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A simple real-time polymerase chain reaction (PCR)-based assay for authentication of the Chinese Panax ginseng cultivar Damaya from a local ginseng population

机译:一种简单的基于实时聚合酶链反应(PCR)的检测方法,用于对来自当地人参种群的人参进行鉴定

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Panax ginseng is one of the most important medicinal plants in the Orient. Owing to its increasing demand in the world market, cultivated ginseng has become the main source of medicinal material. Among the Chinese ginseng cultivars, Damaya commands higher prices and is grown in significant proportions among the local ginseng population. Due to the lack of rapid and accurate authentication methods, Damaya is distributed among different cultivars in the local ginseng population in China. Here, we identified a unique, Damaya-specific single nucleotide polymorphism (SNP) site present in the second intron of mitochondrial cytochrome c oxidase subunit 2 (cox2). Based on this SNP, a Damaya cultivar-specific primer was designed and an allele-specific polymerase chain reaction (PCR) was optimized for the effective molecular authentication of Damaya. We designed a method by combining a simple DNA isolation method with real-time allele-specific PCR using SYBR Green I fluorescent dye, and proved its efficacy in clearly discriminated Damaya cultivar from other Chinese ginseng cultivars according to the allelic discrimination analysis. Hence, this study provides a simple and rapid assay for the differentiation and conservation of Damaya from the local Chinese ginseng population.
机译:人参是东方最重要的药用植物之一。由于其在世界市场上的需求增加,栽培人参已成为药用材料的主要来源。在中国人参品种中,达摩亚价格较高,并且在当地人参人口中比例很高。由于缺乏快速,准确的认证方法,达玛亚人分布在中国当地人参种群的不同品种中。在这里,我们确定了在线粒体细胞色素C氧化酶亚基2(cox2)的第二个内含子中存在的独特的Damaya特定单核苷酸多态性(SNP)位点。基于该SNP,设计了Damaya品种特异性引物,并优化了等位基因特异性聚合酶链反应(PCR),以实现Damaya的有效分子鉴定。我们设计了一种方法,将简单的DNA分离方法与使用SYBR Green I荧光染料的实时等位基因特异PCR结合起来,并通过等位基因歧视分析证明了其在将达摩亚品种与其他人参品种清楚地区分的功效。因此,本研究为从当地人参种群中分化和保护达玛雅提供了一种简单而快速的方法。

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