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A Nucleotide Signature for the Identification of Angelicae Sinensis Radix (Danggui) and Its Products

机译:当归(当归)及其制品的鉴定用核苷酸标记

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摘要

It is very difficult to identify Angelicae sinensis radix (Danggui) when it is processed into Chinese patent medicines. The proposed internal transcribed spacer 2 (ITS2) is not sufficient to resolve heavily processed materials. Therefore, a short barcode for the identification of processed materials is urgently needed. In this study, 265 samples of Angelicae sinensis radix and adulterants were collected. The ITS2 region was sequenced, and based on one single nucleotide polymorphism(SNP) site unique to Angelica sinensis, a nucleotide signature consisting of 37-bp (5′-aatccgcgtc atcttagtga gctcaaggac ccttagg-3′) was developed. It is highly conserved and specific within Angelica sinensis while divergent among other species. Then, we designed primers (DG01F/DG01R) to amplify the nucleotide signature region from processed materials. 15 samples procured online were analysed. By seeking the signature, we found that 7 of them were counterfeits. 28 batches of Chinese patent medicines containing Danggui were amplified. 19 of them were found to contain the signature, and adulterants such as Ligusticum sinense, Notopterygium incisum, Angelica decursiva and Angelica gigas were detected in other batches. Thus, this nucleotide signature, with only 37-bp, will broaden the application of DNA barcoding to identify the components in decoctions, Chinese patent medicines and other products with degraded DNA.
机译:当归加工成中成药时,很难鉴别当归(当归)。提出的内部转录间隔物2(ITS2)不足以分解处理量大的材料。因此,迫切需要用于识别加工材料的短条形码。在这项研究中,收集了265个当归和掺假样品。对ITS2区进行测序,并基于当归独特的一个单核苷酸多态性(SNP)位点,开发了一个由37 bp(5'-aatccgcgtc atcttagtga gctcaaggac ccttagg-3')组成的核苷酸标记。它在当归内是高度保守的和特异性的,而在其他物种中则有所不同。然后,我们设计了引物(DG01F / DG01R),以从加工材料中扩增核苷酸标记区域。分析了15个在线采购的样品。通过查找签名,我们发现其中有7件是假冒产品。扩增了当归含中药的28批次中成药。发现其中有19个带有签名,在其他批次中还检出了掺假品,如西番莲,切叶Not活,当归和当归。因此,这种仅有37 bp的核苷酸特征将扩大DNA条形码的应用范围,以鉴定煎剂,中成药和其他具有降解DNA的产品中的成分。

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