AI Article Synopsis

  • The study focused on detecting contamination of processed vegetable foods with genetically modified (GM) tomatoes using qualitative PCR methods.
  • DNA fragments linked to the cauliflower mosaic virus 35S promoter (P35S) and kanamycin resistance gene (NPTII) were found in vegetable juice samples, likely from virus-infected Brassica species and soil bacteria.
  • However, no specific GM tomato sequences were amplified from the juice, indicating that the qualitative PCR method is effective for checking for GM tomato contamination.

Article Abstract

The contamination of processed vegetable foods with genetically modified tomatoes was investigated by the use of qualitative PCR methods to detect the cauliflower mosaic virus 35S promoter (P35S) and the kanamycin resistance gene (NPTII). DNA fragments of P35S and NPTII were detected in vegetable juice samples, possibly due to contamination with the genomes of cauliflower mosaic virus infecting juice ingredients of Brassica species and soil bacteria, respectively. Therefore, to detect the transformation construct sequences of GM tomatoes, primer pairs were designed for qualitative PCR to specifically detect the border region between P35S and NPTII, and the border region between nopaline synthase gene promoter and NPTII. No amplification of the targeted sequences was observed using genomic DNA purified from the juice ingredients. The developed qualitative PCR method is considered to be a reliable tool to check contamination of products with GM tomatoes.

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Source
http://dx.doi.org/10.3358/shokueishi.55.247DOI Listing

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