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首页> 外文期刊>日本農芸化学会誌 >Identification of domestic glutinous rice cultivars by the PCR method using grains of 18 typical glutinous rice cultivars as sample and development of technology for detection of different kind grain incorporation in glutinous rice processed foodstuf
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Identification of domestic glutinous rice cultivars by the PCR method using grains of 18 typical glutinous rice cultivars as sample and development of technology for detection of different kind grain incorporation in glutinous rice processed foodstuf

机译:以18种典型糯米品种为样本的PCR方法鉴定国产糯米品种及糯米加工食品中不同类型谷物掺入检测技术的发展。

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摘要

A part of rice for staple food and for crushing rice has been provided as raw materials of processed glutinous rice products. For this background, almost manufacturer can not select raw material rice. Therefore, the technology to warrant quality of raw material rice is indispensable. By PCR using newly developed STS primers, blended corn and barley to glutinous rice products were detected. A part of primers were designed based on reported DNA sequences of Zein and Hordein. And promising primers derived of GBSS were used to amplify the discriminative DNA bands. GBSS genes were extracted from agarose gels of electrophoreses after PCR and cloned into a PCR-XL-TOPO vector followed by sequencing. Therefore, there was a slight difference among corn, barley and rice in DNA sequences of GBSS genes. A part of these different base regions were used to design the primers. These STS primers were showed to be useful to differentiate corn, barley and glutinous rice. DNA extraction from rice craker has some difficulties, however, it became possible to extract and purify by improving 'enzyme method', which we reported previously and extracted DNA could be amplified by PCR. And cultivar identification by the PCR method was investigated using 18 typical domestic glutinous rice cultivars.
机译:已经提供了一部分大米用于主食和碾碎大米,作为加工糯米产品的原料。对于这种背景,几乎制造商无法选择原料大米。因此,保证大米原料质量的技术是必不可少的。通过使用新开发的STS引物进行PCR,检测到玉米和大麦混合成糯米产品。基于玉米醇溶蛋白和大麦醇溶蛋白的报道的DNA序列设计了一部分引物。 GBSS衍生的有前途的引物被用于扩增区分性DNA条带。 PCR后,从电泳琼脂糖凝胶中提取GBSS基因,并将其克隆到PCR-XL-TOPO载体中,然后进行测序。因此,GBSS基因的DNA序列在玉米,大麦和水稻之间略有差异。这些不同碱基区域的一部分用于设计引物。这些STS引物被证明可用于区分玉米,大麦和糯米。从大米中提取DNA有一定困难,但是,通过改进“酶法”就可以提取和纯化,我们先前报道过,提取的DNA可以通过PCR进行扩增。并利用18个典型的国内糯稻品种,通过PCR方法进行了品种鉴定。

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