首页> 外文期刊>Food science and technology research >Development of an Ultra-sensitive Detection Method for Genetically Modified Soybeans in Natto, a Traditional Japanese Fermented Food
【24h】

Development of an Ultra-sensitive Detection Method for Genetically Modified Soybeans in Natto, a Traditional Japanese Fermented Food

机译:开发日本传统发酵食品纳豆中的转基因大豆超灵敏检测方法

获取原文
获取原文并翻译 | 示例
           

摘要

When extracting soybean DNA from natto, a traditional Japanese fermented food, Bacillus subtilis var. natto DNA is commonly present despite fastidious washing of samples. We confirmed that DNA extracted from B. subtilis var. natto inhibited PCR amplification of the soybean endogenous lectin gene (Le1) as well as the recombinant nopaline synthase terminator sequence (Nos-ter), which is used to identify genetically modified soybean (GMS) in natto. To mitigate B. subtilis var. natto DNA contamination, we developed a novel method for the specific extraction of Le1 and Nos-ter genes using DNA probes immobilized on streptavidin-coated magnetic beads with hybridization enhancement blockers, which are capable of enhancing the affinity between the target gene DNA and the probe DNA. By using the proposed extraction method, both Le1 and Nos-ter genes could be detected in samples containing B. subtilis var. natto DNA. DNA extraction from commercial nattos and identification of GMS were also successfully accomplished.
机译:从纳豆(日本传统发酵食品枯草芽孢杆菌)中提取大豆DNA时。尽管对样品进行了严格的洗涤,但纳豆DNA通常还是存在的。我们确认从枯草芽孢杆菌变种中提取DNA。纳豆抑制了大豆内源性凝集素基因(Le1)以及重组胭脂碱合酶终止子序列(Nos-ter)的PCR扩增,该序列用于鉴定纳豆中的转基因大豆(GMS)。为了减轻枯草芽孢杆菌变种。纳豆DNA污染,我们开发了一种新方法,该方法使用固定在抗生蛋白链菌素包被的磁珠上的DNA探针与杂交增强阻滞剂固定化,从而特异性地提取Le1和Nos-ter基因,能够增强目标基因DNA与探针之间的亲和力脱氧核糖核酸。通过使用提出的提取方法,可以在含有枯草芽孢杆菌变种的样品中检测到Le1和Nos-ter基因。纳豆DNA。从商业样品中提取DNA并鉴定GMS也已成功完成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号