recombinant Proteins
  • Xylans
  • xyloglucan
  • Endo-1,4-beta Xylanases
  • lichenin