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用于同时检测产生物胺食品细菌的改进型多重聚合酶链反应方法

Improved multiplex-PCR method for the simultaneous detection of food bacteria producing biogenic amines.

作者信息

de Las Rivas Blanca, Marcobal Angela, Muñoz Rosario

机构信息

Departamento de Microbiología, Instituto de Fermentaciones Industriales, Juan de la Cierva 3, 28006 Madrid, Spain.

出版信息

FEMS Microbiol Lett. 2005 Mar 15;244(2):367-72. doi: 10.1016/j.femsle.2005.02.012.

Abstract

This study describes a simple and rapid multiplex-PCR method to determine the ability to produce histamine, tyramine and putrescine by bacteria. The assay is an improved method based on an assay designed for lactic acid bacteria. This improved method includes a pair of primers based on sequences from histidine decarboxylases from Gram-negative bacteria. Under the optimised conditions, the assay yielded a 367-bp DNA fragment from histidine decarboxylases of Gram-positive bacteria, 534-bp fragment from histidine decarboxylases of Gram-negative bacteria, 924-bp from bacterial tyrosine decarboxylases, and 1446-bp fragment from bacterial ornithine decarboxylases. The method was successfully applied to several biogenic amine-producing bacterial strains, even when DNAs of several target organisms were included in the same reaction. This simple method could be easily incorporated in food control laboratories to detect potentially biogenic amine-producing bacteria in foods.

摘要

本研究描述了一种简单快速的多重聚合酶链反应方法,用于测定细菌产生组胺、酪胺和腐胺的能力。该检测方法是基于一种针对乳酸菌设计的检测方法改进而来。这种改进方法包括一对基于革兰氏阴性菌组氨酸脱羧酶序列的引物。在优化条件下,该检测方法从革兰氏阳性菌组氨酸脱羧酶中产生了一个367 bp的DNA片段,从革兰氏阴性菌组氨酸脱羧酶中产生了534 bp的片段,从细菌酪氨酸脱羧酶中产生了924 bp的片段,从细菌鸟氨酸脱羧酶中产生了1446 bp的片段。该方法成功应用于几种产生物胺的细菌菌株,即使在同一反应中包含几种目标生物体的DNA时也是如此。这种简单的方法可以很容易地应用于食品控制实验室,以检测食品中潜在的产生物胺细菌。

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