Application of a qualitative and quantitative real-time polymerase chain reaction method for detecting genetically modified papaya line 55-1 in papaya products

被引:15
作者
Nakamura, Kosuke [1 ]
Akiyama, Hiroshi [1 ]
Takahashi, Yuki [1 ,2 ]
Kobayashi, Tomoko [1 ]
Noguchi, Akio [1 ]
Ohmori, Kiyomi [3 ]
Kasahara, Masaki [4 ]
Kitta, Kazumi [5 ]
Nakazawa, Hiroyuki [2 ]
Kondo, Kazunari [1 ]
Teshima, Reiko [1 ]
机构
[1] Natl Inst Hlth Sci, Setagaya Ku, Tokyo 1588501, Japan
[2] Hoshi Univ, Fac Pharmaceut Sci, Dept Analyt Chem, Shinagawa Ku, Tokyo 1428501, Japan
[3] Kanagawa Prefectural Inst Publ Hlth, Div Chem, Chigasaki, Kanagawa 2530087, Japan
[4] Food & Agr Mat Inspect Ctr, Chuo Ku, Saitama 3309731, Japan
[5] Natl Food Res Inst, Tsukuba, Ibaraki 3058642, Japan
关键词
Genetically modified organism; Genomic DNA; 55-1; Papaya; Real-time PCR; DETECTION SYSTEM;
D O I
10.1016/j.foodchem.2012.08.088
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Genetically modified (GM) papaya (Carica papaya L.) line 55-1 (55-1), which is resistant to papaya ringspot virus infection, has been marketed internationally. Many countries have mandatory labeling regulations for GM foods, and there is a need for specific methods for detecting 55-1. Here, an event- and construct-specific real-time polymerase chain reaction (PCR) method was developed for detecting 55-1 in papaya products. Quantitative detection was possible for fresh papaya fruit up to dilutions of 0.001% and 0.01% (weight per weight [w/w]) for homozygous SunUp and heterozygous Rainbow cultivars, respectively, in non-GM papaya. The limit of detection and quantification was as low as 250 copies of the haploid genome according to a standard reference plasmid. The method was applicable to qualitative detection of 55-1 in eight types of processed products (canned papaya, pickled papaya, dried fruit, papaya-leaf tea, jam, puree, juice, and frozen dessert) containing papaya as a main ingredient. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:895 / 901
页数:7
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