Akiyama Hiroshi, Sugimoto Kazue, Matsumoto Misao, Isuzugawa Kazuto, Shibuya Masaaki, Goda Yukihiro, Toyoda Masatake
National Institute of Health Sciences: 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan.
Shokuhin Eiseigaku Zasshi. 2002 Feb;43(1):24-9. doi: 10.3358/shokueishi.43.24.
A detection method using polymerase chain reaction (PCR) was developed to detect the genetically modified (GM) potato (NewLeaf Plus potato; NL-P), which has not been authorized as safe in foods in Japan. The potato sucrose synthase gene was used as an internal control. The DNA from NL-P specifically provided an amplified band using PCR with a primer pair recognizing PLRV-rep gene. In addition, to prevent false-positive results in processed potato foods infected with PLRV, we designed a primer pair recognizing sequences derived from two organisms to detect specifically NL-P in processed potato. The PCR product obtained using the designed primer pair was specific for NL-P. The DNA introduced into NL-P could be detected from potato powder samples containing 0.05% NL-P. The proposed method was applied to the detection of NL-P in 25 processed potato foods. NL-P was detected in 3 snack products.
开发了一种使用聚合酶链反应(PCR)的检测方法,用于检测转基因(GM)马铃薯(NewLeaf Plus马铃薯;NL-P),该品种在日本尚未被批准作为安全食品。马铃薯蔗糖合酶基因用作内部对照。NL-P的DNA使用PCR和识别PLRV-rep基因的引物对特异性地产生扩增条带。此外,为防止感染PLRV的加工马铃薯食品出现假阳性结果,我们设计了一对识别来自两种生物序列的引物,以在加工马铃薯中特异性检测NL-P。使用设计的引物对获得的PCR产物对NL-P具有特异性。从含有0.05% NL-P的马铃薯粉样品中可以检测到导入NL-P的DNA。所提出的方法应用于25种加工马铃薯食品中NL-P的检测。在3种零食产品中检测到了NL-P。