Activity studies and crystal structures of catalytically deficient mutants of cellobiohydrolase I from Trichoderma reesei

J Stahlberg, C Divne, A Koivula, K Piens, M Claeyssens, TT Teeri, TA Jones

Research output: Contribution to journalArticleScientificpeer-review

Abstract

The roles of the residues in the catalytic trio Glu212-Asp214-Glu217 in cellobiohydrolase I (CBHI) from Trichoderma reesei have been investigated by changing these residues to their isosteric amide counterparts. Three mutants, E212Q, D214N and E217Q, were constructed and expressed in T. reesei. All three point mutations significantly impair the catalytic activity of the enzyme, although all retain some residual activity. On the small chromophoric substrate CNP-Lac, the k(cat), values were reduced to 1/2000, 1/85 and 1/370 of the wild-type activity, respectively, whereas the K-M values remained essentially unchanged. On insoluble crystalline cellulose, BMCC, no significant activity was detected for the E212Q and E217Q mutants, whereas the D214N mutant retained residual activity. The consequences of the individual mutations on the active-site structure were assessed for two of the mutants, E212Q and D214N, by X-ray crystallography at 2.0 Angstrom and 2.2 Angstrom resolution, respectively. In addition, the structure of E212Q CBHI in complex with the natural product, cellobiose, was determined at 2.0 Angstrom resolution. The active-site structure of each mutant is very similar to that of the wild-type enzyme. In the absence of ligand, the active site of the D214N mutant contains a calcium ion firmly bound to Glu212, whereas that of E212Q does not. This supports our hypothesis that Glu212 is the charged species during catalysis. As in the complex of wild-type CBHI with bound o-iodobenzyl-1-thio-beta-D-glucoside, cellobiose is bound to the two product sites in the complex with E212Q. However, the binding of cellobiose differs from that of the glucoside in that the cellobiose is shifted away from the trio of catalytic residues to interact more intimately with a loop that is part of the outer wall of the active site. (C) 1996 Academic Press Limited

Original languageEnglish
Pages (from-to)337-349
Number of pages13
JournalJOURNAL OF MOLECULAR BIOLOGY
Volume264
Issue number2
Publication statusPublished - 29 Nov 1996
MoE publication typeA1 Journal article-refereed

Keywords

  • cellulase
  • cellobiohydrolase I
  • catalytic activity
  • active-site mutant
  • crystal structure
  • SITE-DIRECTED MUTAGENESIS
  • ACID-SEQUENCE SIMILARITIES
  • FREE R-VALUE
  • GLYCOSYL HYDROLASES
  • ENDOGLUCANASE-I
  • MACROMOLECULAR STRUCTURES
  • 3-DIMENSIONAL STRUCTURE
  • CELLULOLYTIC SYSTEM
  • LIMITED PROTEOLYSIS
  • CELLULOMONAS-FIMI

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