Isolation and characterization of a subtilisin-like proteinase of Bacillus intermedius secreted by the Bacillus subtilis recombinant strain AJ73 at different growth stages

Biochemistry (Mosc). 2007 Feb;72(2):192-8. doi: 10.1134/s0006297907020095.

Abstract

Two subtilisin-like serine proteinases of Bacillus intermedius secreted by the Bacillus subtilis recombinant strain AJ73 (pCS9) on the 28th and 48th h of culture growth (early and late proteinase, respectively) have been isolated by ion-exchange chromatography on CM-cellulose and by FPLC. Molecular weights of both proteinases were determined. The N-terminal sequences of the recombinant protein and mature proteinases of the original strain were compared. Kinetic parameters and substrate specificities of the early and late proteinase were analyzed. Physicochemical properties of the enzymes were studied.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacillus / enzymology*
  • Bacillus / genetics
  • Bacillus / growth & development
  • Bacillus subtilis / enzymology*
  • Bacillus subtilis / genetics
  • Bacillus subtilis / growth & development
  • Chromatography, Ion Exchange
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Recombinant Proteins* / chemistry
  • Recombinant Proteins* / genetics
  • Recombinant Proteins* / isolation & purification
  • Recombinant Proteins* / metabolism
  • Serine Endopeptidases* / chemistry
  • Serine Endopeptidases* / genetics
  • Serine Endopeptidases* / isolation & purification
  • Serine Endopeptidases* / metabolism
  • Substrate Specificity
  • Subtilisin* / chemistry
  • Subtilisin* / genetics
  • Subtilisin* / isolation & purification
  • Subtilisin* / metabolism
  • Temperature

Substances

  • Recombinant Proteins
  • Serine Endopeptidases
  • Subtilisin