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Qualitative and quantitative assessment of genetically modified soy in enteral nutrition formulas by polymerase chain reaction based methods

机译:基于聚合酶链反应的方法对肠内营养配方食品中转基因大豆的定性和定量评估

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OBJECTIVE: The aim of this work was to investigate the occurrence of Roundup Ready soybean in enteral nutrition formulas sold in Brazil. METHODS: A duplex Polymerase Chain Reaction based on the amplification of the lectin gene and the construction of the recombinant deoxyribonucleic acid of transgenic glyphosate-tolerant soybean (35S promoter and chloroplast transit peptide gene) was performed in order to analyze the deoxyribonucleic acid obtained from nine soy protein isolate-containing formulas. RESULTS: Despite the highly processed nature of the food matrices, amplifiable deoxyribonucleic acid templates were obtained from all tested samples, as judged by the amplification of the lectin gene sequence. However, amplicons relative to the presence of Roundup Ready soybean were restricted to one of the nine enteral nutrition formulas analyzed as well as to the soybean reference powder, as expected. Quantitative analysis of the genetically modified formula by real-time Polymerase Chain Reaction showed a content of approximately 0.3% (w/w) of recombinant deoxyribonucleic acid from the Roundup Ready soybean. CONCLUSION: The results show that one of the formulas contained genetically modified soy, pointing to the need of regulating the use of transgenic substances and of specific labeling in this product category.
机译:目的:这项工作的目的是调查在巴西出售的肠内营养配方食品中是否存在抗农达大豆。方法:基于凝集素基因的扩增和耐草甘膦转基因大豆(35S启动子和叶绿体转运肽基因)的重组脱氧核糖核酸的构建,进行了双链聚合酶链反应,以分析从9种大豆中获得的脱氧核糖核酸。含大豆分离蛋白的配方。结果:尽管食品基质具有高度加工性,但根据凝集素基因序列的扩增判断,从所有测试样品中均获得了可扩增的脱氧核糖核酸模板。但是,与Roundup Ready大豆相比,扩增子仅限于所分析的九种肠内营养配方之一以及大豆参比粉,符合预期。通过实时聚合酶链反应对转基因配方进行的定量分析显示,来自农达就绪大豆的重组脱氧核糖核酸含量约为0.3%(w / w)。结论:结果表明,其中一个配方包含转基因大豆,表明需要调节该产品类别中转基因物质的使用和特定标记。

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