Immunoaffinity purification, stabilization and comparative characterization of listeriolysin O from Listeria monocytogenes serotypes 1/2a and 4b

Res Microbiol. 1992 Jun;143(5):489-98. doi: 10.1016/0923-2508(92)90095-6.

Abstract

We developed a simple and highly effective procedure for stabilizing the haemolytic activity of listeriolysin O (LLO) from Listeria monocytogenes after immunoaffinity purification. The haemolytic activity of LLO was stabilized by eluting it directly into tubes containing an alkaline buffer (5 mM lysine, 140 mM KCl, 50% ethylene glycol, pH 11.5). The purified LLO retained 100% of its haemolytic activity after 6 weeks of storage at -20 degrees C. LLO purified from a strain of L. monocytogenes serotype 1/2a (ATCC 43249) and LLO purified from a strain of L. monocytogenes serotype 4b (F 2365) isolated from a Mexican-style cheese, showed no significant differences in pH and temperature stability. When incubated in buffers at pH values from 4 to 12 at 4 degrees C and 25 degrees C, LLO from serotypes 1/2a and 4b retained maximal haemolytic activity at pH 8 after 4 h of incubation. LLO from both serotypes lost their haemolytic activity after incubation at 50 degrees C for 25 min.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Toxins*
  • Chromatography, Affinity / methods*
  • Drug Stability
  • Heat-Shock Proteins / chemistry
  • Heat-Shock Proteins / isolation & purification*
  • Hemolysin Proteins
  • Hydrogen-Ion Concentration
  • Immunoblotting
  • In Vitro Techniques
  • Listeria monocytogenes / metabolism*
  • Listeria monocytogenes / pathogenicity
  • Virulence

Substances

  • Bacterial Toxins
  • Heat-Shock Proteins
  • Hemolysin Proteins
  • hlyA protein, Listeria monocytogenes