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Real-time PCR based on single-copy housekeeping genes for quantitative detection of goat meat adulteration with pork

机译:基于单拷贝看家基因的实时PCR定量检测山羊肉掺假猪肉

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摘要

Adulteration of goat meat with cheaper meat such as pork has been frequently found. Conventional PCR methods to distinguish goat meat from adulteration are qualitative, which easily produce false-positive results due to contamination but not adulteration. To address this problem, real-time PCR based on single-copy housekeeping genes encoding replication protein A1 was developed for goat meat and pork. By calculating the Ct ratio of goat meat/pork, the goat meat content in a suspected adulteration could be deduced by a good linear correlation (R-2 = 0.9868) in a range from 5% to 80%. Analysis of the simulated samples of goat meat showed high accuracy with recoveries of 104.91% and 105.00% for the goat meat contents of 40% and 60%, respectively, and coefficient of variations were as low as 9.24% and 9.09%. Thus, the developed assay supplied a useful tool for food regulation authorities to achieve quantitative authentication of goat meat.
机译:经常发现山羊肉与便宜的肉类如猪肉掺假。常规PCR方法可将山羊肉与掺假区别开来,是定性的,由于污染而不掺假,很容易产生假阳性结果。为了解决这个问题,针对山羊肉和猪肉开发了基于单拷贝管家基因的实时PCR,该基因编码复制蛋白A1。通过计算山羊肉/猪肉的Ct比,可以通过在5%到80%范围内的良好线性相关性(R-2 = 0.9868)来推断可疑掺假中山羊肉的含量。对山羊肉模拟样品的分析显示出较高的准确性,山羊肉含量为40%和60%时,回收率分别为104.91%和105.00%,变异系数低至9.24%和9.09%。因此,开发的检测方法为食品监管部门提供了一种对山羊肉进行定量认证的有用工具。

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