Characterization of a new sigma-K-dependent peptidoglycan hydrolase gene that plays a role in Bacillus subtilis mother cell lysis

J Bacteriol. 1999 Oct;181(20):6230-7. doi: 10.1128/JB.181.20.6230-6237.1999.

Abstract

Bacillus subtilis produces a 30-kDa peptidoglycan hydrolase, CwlH, during the late sporulation phase. Disruption of yqeE led to a complete loss of CwlH formation, indicating the identity of yqeE with cwlH. Northern blot analysis of cwlH revealed a 0.8-kb transcript after 6 to 7.5 h for the wild-type strain but not for the sigma(F), sigma(E), sigma(G), and sigma(K) mutants. Expression of the sigma(K)-dependent cwlH gene depended on gerE. Primer extension analysis also suggested that cwlH is transcribed by Esigma(K) RNA polymerase. CwlH produced in Escherichia coli harboring a cwlH plasmid is an N-acetylmuramoyl-L-alanine amidase (EC 3.5.1.28) and exhibited an optimum pH of 7.0 and high-level binding to the B. subtilis cell wall. A cwlC cwlH double mutation led to a lack of mother cell lysis even after 7 days of incubation in DSM medium, but the single mutations led to mother cell lysis after 24 h.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacillus subtilis / cytology
  • Bacillus subtilis / physiology*
  • Bacterial Proteins*
  • Bacteriolysis / physiology*
  • Base Sequence
  • Cell Wall / metabolism
  • Gene Expression Regulation, Bacterial
  • Gene Expression Regulation, Enzymologic
  • Genes, Bacterial*
  • Molecular Sequence Data
  • N-Acetylmuramoyl-L-alanine Amidase / genetics
  • N-Acetylmuramoyl-L-alanine Amidase / metabolism*
  • Protein Binding
  • Sequence Homology, Amino Acid
  • Spores, Bacterial / physiology
  • Substrate Specificity
  • Transcription Factors / metabolism*

Substances

  • Bacterial Proteins
  • Transcription Factors
  • sigma K
  • CwlH protein, Bacillus subtilis
  • N-Acetylmuramoyl-L-alanine Amidase