Impact of peptidoglycan O-acetylation on autolytic activities of the Enterococcus faecalis N-acetylglucosaminidase AtlA and N-acetylmuramidase AtlB

FEBS Lett. 2009 Sep 17;583(18):3033-8. doi: 10.1016/j.febslet.2009.08.010. Epub 2009 Aug 15.

Abstract

Autolysins are potentially lethal enzymes that partially hydrolyze peptidoglycan for incorporation of new precursors and septum cleavage after cell division. Here, we explored the impact of peptidoglycan O-acetylation on the enzymatic activities of Enterococcus faecalis major autolysins, the N-acetylglucosaminidase AtlA and the N-acetylmuramidase AtlB. We constructed isogenic strains with various O-acetylation levels and used them as substrates to assay E. faecalis autolysin activities. Peptidoglycan O-acetylation had a marginal inhibitory impact on the activities of these enzymes. In contrast, removal of cell wall glycopolymers increased the AtlB activity (37-fold), suggesting that these polymers negatively control the activity of this enzyme.

MeSH terms

  • Acetylation
  • Acetylglucosaminidase / metabolism*
  • Bacteriolysis*
  • Cell Wall / chemistry
  • Enterococcus faecalis / enzymology*
  • Enterococcus faecalis / physiology
  • Glycoside Hydrolases / metabolism*
  • Peptidoglycan / metabolism*

Substances

  • Peptidoglycan
  • Glycoside Hydrolases
  • endo-N-acetylmuramidase
  • Acetylglucosaminidase