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通过酶免疫测定法直接在膜滤器上显示产肠毒素菌落来快速计数食品中的金黄色葡萄球菌。

Rapid enumeration of Staphylococcus aureus in foods by direct demonstration of enterotoxigenic colonies on membrane filters by enzyme immunoassay.

作者信息

Peterkin P I, Sharpe A N

出版信息

Appl Environ Microbiol. 1984 May;47(5):1047-53. doi: 10.1128/aem.47.5.1047-1053.1984.

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.

摘要

基于酶联免疫吸附测定法,已设计出一种简便方法,可直接证明在膜滤器上生长24小时的金黄色葡萄球菌菌落产生的肠毒素B。通过将辣根过氧化物酶直接与蛋白A偶联,利用免疫球蛋白G与蛋白A结合导致的假阳性反应问题,蛋白A随后介导抗毒素的标记。该检测需要3小时完成,并在产生肠毒素B的菌落部位产生紫色染色,从而能够在27小时内直接计数食品中经确认的金黄色葡萄球菌。该方法应适用于金黄色葡萄球菌的其他肠毒素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77f/240052/d87a368a4b2d/aem00162-0170-a.jpg

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