Chlamydia trachomatis has penicillin-binding proteins but not detectable muramic acid

J Bacteriol. 1982 Jul;151(1):420-8. doi: 10.1128/jb.151.1.420-428.1982.

Abstract

Chlamydia trachomatis LGV-434 was grown in HeLa 229 cells. Benzylpenicillin completely inhibited the formation of infectious elementary bodies (EBs) at a concentration of 19 pmol/ml or higher and produced abnormally large reticulate bodies (RBs) in the inclusions at 30 pmol/ml or higher. The possible targets for penicillin in C. trachomatis were three penicillin-binding proteins (PBPs) which were identified in the Sarkosyl-soluble fractions of both RBs and EBs. The apparent subunit molecular weights were 88,000 (PBP 1), 61,000 (BPB 2), and 36,000 (PBP 3). The 50% binding concentrations of [3H]penicillin for PBPs 1 to 3 in EBs and RBs were between 7 and 70 pmol/ml. Such high susceptibility to penicillin was shown by an organism that did not have detectable muramic acid (less than 0.02% by weight) in preparations of either whole cells or sodium dodecyl sulfate-insoluble residues.

MeSH terms

  • Bacterial Proteins*
  • Biological Assay
  • Biological Transport
  • Carrier Proteins / isolation & purification
  • Carrier Proteins / metabolism*
  • Chlamydia / metabolism*
  • Chlamydia / ultrastructure
  • HeLa Cells / drug effects
  • HeLa Cells / metabolism
  • HeLa Cells / microbiology
  • Hexosyltransferases*
  • Humans
  • Kinetics
  • Microscopy, Electron
  • Muramic Acids / analysis*
  • Muramoylpentapeptide Carboxypeptidase*
  • Penicillin G / metabolism
  • Penicillin G / pharmacology
  • Penicillin-Binding Proteins
  • Penicillins / metabolism*
  • Peptidyl Transferases*
  • Sugar Acids / analysis*

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • Muramic Acids
  • Penicillin-Binding Proteins
  • Penicillins
  • Sugar Acids
  • Peptidyl Transferases
  • Hexosyltransferases
  • Muramoylpentapeptide Carboxypeptidase
  • Penicillin G