Sakalar Ergün, Ergün Seyma Özçirak, Akar Emine
Department of Bioengineering, Faculty of Engineering, Canakkale Onsekiz Mart University, 17020 Canakkale, Turkey.
Korean J Food Sci Anim Resour. 2015;35(3):382-8. doi: 10.5851/kosfa.2015.35.3.382. Epub 2015 Jun 30.
A duplex real-time polymerase chain reaction (PCR) based assay for the detection of porcine and horse meat in sausages was designed by using EvaGreen fluorescent dye. Primers were selected from mitochondrial 12S rRNA and 16S rRNA genes which are powerful regions for identification of horse and porcine meat. DNA from reference samples and industrial products was successfully extracted using the GIDAGEN® Multi-Fast DNA Isolation Kit. Genomes were identified based on their specific melting peaks (Mp) which are 82.5℃ and 78℃ for horse and porcine, respectively. The assay used in this study allowed the detection of as little as 0.0001% level of horse meat and 0.001% level of porcine meat in the experimental admixtures. These findings indicate that EvaGreen based duplex real-time PCR is a potentially sensitive, reliable, rapid and accurate assay for the detection of meat species adulterated with porcine and horse meats.
利用EvaGreen荧光染料设计了一种基于双重实时聚合酶链反应(PCR)的检测香肠中猪肉和马肉的方法。引物选自线粒体12S rRNA和16S rRNA基因,这两个区域对马肉和猪肉的鉴定非常有效。使用GIDAGEN® Multi-Fast DNA分离试剂盒成功从参考样品和工业产品中提取了DNA。根据其特定的熔解峰(Mp)鉴定基因组,马肉和猪肉的熔解峰分别为82.5℃和78℃。本研究中使用的检测方法能够检测出实验混合物中低至0.0001%水平的马肉和0.001%水平的猪肉。这些结果表明,基于EvaGreen的双重实时PCR是一种潜在的灵敏、可靠、快速且准确的检测掺杂猪肉和马肉的肉类品种的方法。