Proton-binding capacity of Staphylococcus aureus wall teichoic acid and its role in controlling autolysin activity

PLoS One. 2012;7(7):e41415. doi: 10.1371/journal.pone.0041415. Epub 2012 Jul 23.

Abstract

Wall teichoic acid (WTA) or related polyanionic cell wall glycopolymers are produced by most gram-positive bacterial species and have been implicated in various cellular functions. WTA and the proton gradient across bacterial membranes are known to control the activity of autolysins but the molecular details of these interactions are poorly understood. We demonstrate that WTA contributes substantially to the proton-binding capacity of Staphylococcus aureus cell walls and controls autolysis largely via the major autolysin AtlA whose activity is known to decline at acidic pH values. Compounds that increase or decrease the activity of the respiratory chain, a main source of protons in the cell wall, modulated autolysis rates in WTA-producing cells but did not affect the augmented autolytic activity observed in a WTA-deficient mutant. We propose that WTA represents a cation-exchanger like mesh in the gram-positive cell envelopes that is required for creating a locally acidified milieu to govern the pH-dependent activity of autolysins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azides / pharmacology
  • Bacterial Proteins / metabolism
  • Bacteriolysis / drug effects
  • Binding Sites
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cell Wall / drug effects
  • Cell Wall / metabolism*
  • Electron Transport / drug effects
  • Glucose / pharmacology
  • Membrane Potentials / drug effects
  • Models, Biological
  • N-Acetylmuramoyl-L-alanine Amidase / metabolism*
  • Phosphates / metabolism
  • Protons*
  • Staphylococcus aureus / cytology*
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / metabolism*
  • Teichoic Acids / metabolism*

Substances

  • Azides
  • Bacterial Proteins
  • Phosphates
  • Protons
  • Teichoic Acids
  • N-Acetylmuramoyl-L-alanine Amidase
  • Glucose