Specificity for various imino-acid-residues of a proline-specific dipeptidylcarboxypeptidase from a Streptomyces species

Biochim Biophys Acta. 1993 Mar 5;1162(1-2):72-6. doi: 10.1016/0167-4838(93)90129-f.

Abstract

A proline-specific dipeptidylcarboxypeptidase, which removes diproline from the C-terminus of the proline-containing peptides, such as Boc-Pro-Pro-Pro-Pro and Leu-Pro-Pro-Pro-Pro-Pro, has recently been purified from a Streptomyces sp. The specificity of the enzyme for various imino acid-containing synthetic peptide substrates was further studied. The peptides with proline, hydroxyproline, or dehydroproline at the P2' position were found to be good substrates, while those with pipecolic acid, D-proline or other usual amino acids at the P2' position were scarcely hydrolyzed. The peptides with proline, dehydroproline, pipecolic acid, or N-methyl-alanine at the P1' position were well-hydrolyzed, while those with hydroxyproline or D-proline at the P1' position were not hydrolyzed. Utilizing this high specificity for imino acids, Boc-Pro-Pro-Pro-Pro was synthesized by the enzyme using Boc-Pro-Pro as the acidic component and Pro-Pro as the basic component.

MeSH terms

  • Amino Acid Sequence
  • Carboxypeptidases / isolation & purification
  • Carboxypeptidases / metabolism*
  • Endopeptidases / isolation & purification
  • Endopeptidases / metabolism*
  • Hydrolysis
  • Imino Acids / metabolism*
  • Molecular Sequence Data
  • Peptide Biosynthesis
  • Peptides / metabolism
  • Proline / metabolism*
  • Stereoisomerism
  • Streptomyces / enzymology*
  • Substrate Specificity

Substances

  • Imino Acids
  • Peptides
  • Proline
  • Carboxypeptidases
  • Endopeptidases
  • proline-specific dipeptidylcarboxypeptidase