Real-time PCR for quantitative meat species testing

被引:104
作者
Sawyer, J [1 ]
Wood, C [1 ]
Shanahan, D [1 ]
Gout, S [1 ]
McDowell, D [1 ]
机构
[1] Lab Govt Chemist, Dept Life Sci Res, Teddington TW11 0LY, Middx, England
关键词
authenticity; quantification; real-time PCR;
D O I
10.1016/S0956-7135(02)00148-2
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A method for quantitative meat speciation is described which combines the use of real-time PCR with species specific and 'universal' primers to measure individual species content and total meat content respectively. A comparison of the cycle number at which universal and species specific PCR products are first detected, in combination with the use of reference standards of known species content, is used as the basis for determining the percentage of a given species in a mixed sample. Importantly, the use of universal primers allows differences in DNA quality between samples and reference standards to be taken into account, while the use of real-time PCR allows measurement at an early stage in the PCR process which is inherently more accurate than the end point analysis associated with gel-based systems. This paper describes the quantification of beef in mixed samples to illustrate the principle of this approach. (C) 2003 Published by Elsevier Ltd.
引用
收藏
页码:579 / 583
页数:5
相关论文
共 20 条
[1]   COMPLETE SEQUENCE OF BOVINE MITOCHONDRIAL-DNA - CONSERVED FEATURES OF THE MAMMALIAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
DEBRUIJN, MHL ;
COULSON, AR ;
EPERON, IC ;
SANGER, F ;
YOUNG, IG .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 156 (04) :683-717
[2]  
Barai B. K., 1992, Trends in Food Science & Technology, V3, P69, DOI 10.1016/0924-2244(92)90133-H
[3]  
BARTLETT SE, 1992, BIOTECHNIQUES, V12, P408
[4]   SEQUENCE AND GENE ORGANIZATION OF THE CHICKEN MITOCHONDRIAL GENOME - A NOVEL GENE ORDER IN HIGHER VERTEBRATES [J].
DESJARDINS, P ;
MORAIS, R .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 212 (04) :599-634
[5]  
GHIVIZZANI SC, 1993, J MOL EVOL, V37, P36, DOI 10.1007/BF00170460
[6]   Real time quantitative PCR [J].
Heid, CA ;
Stevens, J ;
Livak, KJ ;
Williams, PM .
GENOME RESEARCH, 1996, 6 (10) :986-994
[7]   SIMULTANEOUS AMPLIFICATION AND DETECTION OF SPECIFIC DNA-SEQUENCES [J].
HIGUCHI, R ;
DOLLINGER, G ;
WALSH, PS ;
GRIFFITH, R .
BIO-TECHNOLOGY, 1992, 10 (04) :413-417
[8]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030
[9]  
Hunt DJ, 1997, FOOD CHEM, V60, P437, DOI 10.1016/S0308-8146(96)00364-0
[10]   Species identification in meat by using PCR-generated satellite probes [J].
Janssen, FW ;
Hägele, GH ;
Buntjer, JB ;
Lenstra, JA .
JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 1998, 21 (03) :115-120