Endoglucanase 28 (Cel12A), a new Phanerochaete chrysosporium cellulase

Eur J Biochem. 1999 Jan;259(1-2):88-95. doi: 10.1046/j.1432-1327.1999.00011.x.

Abstract

A 28-kDa endoglucanase was isolated from the culture filtrate of Phanerochaete chrysosporium strain K3 and named EG 28. It degrades carboxymethylated cellulose and amorphous cellulose, and to a lesser degree xylan and mannan but not microcrystalline cellulose (Avicel). EG 28 is unusual among cellulases from aerobic fungi, in that it appears to lack a cellulose-binding domain and does not bind to crystalline cellulose. The enzyme is efficient at releasing short fibres from filter paper and mechanical pulp, and acts synergistically with cellobiohydrolases. Its mode of degrading filter paper appears to be different to that of endoglucanase I from Trichoderma reesei. Furthermore, EG 28 releases colour from stained cellulose beads faster than any other enzyme tested. Peptide mapping suggests that it is not a fragment of another known endoglucanases from P. chrysosporium and peptide sequences indicate that it belongs to family 12 of the glycosyl hydrolases. EG 28 is glycosylated. The biological function of the enzyme is discussed, and it is hypothesized that it is homologous to EG III in Trichoderma reesei and the role of the enzyme is to make the cellulose in wood more accessible to other cellulases.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cellulase / isolation & purification
  • Cellulase / metabolism*
  • Cellulose / metabolism
  • Glucosides / metabolism
  • Mannans / metabolism
  • Molecular Sequence Data
  • Peptide Mapping
  • Phanerochaete / enzymology*
  • Sequence Homology, Amino Acid
  • Substrate Specificity
  • Xylans / metabolism

Substances

  • Glucosides
  • Mannans
  • Xylans
  • 4-nitrophenyl beta-cellobioside
  • Cellulose
  • Cellulase