Literature DB >> 164911

Interaction of Clostridium perfringens theta-haemolysin, a contaminant of commercial phospholipase C, with erythrocyte ghost membranes and lipid dispersions. A morphological study.

C J Smyth, J H Freer, J P Arbuthnott.   

Abstract

Commercially available preparations of phospholipase C from Clostridium perfringens are commonly contaminated with theta haemolysin, one of a group of bacterial haemolysins called oxygen labile (O-labile) haemolysins. Treatment of erythrocyte ghosts and a mixed lipid dispersion containing cholesterol with commercially available phospholipase C in the absence of Ca-2+ and the presence of phosphate buffer and/or EDTA resulted in the formation and release of ring or arc-shaped structures. Highly purified phospholipase C, free of theta-haemolysin, produced no changes in the morphology of erythrocyte ghosts or lipid dispersions in the presence of phosphate or EDTA, but caused the formation of typical diglyceride droplets in the presence of Ca-2+ in the absence of these inhibitors. Ring structures, identical to those caused by commercial phospholipase C, were formed on addition of highly purified theta-haemolysin to erythrocyte ghost membranes, lipid dispersions containing cholesterol and cholesterol dispersions, but not on treatment of membranes from Micrococcus lysodeikticus. Heat-inactivated O-haemolysin (60 degrees C for 10 min) produced no such effects. The dimensions of rings and arcs displayed heterogeneity. The outside diameters in various preparations varied from approx. 27-58 nm with border thickness of 4.1-7.8 nm.

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Year:  1975        PMID: 164911     DOI: 10.1016/0005-2736(75)90216-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  7 in total

1.  Use of a monoclonal antibody to determine the mode of transmembrane pore formation by streptolysin O.

Authors:  F Hugo; J Reichwein; M Arvand; S Krämer; S Bhakdi
Journal:  Infect Immun       Date:  1986-12       Impact factor: 3.441

2.  Mechanism of membrane damage by streptolysin-O.

Authors:  S Bhakdi; J Tranum-Jensen; A Sziegoleit
Journal:  Infect Immun       Date:  1985-01       Impact factor: 3.441

3.  Interaction of streptolysin O from Streptococcus pyogenes and theta-toxin from Clostridium perfringens with human fibroblasts.

Authors:  M Thelestam; R Möllby
Journal:  Infect Immun       Date:  1980-09       Impact factor: 3.441

4.  Phosphatidic acid and phosphatidylinositol labelling in adipose tissue. Relationship to the metabolic effects of insulin and insulin-like agents.

Authors:  T W Honeyman; W Strohsnitter; C R Scheid; R J Schimmel
Journal:  Biochem J       Date:  1983-05-15       Impact factor: 3.857

5.  Molecular cloning and nucleotide sequence of the alpha-toxin (phospholipase C) of Clostridium perfringens.

Authors:  R W Titball; S E Hunter; K L Martin; B C Morris; A D Shuttleworth; T Rubidge; D W Anderson; D C Kelly
Journal:  Infect Immun       Date:  1989-02       Impact factor: 3.441

6.  Evidence for coupling of Clostridium perfringens alpha-toxin-induced hemolysis to stimulated phosphatidic acid formation in rabbit erythrocytes.

Authors:  J Sakurai; S Ochi; H Tanaka
Journal:  Infect Immun       Date:  1993-09       Impact factor: 3.441

7.  Effect of streptolysin O on erythrocyte membranes, liposomes, and lipid dispersions. A protein-cholesterol interaction.

Authors:  J L Duncan; R Schlegel
Journal:  J Cell Biol       Date:  1975-10       Impact factor: 10.539

  7 in total

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