Site-directed mutagenesis of the Streptomyces R61 DD-peptidase. Catalytic function of the conserved residues around the active site and a comparison with class-A and class-C beta-lactamases

Eur J Biochem. 1992 Jul 1;207(1):97-102. doi: 10.1111/j.1432-1033.1992.tb17025.x.

Abstract

The importance of various residues in the Streptomyces R61 penicillin-sensitive DD-peptidase has been assessed by site-directed mutagenesis. The replacement of the active Ser62 by a Cys residue yielded an inactive protein which was also unable to recognize penicillin. The activity of the Lys65----Arg mutant with the peptide and thiolester substrates was decreased 100-200-fold and the rate of penicillin inactivation was decreased 20,000-fold or more. The mutant thus behaved as a poor, but penicillin-resistant, DD-peptidase. The other studied mutations, the mutations Phe58----Leu, Tyr90----Asn, Thr101----Asn, Phe164----Ala, Asp225----Glu and Asp225----Asn had little influence on the catalytic and penicillin-binding properties. The Asp225 mutants did not exhibit an increased sensitivity to cefotaxime. The Phe164----Ala mutant was significantly more unstable than the wild-type enzyme.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Binding Sites
  • Kinetics
  • Molecular Sequence Data
  • Muramoylpentapeptide Carboxypeptidase / genetics
  • Muramoylpentapeptide Carboxypeptidase / metabolism*
  • Mutagenesis, Site-Directed*
  • Oligodeoxyribonucleotides
  • Streptomyces / enzymology*
  • Streptomyces / genetics
  • Substrate Specificity
  • beta-Lactamases / genetics
  • beta-Lactamases / metabolism*

Substances

  • Oligodeoxyribonucleotides
  • Muramoylpentapeptide Carboxypeptidase
  • beta-Lactamases