College of Life Sciences, China Jiliang University, Hangzhou 310018, China.
Taizhou Food and Drug Inspection and Research Institute, Taizhou 318000, China.
J Agric Food Chem. 2024 May 22;72(20):11640-11651. doi: 10.1021/acs.jafc.4c01294. Epub 2024 May 9.
Milk and dairy products represent important sources of nutrition in our daily lives. The identification of species within dairy products holds importance for monitoring food adulteration and ensuring traceability. This study presented a method that integrated double-tube and duplex real-time polymerase chain reaction (PCR) with multiplex TaqMan probes to enable the high-throughput detection of animal-derived ingredients in milk and dairy products. The detection system utilized one pair of universal primers, two pairs of specific primers, and eight animal-derived specific probes for cow, buffalo, goat, sheep, camel, yak, horse, and donkey. These components were optimized within a double-tube and four-probe PCR multiplex system. The developed double-tube detection system could simultaneously identify the above eight targets with a detection limit of 10-0.1 pg/μL. Validation using simulated adulterated milk samples demonstrated a detection limit of 0.1%. The primary advantage of this method lies in the simplification of the multiplex quantitative real-time PCR (qPCR) system through the use of universal primers. This method provides an efficient approach for detecting ingredients in dairy products, providing powerful technical support for market supervision.
牛奶和乳制品是我们日常生活中重要的营养来源。鉴定乳制品中的物种对于监测食品掺假和确保可追溯性非常重要。本研究提出了一种方法,该方法将双管和双管实时聚合酶链反应(PCR)与多重 TaqMan 探针相结合,实现了对牛奶和乳制品中动物源性成分的高通量检测。该检测系统使用一对通用引物、两对特异性引物和八对牛、水牛、山羊、绵羊、骆驼、牦牛、马和驴的特异性探针。这些组件在双管和四探针 PCR 多重系统中进行了优化。开发的双管检测系统能够同时识别上述 8 个目标,检测限为 10-0.1 pg/μL。使用模拟掺假牛奶样品进行的验证表明检测限为 0.1%。该方法的主要优点在于通过使用通用引物简化了多重实时定量 PCR(qPCR)系统。该方法为检测乳制品中的成分提供了一种有效的方法,为市场监管提供了有力的技术支持。