多重PCR检测猪肉以保证肉类加工产品的清真性

M. Indriati, E. Yuniarsih
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引用次数: 2

摘要

清真食品的参数之一是从基本配料、添加剂和生产过程中必须不含猪肉。本研究的目的是确保在pangdeglang摄政区传统市场的加工肉制品(肉丸和香肠)中是否存在猪肉的清真状态。多重聚合酶链反应(PCR)是一种利用多个引物在一次反应中扩增多个目标序列的PCR技术。通常用作动物或肉类类型标记的基因包括细胞色素b (cyt b), cyt b序列变异的存在使得这些基因被广泛用作区分不同类型动物材料的标记。结果表明,cyt b基因在两种家畜DNA混合物中不同片段长度的牛肉和猪肉的DNA扩增中一次反应成功,根据不同片段长度的不同,形成了两条不同长度的DNA条带。从研究结果来看,牛肉和猪肉的控制有两个片段,牛肉为274 bp,猪肉为389 bp。对肉丸样本的多重聚合酶链式反应测试显示,肉丸含牛肉DNA呈100%阳性,而含猪肉DNA为0%。在对香肠产品的检测中,有一个品牌的香肠的DNA扩增结果为398pb,这意味着该产品含有猪肉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiplex PCR Method of Detecting Pork to Guarantee Halal Status in Meat Processed Products
One of the halal parameters of food is must be free from pork among from the basic ingredients, additives and the manufacturing process. The aim of this study was ensure the halal status in the form of presence or absence of pork in processed meat product (meatballs and sausages) in traditional markets in Pandeglang Regency. PCR multiplex was a PCR technique that used several primers together in one reaction to amplify several target sequence. The genes often used as markers of animal or meat types include cytochrome b (cyt b), the existence of sequence variations in cyt b causes these genes are widely used as markers to distinguish material from different types of animals. The results showed that the cyt b gene proved successful in amplified DNA from beef and pork with different fragment lengths in the DNA mix of the 2 types of livestock in one reaction so that 2 DNA bands formed with different lengths according to the length of the fragment from each animal. From the results of research showed beef and pork control there was two fragments such as 274 bp for beef and 389 bp for pork. Multiplex PCR testing on meatball samples showed that the meatballs were tested 100% positive containing beef and 0% containing pork DNA. While testing on sausage products, there were one sausage brand that showed the results of DNA amplification of 398pb, which means the product was positive containing pork.
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