Characterization and properties of an LL-oligopeptidase from sporulating cells of Bacillus sphaericus

J Bacteriol. 1981 Feb;145(2):675-80. doi: 10.1128/jb.145.2.675-680.1981.

Abstract

An LL-oligopeptidase was characterized in the cell cytoplasm of sporulating Bacillus sphaericus 9602. Its activity showed a threefold increase throughout sporulation. The enzyme has lytic activity on various LL-dipeptides, especially on dipeptides with N-terminal L-alanine. Lytic activity was also found on some tripeptides and larger peptides which contain the sequence L-Ala-L-Ala. The role of this oligopeptidase in relation to sporulation may be to supply the cell with L-alanine for the biosynthesis of the peptide chains of the spore cortex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus / enzymology*
  • Bacillus / physiology
  • Exopeptidases
  • Oligopeptides
  • Peptide Hydrolases / metabolism*
  • Peptidyl Transferases / metabolism
  • Spores, Bacterial / enzymology
  • Substrate Specificity

Substances

  • Oligopeptides
  • Peptidyl Transferases
  • Exopeptidases
  • Peptide Hydrolases
  • oligopeptidase