Detection of Chicken and Turkey Meat in Meat Mixtures by Using Real-Time PCR Assays

被引:85
作者
Kesmen, Zulal [1 ]
Yetiman, Ahmet E. [1 ]
Sahin, Fikrettin [2 ]
Yetim, Hasan [1 ]
机构
[1] Erciyes Univ, Dept Food Engn, Fac Engn, TR-38039 Kayseri, Turkey
[2] Yeditepe Univ, Dept Bioengn, Coll Engn, TR-34755 Istanbul, Turkey
关键词
conventional PCR chicken; real-time PCR; species identification; TaqMan probe; turkey; POLYMERASE-CHAIN-REACTION; MITOCHONDRIAL-DNA; SPECIES IDENTIFICATION; PRODUCTS; PORK; FOOD; AMPLIFICATION; ORIGIN; GENE; BEEF;
D O I
10.1111/j.1750-3841.2011.02536.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In this study, TaqMan-based real-time Polymerase Chain Reaction (PCR) techniques were developed for the detection of chicken and turkey meat in raw and heat-treated meat mixtures. Primers and TaqMan probe sets were designed to amplify 86 bp and 136 bp fragments for the chicken and turkey species, respectively, on the mitochondrial NADH dehydrogenase subunit 2 gene. In the results, it was possible to detect each species at the level of 0.1 pg template DNA with the TaqMan probe technique without any cross-reactivity with nontarget species (bovine, ovine, donkey, pork, and horse) while the detection level was 1 pg template DNA using conventional PCR. The TaqMan probe assays used in this study allowed the detection of as little as 0.001% level of both species in the experimental meat mixtures, prepared by mixing chicken and turkey meat with beef at different levels (0.001% to 10%). In conclusion, TaqMan probe assays developed in this research are promising tools in the specific identification and sensitive quantification of meat species even in the case of heat-treated meat products, and suitable for a rapid, automated, and routine analysis.
引用
收藏
页码:C167 / C173
页数:7
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