食品科学 ›› 2017, Vol. 38 ›› Issue (2): 311-316.doi: 10.7506/spkx1002-6630-201702049

• 安全检测 • 上一篇    

微滴式数字聚合酶链式反应精准定量检测羊肉中掺杂猪肉

任君安,邓婷婷,黄文胜,葛毅强,陈 颖   

  1. 1.中国农业大学食品科学与营养工程学院,北京 100083;2.中国检验检疫科学研究院,北京 100176; 3.中国农村技术开发中心,北京 100045
  • 出版日期:2017-01-25 发布日期:2017-01-16
  • 基金资助:
    中国检验检疫科学研究院基本科研业务费专项(2014JK027);“十三五”国家重点研发计划重点专项(2016YFD0401104)

A Precise Quantitative Assay for Measuring Pork Incorporated into Mutton Products by Droplet Digital PCR

REN Jun’an, DENG Tingting, HUANG Wensheng, GE Yiqiang, CHEN Ying   

  1. 1. College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China; 2. Chinese Academy of Inspection and Quarantine, Beijing 100176, China; 3. China Rural Technology Development Center, Beijing 100045, China
  • Online:2017-01-25 Published:2017-01-16

摘要: 以羊和猪的单拷贝持家基因DNA复制蛋白A1为靶基因设计合成了适用于微滴式数字聚合酶链式反应的特异性引物和探针,通过理论推导获得了单位质量两种肉基因拷贝数之比的固定值,并进行了验证,据此将样品中羊肉和猪肉的拷贝数转换为相对质量分数,从而建立了羊肉中掺杂猪肉的精准定量检测方法。该方法可以很好地应用于羊肉中掺杂猪肉的含量检测,猪肉的最低定量限为1%,在5%~80%范围内绝对误差小于±1.30%,相对误差小于±10%,定量结果准确、重复性高,可以为肉类掺假的监管工作提供有力的技术参考。

 

关键词: 羊肉, 猪肉, 精准定量, 微滴式数字聚合酶链式反应

Abstract: The adulteration of meat products happened frequently in recent years, and authentication of meat products is necessary to protect consumers from an inferior product with a false description. Although at present, there are numerous qualitative methods for meat species identification, fewer quantitative detection methods have been reported. Herein, a droplet digital PCR method for the quantitative determination of pork incorporated in mutton products was developed. The single copy house-keeping gene encoding replication protein A1 (PRA1) was chosen as the target to design species-specific primers and probes for mutton and pig, respetively. Each assay was proved specific to the target species, respectively. The ratio constants between copy numbers and unit mass of pork and mutton were obtained by theoretical analysis and then verified by experiments. Consequently, the relative mass fractions of pork and mutton in the sample were measured based on the DNA copy numbers. The limit of quantitation (LOQ) of the method was confirmed to be 1%. The results showed that the absolute error was less than ±1.3%, and the relative error was less than ±10% in the range of pork proportion from 5% to 80%. The method developed in this paper was successfully applied to quantitate pork content incorporated into commercial mutton products and it may be useful for food administration laboratories to carry out meat species quantification in raw and processed foods.

Key words: mutton, pork, quantitative determination, droplet digital PCR (ddPCR)

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