Temperature-dependent inactivating factor of Pseudomonas aeruginosa exotoxin A

Infect Immun. 1976 May;13(5):1467-72. doi: 10.1128/iai.13.5.1467-1472.1976.

Abstract

The adenosine diphosphate ribosyl transferase activity of Pseudomonas aeruginosa exotoxin A(PA toxin) was found to be rapidly destroyed by heating at 45 to 60C but not by heating at 70 to 90C (for at least 30 min). This phenomenon has been previously described for other bacterial toxins (staphylococcal alpha-toxin and Vibrio parahaemolyticus hemolysin) and is termed an Arrhenius effect. In contrast, the Arrhenius effect was not seen when the PA toxin was heat-treated as above and tested for cell toxicity or mouse lethality. Although the PA toxin treated at 70C for 30 min retained a significant proportion (is greater than 70%) of its adenosine diphosphate ribosyl transferase activity, the cell toxicity and mouse lethality of the toxin were virtually abolished. A temperature-dependent inactivating factor that has proteolytic activity and is co-purified with the PA toxin was shown to be responsible for the Arrhenius effect. PA toxin separated from the factor by conventional disc gel electrophoresis or PA toxin preparations lacking the factor did not show the Arrhenius effect.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • ADP Ribose Transferases
  • Animals
  • Bacterial Toxins
  • Cell Survival
  • Electrophoresis, Polyacrylamide Gel
  • Exotoxins
  • Hot Temperature
  • In Vitro Techniques
  • L Cells / metabolism
  • Lethal Dose 50
  • Mice
  • NAD+ Nucleosidase / analysis
  • Peptide Hydrolases / analysis
  • Pseudomonas aeruginosa / metabolism*
  • Pseudomonas aeruginosa Exotoxin A
  • Temperature*
  • Toxins, Biological / isolation & purification
  • Toxins, Biological / pharmacology*
  • Virulence Factors

Substances

  • Bacterial Toxins
  • Exotoxins
  • Toxins, Biological
  • Virulence Factors
  • ADP Ribose Transferases
  • NAD+ Nucleosidase
  • Peptide Hydrolases