基于聚合酶链反应的方法对肠内营养配方中的转基因大豆进行定性和定量评价

N. Barros, E. Oliveira, O. F. Silva, J. T. Silva, V. Paschoalin
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摘要

目的:调查在巴西销售的肠内营养配方中抗农达大豆的出现情况。方法:采用双链聚合酶链反应(pcr),扩增凝集素基因,构建转基因耐草甘膦大豆(35S启动子和叶绿体转运肽基因)重组脱氧核糖核酸,对9种大豆分离蛋白配方中获得的脱氧核糖核酸进行分析。结果:尽管食品基质具有高度加工的性质,但通过凝集素基因序列的扩增判断,从所有测试样品中获得了可扩增的脱氧核糖核酸模板。然而,与抗农达大豆相关的扩增子仅限于所分析的九种肠内营养配方中的一种以及大豆参考粉,正如预期的那样。通过实时聚合酶链反应(real-time Polymerase Chain Reaction)对转基因配方进行定量分析,结果显示转基因大豆中重组脱氧核糖核酸的含量约为0.3% (w/w)。结论:其中一种配方奶含有转基因大豆,需要对转基因物质的使用进行规范,并对该类产品进行专项标识。
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Qualitative and quantitative assessment of genetically modified soy in enteral nutrition formulas by polymerase chain reaction based methods
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.
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