Cell wall branches, penicillin resistance and the secrets of the MurM protein

Trends Microbiol. 2003 Dec;11(12):547-53. doi: 10.1016/j.tim.2003.10.003.

Abstract

Production of low-affinity forms of penicillin-binding proteins (PBPs), although essential, is not sufficient to protect pneumococci against the inhibitory action of penicillin. Resistance also requires the newly identified protein MurM which, together with MurN, is involved with the synthesis of short peptide branches in the pneumococcal cell wall. Cells in which murM was inactivated produced cell walls without branches and also completely lost penicillin resistance. To understand these surprising observations a 3D-model of MurM was constructed, which helped to put into structural context several of the biochemical and genetic observations made about this protein.

MeSH terms

  • Bacteria / drug effects
  • Bacteria / metabolism*
  • Bacteria / ultrastructure
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / physiology
  • Carrier Proteins / physiology
  • Cell Wall / chemistry
  • Cell Wall / metabolism
  • Cell Wall / ultrastructure
  • Hexosyltransferases / physiology
  • Models, Molecular
  • Muramoylpentapeptide Carboxypeptidase / physiology
  • Penicillin Resistance*
  • Penicillin-Binding Proteins
  • Peptide Synthases / chemistry*
  • Peptide Synthases / physiology*
  • Peptidoglycan / biosynthesis*
  • Peptidyl Transferases / physiology
  • Streptococcus pneumoniae / drug effects
  • Streptococcus pneumoniae / metabolism
  • Streptococcus pneumoniae / ultrastructure

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • Penicillin-Binding Proteins
  • Peptidoglycan
  • Peptidyl Transferases
  • Hexosyltransferases
  • Muramoylpentapeptide Carboxypeptidase
  • MurM protein, Streptococcus pneumoniae
  • MurN protein, Streptococcus pneumoniae
  • Peptide Synthases