Novel intracellular GH10 xylanase from Cohnella laeviribosi HY-21: biocatalytic properties and alterations of substrate specificities by site-directed mutagenesis of Trp residues

Bioresour Technol. 2010 Nov;101(22):8814-21. doi: 10.1016/j.biortech.2010.06.023. Epub 2010 Jul 7.

Abstract

The novel intracellular GH10 xylanase (iXylC) gene (1023-bp) of Cohnella laeviribosi HY-21 encoded a protein consisting of 340 amino acids with a deduced molecular mass of 39,330Da and a calculated pI of 5.81. The primary structure of iXylC was 70% identical to that of Geobacillus sp. GH10 enzyme (GenBank accession number: EDV78425). Xylanolytic activity of the His-tagged iXylC overproduced in Escherichiacoli BL21 was stimulated by 2.2-fold in the presence of 0.5% non-ionic detergents. iXylC produced a mixture of xylooligosaccharides (xylobiose to xylooctaose) from xylotriose and xylotetraose used as the hydrolytic substrate. In addition, it exhibited considerable cleavage activities for p-nitrophenylxylopyranoside (PNP-xylopyranoside) and PNP-cellobioside, indicating that iXylC is a unique GH10 enzyme. The hydrolytic activity (57.8IUmL(-1)) of iXylC toward PNP-xylopyranoside increased to 8.3-fold by W217A and W315A mutations, while mutations of W133A, W295A, and W303A abolished the hydrolytic activity of the enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Endo-1,4-beta Xylanases / biosynthesis*
  • Endo-1,4-beta Xylanases / genetics*
  • Mutagenesis, Site-Directed / methods*
  • Paenibacillus / physiology*
  • Protein Engineering / methods
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Substrate Specificity
  • Tryptophan / genetics*

Substances

  • Recombinant Proteins
  • Tryptophan
  • Endo-1,4-beta Xylanases