Bellagamba F, Moretti V M, Comincini S, Valfrè F
Istituto di Zootecnica, Facoltà di Medicina Veterinaria, Università degli Studi di Milano, Via Trentacoste 2, 20134 Milano, Italy.
J Agric Food Chem. 2001 Aug;49(8):3775-81. doi: 10.1021/jf0010329.
Restriction site analysis of Polymerase Chain Reaction (PCR) products of cytochrome b mitochondrial DNA was applied to identify species in meat meal and animal feedstuffs. PCR was used to amplify a variable region of cytochrome b mitochondrial DNA gene. Species differentiation was determined by digestion of the obtained 359 bp amplicon with restriction enzymes, which generated species-specific electrophoresis patterns; the sequencing of PCR products was used as confirming analysis. PCR-RFLP analysis revealed the presence of meat meal in animal feedstuffs and distinguished species of interest. The results supported the application of the method in control measures which should be adopted for meat-meal-based animal feed, as suggested by EU law. As a technical improvement, to simplify the analysis, the number of enzymes presented in this study for the detection of different species was smaller than others described in the literature; discrimination between ruminant and nonruminant species and between mammalian and poultry species was possible with few digestions.
应用细胞色素b线粒体DNA的聚合酶链反应(PCR)产物的限制性酶切位点分析来鉴定肉骨粉和动物饲料中的物种。PCR用于扩增细胞色素b线粒体DNA基因的一个可变区域。通过用限制性酶消化获得的359 bp扩增子来确定物种分化,这产生了物种特异性的电泳图谱;PCR产物的测序用作确认分析。PCR-RFLP分析揭示了动物饲料中肉骨粉的存在并区分了感兴趣的物种。结果支持了该方法在欧盟法律建议的基于肉骨粉的动物饲料应采取的控制措施中的应用。作为一项技术改进,为了简化分析,本研究中用于检测不同物种的酶的数量比文献中描述的其他方法要少;通过少量酶切就可以区分反刍动物和非反刍动物物种以及哺乳动物和家禽物种。