Simple and fast multiplex PCR method for detection of species origin in meat products

被引:26
作者
Izadpanah, Mehrnaz [1 ,2 ]
Mohebali, Nazanin [1 ]
Gorji, Zahra Elyasi [1 ]
Farzaneh, Parvaneh [1 ]
Vakhshiteh, Faezeh [1 ]
Fazeli, Seyed Abolhassan Shahzadeh [1 ,3 ]
机构
[1] Iranian Biol Resource Ctr IBRC, ACECR, Human & Anim Cell Bank, Tehran, Iran
[2] Univ Tehran Med Sci, Sch Adv Technol Med, Tehran, Iran
[3] Univ Sci & Culture, Fac Basic Sci & Adv Technol Biol, Dept Mol & Cellular Biol, Tehran, Iran
来源
JOURNAL OF FOOD SCIENCE AND TECHNOLOGY-MYSORE | 2018年 / 55卷 / 02期
关键词
Species identification; Mitochondrial Cytochrome C Oxidase subunit I (COX1); Multiplex PCR; IDENTIFICATION; ASSAY; DNA; AUTHENTICATION; CHICKEN; PORK;
D O I
10.1007/s13197-017-2980-2
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Identification of animal species is one of the major concerns in food regulatory control and quality assurance system. Different approaches have been used for species identification in animal origin of feedstuff. This study aimed to develop a multiplex PCR approach to detect the origin of meat and meat products. Specific primers were designed based on the conserved region of mitochondrial Cytochrome C Oxidase subunit I (COX1) gene. This method could successfully distinguish the origin of the pig, camel, sheep, donkey, goat, cow, and chicken in one single reaction. Since PCR products derived from each species represent unique molecular weight, the amplified products could be identified by electrophoresis and analyzed based on their size. Due to the synchronized amplification of segments within a single PCR reaction, multiplex PCR is considered to be a simple, fast, and inexpensive technique that can be applied for identification of meat products in food industries. Nowadays, this technique has been considered as a practical method to identify the species origin, which could further applied for animal feedstuffs identification.
引用
收藏
页码:698 / 703
页数:6
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