Department of Functional Biology, University of Oviedo. C/Julian Claveria s/n, E-33006 Oviedo, Spain.
J Sci Food Agric. 2013 Jan;93(2):354-61. doi: 10.1002/jsfa.5766. Epub 2012 Jun 27.
There are many DNA-based systems for detecting animal species present in food and food products, applicable for food quality control and authentication. However, most (if not all) methods require more than one pair of primers and cannot be applied over a wide taxonomic range, e.g. identifying vertebrates and invertebrates with the same primers and protocols.
A pair of primers is described here that allows in a single polymerase chain reaction the identification of animal species in food and processed (precooked, canned or smoked) food products over a wide taxonomic range.
These primers permit the identification of most animal taxa employed in human nutrition, from invertebrates such as molluscs to higher vertebrates, distinguishing between species of the same genus. The short fragment amplified within the 16S rDNA exhibits phylogenetic value and could be considered universal based on the wide taxonomic range assayed. The primers are easy to use and accessible for laboratories with a modest budget, as well as being valuable for consumer information and to reveal food fraud.
有许多基于 DNA 的系统可用于检测食品和食品中存在的动物物种,适用于食品质量控制和认证。然而,大多数(如果不是全部)方法需要不止一对引物,并且不能应用于广泛的分类范围,例如使用相同的引物和方案识别脊椎动物和无脊椎动物。
本文描述了一对引物,允许在单个聚合酶链反应中鉴定食品和加工(预煮、罐装或熏制)食品中的动物物种,涵盖广泛的分类范围。
这些引物允许鉴定人类营养中使用的大多数动物分类群,从无脊椎动物(如软体动物)到高等脊椎动物,并区分同一属的物种。在 16S rDNA 内扩增的短片段具有系统发育价值,并且可以根据所检测的广泛分类范围被认为是通用的。这些引物易于使用,适合预算有限的实验室使用,并且对消费者信息和揭示食品欺诈具有重要价值。