A new cell surface proteinase: sequencing and analysis of the prtB gene from Lactobacillus delbruekii subsp. bulgaricus

J Bacteriol. 1996 Jun;178(11):3059-65. doi: 10.1128/jb.178.11.3059-3065.1996.

Abstract

Investigation of the chromosomal region downstream of the lacZ gene from Lactobacillus delbrueckii subsp. bulgaricus revealed the presence of a gene (prtB) encoding a proteinase of 1,946 residues with a predicted molecular mass of 212 kDa. The deduced amino acid sequence showed that PrtB proteinase displays significant homology with the N termini and catalytic domains of lactococcal PrtP cell surface proteinases and is probably synthesized as a preproprotein. However, the presence of a cysteine near the histidine of the PrtB active site suggests that PrtB belongs to the subfamily of cysteine subtilisins. The C-terminal region strongly differs from those of PrtP proteinases by having a high lysine content, an imperfect duplication of 41 residues, and a degenerated sequence compared with the consensus sequence for proteins anchoring in the cell walls of gram-positive bacteria. Finally, the product of the truncated prtM-like gene located immediately upstream of the prtB gene seems too short to be involved in the maturation of PrtB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics*
  • Base Sequence
  • Binding Sites
  • DNA, Bacterial / chemistry
  • Endopeptidases / chemistry
  • Endopeptidases / genetics*
  • Genes, Bacterial*
  • Lactobacillus / enzymology
  • Lactobacillus / genetics*
  • Membrane Proteins / genetics*
  • Molecular Sequence Data
  • Serine Endopeptidases*

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • Membrane Proteins
  • Endopeptidases
  • Serine Endopeptidases
  • lactocepin
  • PrtB protein, bacteria

Associated data

  • GENBANK/L48487