利用线粒体细胞色素b的信息识别鸡肉加工中的假猪肉

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Mitochondrial Dna Part a Pub Date : 2017-11-01 DOI:10.1080/24701394.2016.1197220
H. Yacoub, M. A. Sadek
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引用次数: 24

摘要

本研究旨在通过一种可靠的方式,发现鸡肉加工肉类成分中的欺诈行为,保护消费者免受商业掺假和认证:对线粒体DNA细胞色素b基因保守片段进行直接扩增,并对某一细胞色素b进行物种特异性引物测定。结果报道,通过mtDNA细胞色素b基因保守片段的扩增,鸡肉加工肉被鉴定为鸡肉,而使用物种特异性引物后产生的片段大小不同,如下:鸡、山羊、牛、绵羊、猪和马的生肉分别为227、157、274、331、389和439 bp。结果表明,所有鸡肉产品的大小为227 bp。利用细胞色素b基因特异性引物,在鸡午餐和鸡汉堡等鸡肉产品中发现了猪肉掺假现象。这项研究代表了一种可靠的技术,可用于为识别零售市场上加工肉类中的商业掺假和替代品提供有前途的解决方案。
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Identification of fraud (with pig stuffs) in chicken-processed meat through information of mitochondrial cytochrome b
Abstract This study was conducted to find out the fraud in chicken-processed meat ingredients to protect consumers from commercial adulteration and authentication through a reliable way: direct amplification of conserved segment of cytochrome b gene of mitochondrial DNA, in addition, using species-specific primer assay for a certain cytochrome b. The results reported that chicken-processed meats were identified as a chicken meat based on amplification of conserved cytochrome b gene of mtDNA, while different fragments sizes were produced after the application of species-specific primer as follows: 227, 157, 274, 331, 389 and 439 bp for raw meat of chicken, goat, cattle, sheep, pig and horse, respectively. The results revealed that all chicken meat products are produced with 227 bp in size. While, an adulteration with pork stuffs was observed in some of the chicken meat products using a species-specific primer of cytochrome b gene, namely, chicken luncheon and chicken burger. This study represents a reliable technique that could be used to provide a promising solution for identifying the commercial adulteration and substitutions in processed meat in retail markets.
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来源期刊
Mitochondrial Dna Part a
Mitochondrial Dna Part a Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.00
自引率
0.00%
发文量
6
期刊介绍: Mitochondrial DNA Part A publishes original high-quality manuscripts on physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism, and/or interactions. Manuscripts on cytosolic and extracellular mtDNA, and on dysfunction caused by alterations in mtDNA integrity as well as methodological papers detailing novel approaches for mtDNA manipulation in vitro and in vivo are welcome. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The Journal also considers manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences, as well as papers that discuss the utility of mitochondrial DNA information in medical studies and in human evolutionary biology.
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