Kitpipit Thitika, Sittichan Kuangtiwa, Thanakiatkrai Phuvadol
Forensic Science Program, Department of Applied Science, Faculty of Science, Prince of Songkla University, 90112, Thailand.
Forensic Science Program, Department of Applied Science, Faculty of Science, Prince of Songkla University, 90112, Thailand.
Food Chem. 2014 Nov 15;163:77-82. doi: 10.1016/j.foodchem.2014.04.062. Epub 2014 Apr 24.
This is the first time that direct PCR - DNA amplification without prior DNA extraction - was successfully developed and fully validated for rapid and economical simultaneous identification of six commonly consumed meat species. To achieve this, six species-specific primers were selected from previous reports and newly designed from the mitochondrial cytochrome b (cyt b), cytochrome oxidase I (COI), and 12s rRNA gene. The assay generated PCR products of 100, 119, 133, 155, 253, and 311 bp for pork, lamb/mutton, chicken, ostrich meat, horsemeat and beef, respectively. Validation showed that the assay is robust, rapid, economical, reproducible, specific, and sensitive down to 12,500 mitochondrial copy (equating to seven fg). It could be used with a variety of raw meats and products, including highly degraded and processed food samples. This proposed method will be greatly beneficial to the consumers, food industry, and law enforcement.
这是首次成功开发并充分验证了无需预先提取DNA的直接PCR - DNA扩增方法,用于快速且经济地同时鉴定六种常见消费肉类品种。为此,从先前的报告中选择了六种物种特异性引物,并根据线粒体细胞色素b(cyt b)、细胞色素氧化酶I(COI)和12s rRNA基因新设计了引物。该检测方法分别针对猪肉、羊肉、鸡肉、鸵鸟肉、马肉和牛肉生成了100、119、133、155、253和311 bp的PCR产物。验证表明,该检测方法稳健、快速、经济、可重复、特异,灵敏度低至12,500个线粒体拷贝(相当于7 fg)。它可用于各种生肉和产品,包括高度降解和加工的食品样本。这种提议的方法将对消费者、食品行业和执法部门大有裨益。