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利用 TaqMan 实时 PCR 检测工业饲料中的禁用反刍动物源性物质。

Detection of banned ruminant-derived material in industrial feedstuffs by TaqMan real-time PCR Assay.

机构信息

Departamento de Nutrición, Bromatología y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Complutense de Madrid, 28040 Madrid, Spain.

出版信息

J Food Prot. 2011 Aug;74(8):1300-8. doi: 10.4315/0362-028X.JFP-11-029.

Abstract

A ruminant-specific real-time PCR system was designed and applied for the detection of processed animal protein from ruminants in industrial feedstuffs. The assay includes a primer pair and a TaqMan probe selectively targeting mitochondrial 16S rRNA gene sequences from the ruminant group and another primer-probe set based on the eukaryotic nuclear 18S rRNA gene (positive amplification control). Both ruminant and eukaryotic PCR systems generated short PCR amplicons of 79 and 77 bp, respectively. To evaluate the suitability of the real-time PCR assay for the detection of banned by-products of ruminant origin, 126 feed samples subjected to rendering under current European legislation regulations were analyzed. The assay achieved 100% success in classifying the samples as positive or negative in terms of qualitative ruminant composition, with a detection limit of 0.1%. The quantitative ability of the assay is however restricted by variations in the composition and treatment of the feeds, which affect the amount and quality of amplifiable DNA.

摘要

设计了一种反刍动物特异性实时 PCR 系统,用于检测工业饲料中来源于反刍动物的加工动物蛋白。该检测方法包括一对引物和 TaqMan 探针,它们特异性地针对来自反刍动物群的线粒体 16S rRNA 基因序列,以及另一组基于真核核 18S rRNA 基因的引物-探针(阳性扩增对照)。反刍动物和真核生物 PCR 系统分别产生 79bp 和 77bp 的短 PCR 扩增子。为了评估实时 PCR 检测方法对检测禁止的反刍动物源性副产品的适用性,分析了 126 种根据当前欧洲法规进行炼制的饲料样品。该检测方法在定性反刍动物组成方面,将样品分类为阳性或阴性的成功率达到 100%,检测限为 0.1%。然而,该检测方法的定量能力受到饲料成分和处理变化的限制,这些变化会影响可扩增 DNA 的数量和质量。

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