Detection of a gonococcal endo-beta-N-acetyl-D-glucosaminidase and its peptidoglycan cleavage site

J Bacteriol. 1982 Jul;151(1):172-6. doi: 10.1128/jb.151.1.172-176.1982.

Abstract

Neisseria gonorrhoeae contains several hydrolases which may be responsible for gonococcal cell lysis. One of these enzymes, an endo-beta-N-acetyl-D-glucosaminidase, has been extracted from supernatants of sonicated gonococci and partially purified by ammonium sulfate precipitation and affinity and ion-exchange chromatography. This enzyme has a different specificity than egg white lysozyme and cleaves the beta 1 leads to 4 glycosidic linkage between N-acetylglucosamine and N-acetylmuramic acid in gonococcal peptidoglycan.

MeSH terms

  • Acetylglucosaminidase / isolation & purification
  • Acetylglucosaminidase / metabolism*
  • Hexosaminidases / metabolism*
  • Kinetics
  • Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase
  • Neisseria gonorrhoeae / enzymology*
  • Peptidoglycan
  • Substrate Specificity

Substances

  • Peptidoglycan
  • Hexosaminidases
  • Acetylglucosaminidase
  • Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase