Department of Genetics and Bioengineering, Faculty of Engineering, Fatih University, Büyükçekmece, 34500, Istanbul, Turkey,
Appl Biochem Biotechnol. 2013 Dec;171(7):1855-64. doi: 10.1007/s12010-013-0485-7. Epub 2013 Sep 6.
EvaGreen multiplex real-time polymerase chain reaction (EMRT-PCR) was designed for an assay that can join the advantages of multiplex PCR and real-time PCR to recognize animal genes more quickly in pet foods. EMRT-PCR based on melting temperatures discrimination by using EvaGreen fluorescence dye was developed for the analysis of pork and poultry in pet food. The method combines the use of poultry- and pork-specific primers that amplify small fragments of 12S rRNA and mitochondrial DNA genes. Appropriate mixtures of poultry and pork meat in reference samples were used to develop the assay. Gene yields of poultry and pork were represented in two melting peaks generated simultaneously at temperatures of 80.5 and 87.2 °C, respectively. Based upon the assay results, it has been concluded that EMRT-PCR assay might be an efficient tool for the verification of species origin in pet foods.
EvaGreen 多重实时聚合酶链反应 (EMRT-PCR) 设计用于一种检测方法,该方法可以结合多重 PCR 和实时 PCR 的优势,更快地识别宠物食品中的动物基因。基于 EvaGreen 荧光染料的熔解温度区分的 EMRT-PCR 是为分析宠物食品中的猪肉和家禽而开发的。该方法结合使用了禽类和猪肉特异性引物,扩增 12S rRNA 和线粒体 DNA 基因的小片段。在参考样本中使用适当比例的禽肉和猪肉来开发该检测方法。禽肉和猪肉的基因产量分别在 80.5°C 和 87.2°C 时同时产生的两个熔解峰中表示。根据检测结果,EMRT-PCR 检测方法可能是验证宠物食品中动物物种来源的有效工具。