Oguchi Taichi, Onishi Mari, Mano Junichi, Akiyama Hiroshi, Teshima Reiko, Futo Satoshi, Furui Satoshi, Kitta Kazumi
GMO Analytical Evaluation Laboratory, National Food Research Institute, National Agriculture and Food Research Organization, Tsukuba, Ibaraki 305-8642, Japan.
Shokuhin Eiseigaku Zasshi. 2010;51(3):92-100. doi: 10.3358/shokueishi.51.92.
A novel multiplex PCR method was developed for simultaneous event-specific detection of four events of GM maize, i.e., DAS-59122-7, MIR604, MON88017, and MON863. The single laboratory examination of analytical performance using simulated DNA mixtures containing GM DNA at various concentrations in non-GM DNA suggested that the limits of detection (LOD) of the multiplex PCR method were 0.16% for MON863, MIR604, and MON88017, and 0.078% for DAS-59122-7. We previously developed a nonaplex (9plex) PCR method for eight events of GM maize, i.e., Bt11, Bt176, GA21, MON810, MON863, NK603, T25, and TC1507. Together with the nonaplex PCR method, the newly developed method enabled the detection and identification of eleven GM maize events that are frequently included in commercial GM seed used in Japan. In addition, this combinational analysis may be useful for the identification of combined event products of GM maize.
开发了一种新型多重PCR方法,用于同时对转基因玉米的四个事件进行事件特异性检测,即DAS-59122-7、MIR604、MON88017和MON863。在非转基因DNA中使用含有不同浓度转基因DNA的模拟DNA混合物进行的单实验室分析性能检测表明,多重PCR方法对MON863、MIR604和MON88017的检测限(LOD)为0.16%,对DAS-59122-7的检测限为0.078%。我们之前开发了一种用于八个转基因玉米事件的九重PCR方法,即Bt11、Bt176、GA21、MON810、MON863、NK603、T25和TC1507。与九重PCR方法一起,新开发的方法能够检测和鉴定日本商业转基因种子中经常包含的11个转基因玉米事件。此外,这种组合分析可能有助于鉴定转基因玉米的复合事件产品。