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  • 1
    ISSN: 1438-2385
    Keywords: Soya protein concentrates ; Meat products ; Nested PCR ; ELISA ; Food authenticity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract A new method for the specific and sensitive detection of soya (Glycine max) in processed meat products has been developed using polymerase chain reaction (PCR) technology. The presence of soya deoxyribonucleic acid (DNA) from several soya protein concentrates was determined with two pairs of specific oligonucleotides yielding a 414-bp (bp=base pair) fragment and an internal 118-bp fragment amplified from the soya lectinLe1 gene. The test detected DNA from textured soya protein concentrates in meat products at a level of 1% and was confirmed by a commercially available enzyme-linked immunosorbent assay (ELISA).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Zeitschrift für Lebensmittel-Untersuchung und -Forschung 207 (1998), S. 81-90 
    ISSN: 1431-4630
    Keywords: Key words Genetically modified organisms ; Food ; Polymerase chain reaction ; Tofu ; Lecithin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract  Deoxyribonucleic acids (DNA) and ribonucleic acids (RNA) as normal compounds of many foodstuffs have so far been of minor interest with respect to human and animal nutrition. Through the approval of various genetically modified crops in the United States and Europe in recent years, these nucleic acids (NA) have become an important tool in food analysis. The reason for this is that in most cases the discrimination between a genetically modified foodstuff and an unmodified one can best be achieved directly at the DNA level by means of proving the presence or absence of the introduced gene(s). So far, the various methods that can be used to purify DNA for such types of analysis have rarely been compared in a comprehensive manner. In this work the effects of nine different extraction methods on yield and quality of previously purified high-molecular-weight DNA from soya beans and of total NA from tofu, soya flour and lecithin have been tested. Quantification was accomplished using UV absorption at 260 nm and quality assessment of the DNA was done by polymerase chain reaction (PCR) with the soya bean-specific lectin 1 system. Using this approach we assessed the limits of DNA amplification for each food sample extracted using different extraction protocols. It was demonstrated that extraction methods using NA-binding resins like Wizard or DNeasy resulted in comparatively low yields. However, the DNA extracted with these methods is of high quality and suitable for downstream processing like PCR. Simpler and faster methods resulted in relatively high yields of NA but of relatively poor quality. Inhibition of PCR was observed due to one of the buffers used during NA extraction. Finally, the different extraction methods used in this study were compared with respect to the costs and the time needed to perform the extractions.
    Type of Medium: Electronic Resource
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