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

机译:改进的多重PCR方法可同时检测产生生物胺的食用细菌

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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. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:这项研究描述了一种简单快速的多重PCR方法,以确定细菌产生组胺,酪胺和腐胺的能力。该测定法是基于针对乳酸菌设计的测定法的改进方法。这种改进的方法包括一对基于来自革兰氏阴性细菌的组氨酸脱羧酶序列的引物。在优化的条件下,该分析从革兰氏阳性细菌的组氨酸脱羧酶中提取了367bp的DNA片段,从革兰氏阴性细菌的组氨酸脱羧酶中提取了534bp的片段,从细菌酪氨酸脱羧酶得到了924bp的片段,细菌鸟氨酸脱羧酶。该方法已成功应用于几种生物胺生成细菌菌株,即使同一反应中包括了几种目标生物的DNA。这种简单的方法可以轻松地应用于食品控制实验室,以检测食品中潜在的生物胺生成细菌。 (c)2005年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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