首页> 外文期刊>Frontiers in Plant Science >Candidate DNA Barcode Tags Combined With High Resolution Melting (Bar-HRM) Curve Analysis for Authentication of Senna alexandrina Mill. With Validation in Crude Drugs
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Candidate DNA Barcode Tags Combined With High Resolution Melting (Bar-HRM) Curve Analysis for Authentication of Senna alexandrina Mill. With Validation in Crude Drugs

机译:候选DNA条形码标签结合高分辨率熔解(Bar-HRM)曲线分析对 Senna alexandrina Mill进行身份验证。在粗药物验证中

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Senna alexandrina (Fabaceae) is a globally recognized medicinal plant for its laxative properties as well as the only source of sennosides, and is highly exported bulk herb from India. Its major procurement is exclusively from limited cultivation, which leads to risks of deliberate or unintended adulteration. The market raw materials are in powdered or finished product form, which lead to difficulties in authentication. Here, DNA barcode tags based on chloroplast genes ( rbcL and matK ) and intergenic spacers ( psbA-trnH and ITS ) were developed for S. alexandrina along with the allied species. The ability and performance of the ITS1 region to discriminate among the Senna species resulted in the present proposal of the ITS1 tags as successful barcode. Further, these tags were coupled with high-resolution melting (HRM) curve analysis in a real-time PCR genotyping method to derive Bar-HRM (Barcoding-HRM) assays. Suitable HRM primer sets were designed through SNP detection and mutation scanning in genomic signatures of Senna species. The melting profiles of S. alexandrina and S . italica subsp. micrantha were almost identical and the remaining five species were clearly separated so that they can be differentiated by HRM method. The sensitivity of the method was utilized to authenticate market samples [Herbal Sample Assays (HSAs)]. HSA01 ( S. alexandrina crude drug sample from Bangalore) and HSA06 ( S. alexandrina crude drug sample from Tuticorin, Tamil Nadu, India) were found to be highly contaminated with S . italica subsp. micrantha . Species admixture samples mixed in varying percentage was identified sensitively with detection of contamination as low as 1%. The melting profiles of PCR amplicons are clearly distinct, which enables the authentic differentiation of species by the HRM method. This study reveals that DNA barcoding coupled with HRM is an efficient molecular tool to authenticate Senna herbal products in the market for quality control in the drug supply chain. CIMAP Communication Number: CIMAP/PUB/2017/31.
机译:番泻叶番泻叶(豆科)是全球公认的药用植物,具有通便通便的特性,也是苦参皂苷的唯一来源,是印度大量出口的散装草药。它的主要采购完全来自有限的种植,这会导致故意或意外掺假的风险。市场上的原料是粉末状或成品形式,这会导致认证困难。在这里,基于叶绿体基因(rbcL和matK)和基因间隔子(psbA-trnH和ITS)的DNA条形码标签是与亚历山大藻及其盟友一起开发的。 ITS1区域区分番泻叶物种的能力和性能导致了ITS1标签作为成功条形码的当前提议。此外,这些标签与实时PCR基因分型方法中的高分辨率熔解(HRM)曲线分析相结合,以得出Bar-HRM(Barcoding-HRM)分析。通过SNP检测和Senna物种基因组特征的突变扫描,设计了合适的HRM引物组。 S. alexandrina和S.的熔化曲线。 italica subsp。 micrantha几乎是相同的,其余五个物种被清楚地分开,以便可以通过HRM方法区分它们。该方法的灵敏度可用于鉴定市场样本[草药样本分析(HSA)]。发现HSA01(得自班加罗尔的亚历山大克氏菌原始药物样品)和HSA06(得自印度的泰米尔纳德邦Tuticorin的S.alexandrina药物样品)被S.高度污染。 italica subsp。 micrantha。通过检测低至1%的污染物,可以灵敏地鉴定出以不同百分比混合的物种混合物样品。 PCR扩增子的熔解曲线明显不同,这可以通过HRM方法实现物种的可靠区分。这项研究表明,DNA条形码与HRM结合是一种有效的分子工具,可在市场上鉴定番泻叶草药产品,以进行药物供应链中的质量控制。 CIMAP通信号:CIMAP / PUB / 2017/31。

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