Literature DB >> 170205

Affinity chromatography purification of Clostridium perfringens enterotoxin.

V N Scott, C L Duncan.   

Abstract

Anti-enterotoxin immunoglobulins immobilized on CH-Sepharose or CNBr-Sepharose were used for affinity chromatography purification of Clostridium perfringens enterotoxin. Cell extracts containing enterotoxin or partially purified toxin preparations were applied to the column and nonspecifically-bound protein was eluted. NaOH was used to elute specifically bound toxin. The purity of enterotoxin purified by Sephadex G-100 chromatography followed by affinity chromatography appears similar to toxin highly purified by conventional means. The procedure can be used successfully for the rapid (less than 2 h) purification of small amounts of enterotoxin.

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Year:  1975        PMID: 170205      PMCID: PMC415320          DOI: 10.1128/iai.12.3.536-543.1975

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  25 in total

1.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

2.  Time of enterotoxin formation and release during sporulation of Clostridium perfringens type A.

Authors:  C L Duncan
Journal:  J Bacteriol       Date:  1973-02       Impact factor: 3.490

3.  Purification and biochemical properties of Clostridium perfringens type A enterotoxin.

Authors:  R L Stark; C L Duncan
Journal:  Infect Immun       Date:  1972-11       Impact factor: 3.441

4.  Quantitation of Clostridium perfringens type A enterotoxin by electroimmunodiffusion.

Authors:  C L Duncan; E B Somers
Journal:  Appl Microbiol       Date:  1972-11

5.  Isolation and purification of cortisol-binding immunoglobulin by affinity chromatography.

Authors:  A H Gijzen; P J Brombacher; H H Janssens; S H Deckers
Journal:  Clin Chim Acta       Date:  1975-01-20       Impact factor: 3.786

6.  Isolation by affinity chromatography of a precursor head protein (P23) of bacteriophage T4.

Authors:  M Yanagida
Journal:  J Mol Biol       Date:  1974-08-05       Impact factor: 5.469

7.  Biological characteristics of Clostridium perfringens type A enterotoxin.

Authors:  R L Stark; C L Duncan
Journal:  Infect Immun       Date:  1971-08       Impact factor: 3.441

8.  Improved medium for sporulation of Clostridium perfringens.

Authors:  C L Duncan; D H Strong
Journal:  Appl Microbiol       Date:  1968-01

9.  Ileal loop fluid accumulation and production of diarrhea in rabbits by cell-free products of Clostridium perfringens.

Authors:  C L Duncan; D H Strong
Journal:  J Bacteriol       Date:  1969-10       Impact factor: 3.490

10.  Sporulation and enterotoxin production by mutants of Clostridium perfringens.

Authors:  C L Duncan; D H Strong; M Sebald
Journal:  J Bacteriol       Date:  1972-04       Impact factor: 3.490

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  3 in total

1.  Preparative polyacrylamide gel electrophoresis purification of Clostridium perfringens enterotoxin.

Authors:  G L Enders; C L Duncan
Journal:  Infect Immun       Date:  1977-08       Impact factor: 3.441

2.  Purification by high performance liquid chromatography of Clostridium perfringens type A enterotoxin prepared from high toxin producers selected by a toxin-antitoxin halo.

Authors:  N Sugimoto; K Ozutsumi; M Matsuda
Journal:  Eur J Epidemiol       Date:  1985-06       Impact factor: 8.082

3.  Evidence for stable messenger ribonucleic acid during sporulation and enterotoxin synthesis by Clostridium perfringens type A.

Authors:  R G Labbe; C L Duncan
Journal:  J Bacteriol       Date:  1977-02       Impact factor: 3.490

  3 in total

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