Comparison of simplex and duplex real-time PCR for the quantification of GMO in maize and soybean

被引:46
作者
Alary, R [1 ]
Serin, A [1 ]
Maury, D [1 ]
Ben Jouira, H [1 ]
Sirven, JP [1 ]
Gautier, MF [1 ]
Joudrier, P [1 ]
机构
[1] INRA, Unite Biochim & Biol Mol Cereales, F-34060 Montpellier 01, France
关键词
GMO labelling; GMO quantification; real-time PCR; maize; soybean;
D O I
10.1016/S0956-7135(02)00015-4
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
This paper focuses on the determination of the GMO content of maize and soybean samples Using real-time PCR, comparing simplex and duplex PCR. The total DNA content of samples was determined by amplifying part of a maize gene encoding a lipid transfer protein, or part of a soybean lectin gene. The transgenic DNA was quantified by amplifying part of the CaMV 35S promoter. The importance of preparation and conservation of standards as well Lis the relevance of DNA extraction protocol on the variability of results are discussed. For the determination of low GMO content, limitation in the number of copies of the target gene to be amplified is considered. For samples with a theoretical GMO content of corresponding to the legal threshold for labelling, the value determined by duplex real-time PCR ranged from 0.85% to 1.20%. Both real-time simplex and duplex PCRs allowed identification of GMO free samples without ambiguity. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:235 / 244
页数:10
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