Abstract
Based on enzyme-linked immunosorbent assay, a convenient method has been devised for the direct demonstration of enterotoxin B production by Staphylococcus aureus colonies grown for 24 h on membrane filters. The problem of false-positive reactions due to binding of immunoglobulin G to protein A was turned to advantage by conjugating horseradish peroxidase directly to protein A, which then mediated the labeling of the antitoxin. The test requires 3 h to complete and yields a purple stain at the site of enterotoxin B-producing colonies, thus allowing direct enumeration of confirmed S. aureus in foods within 27 h. The method should be applicable to other enterotoxins of S. aureus.
MeSH Terms
Binding Sites
Enterotoxins/analysis,biosynthesis,metabolism
Enzyme-Linked Immunosorbent Assay
Food Microbiology
Immunoglobulin G/metabolism
Methods
Staphylococcal Protein A/metabolism
Staphylococcus aureus/metabolism
Chemicals
Enterotoxins
Immunoglobulin G
Staphylococcal Protein A
enterotoxin B, staphylococcal
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Peterkin P I
Sharpe A N
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15 references, click to expand
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