New Qualitative Detection Methods of Genetically Modified Potatoes
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- Watanabe Takahiro
- National Institute of Health Sciences, Japan
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- Kuribara Hideo
- National Food Research Institute, Japan
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- Mishima Takashi
- Japan Food Research Laboratories
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- Kikuchi Hiroyuki
- National Institute of Health Sciences, Japan
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- Kodama Takashi
- National Food Research Institute, Japan
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- Futo Satoshi
- FASMAC Co., Ltd.
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- Kasama Kikuko
- Japan Association of Prefectual and Municipal Public Health Institutes
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- Toyota Akie
- Japan Association of Prefectual and Municipal Public Health Institutes
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- Nouno Masanori
- Center for Inspection of Imported Foods and Infectious Diseases Yokohama Quarantine Station
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- Saita Ayako
- Center for Inspection of Imported Foods and Infectious Diseases Yokohama Quarantine Station
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- Takahashi Kunihiko
- Japan Association of Prefectual and Municipal Public Health Institutes
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- Hino Akihiro
- National Food Research Institute, Japan
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- Akiyama Hiroshi
- National Institute of Health Sciences, Japan
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- Maitani Tamio
- National Institute of Health Sciences, Japan
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説明
In Japan, 8 lines of genetically modified (GM) potato (2 lines of NewLeaf® potato; NL, 3 lines of NewLeaf Plus® potato; NLP, and 3 lines of NewLeaf Y® potato; NLY) have already been authorized as safe for use in foods and feeds. We have developed polymerase chain reaction (PCR) methods for the qualitative detection of the GM potatoes for the screening and the identification of NL, NLP and NLY. The gene encoding uridine diphosphate (UDP)-glucose pyrophosphorylase (UGPase) was used as a taxon specific gene. We designed the primer pair to detect the cryIIIA genes as a screening method for GM potatoes because the gene should be inserted in all 8 lines of the GM potatoes. For identification of NL, NLP and NLY, we further designed three specific primer pairs for the different recombinant DNAs (r-DNA) specifically introduced into NL, NLP, or NLY. In addition, to identify the 3 lines of NLY that have been introduced with the same r-DNA, the three line-specific primer pairs for the border sequence between the r-DNA and genomic DNA of NLY 3 lines were designed. Six lines of GM potato used as the test material were specifically identified using the each primer pair under the same PCR condition. The detection limits of all the GM potatoes should be approximately 0.1%. Furthermore, the specificity and reproducibility of the methods were confirmed in a six-laboratory collaborative study.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 27 (9), 1333-1339, 2004
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679602830720
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- NII論文ID
- 110003608972
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- NII書誌ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 7056234
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- PubMed
- 15340215
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
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- 使用不可