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[芍药根的核糖体DNA内转录间隔区(rDNA-ITS)序列分析及相似度研究]

[Analysis of rDNA-ITS sequences and similarity of radix paeoniae].

作者信息

Liu Juan, Liu Chun-Sheng, Wei Sheng-Li, Zhang Ji, Zheng Jian

机构信息

School of Chinese Materia Medica, Beijing University of Traditional Chinese Medicine, Beijing 100102, China.

出版信息

Zhong Yao Cai. 2011 Oct;34(10):1517-21.

Abstract

OBJECTIVE

To establish molecular authentication standards of Radix Paeoniae.

METHODS

PCR method was used to determine rDNA-ITS sequences of sample S1 and sample S2 including ITS1, 5.8S, and ITS2. The sequences were analyzed by BLAST and DNAMAN software. rDNA-ITS sequences of Paeonia lactiflora Pall., Paeonia veitchii Lynch. and their counterfeit were analyzed by DNAMAN software.

RESULTS

Established three molecular authentication standards on Radix Paeoniae: (1) The genera of samples was determined by the results of BLAST; (2) The species of samples were determined by the similarities; (3) The specific base positions confirmed the species of samples. Based on the sequence alignment and base differences, sample S1 was identified as Paeonia lactiflora Pall., and sample S2 was identified as Paeonia veitchii Lynch.

CONCLUSION

This paper can give an effective way of Radix Paeoniae identification. What's more, it gives a good example for other Chinese Medicinal Materia authentication.

摘要

目的

建立芍药根的分子鉴定标准。

方法

采用PCR方法测定样品S1和样品S2的rDNA-ITS序列,包括ITS1、5.8S和ITS2。利用BLAST和DNAMAN软件对序列进行分析。使用DNAMAN软件分析芍药、川赤芍及其伪品的rDNA-ITS序列。

结果

建立了芍药根的三个分子鉴定标准:(1)通过BLAST结果确定样品的属;(2)通过相似度确定样品的种;(3)特定碱基位置确认样品的种。基于序列比对和碱基差异,样品S1被鉴定为芍药,样品S2被鉴定为川赤芍。

结论

本文可为芍药根的鉴定提供有效方法。此外,它为其他中药材鉴定提供了一个很好的范例。

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