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应用DNA条形码技术对市场苦木药材的检测研究
引用本文:陈影,张景景,汤欢,王俊,赵李龙,孙伟.应用DNA条形码技术对市场苦木药材的检测研究[J].世界科学技术-中医药现代化,2016(1):46-52.
作者姓名:陈影  张景景  汤欢  王俊  赵李龙  孙伟
作者单位:中国中医科学院 中药研究所 中药鉴定与安全性检测评估北京市重点实验室 北京 100700,南阳理工学院张仲景国医国药学院 南阳 473000,四川农业大学林学院 成都 611130,武汉理工大学化学化工与生命科学学院 武汉 430070,南阳理工学院张仲景国医国药学院 南阳 473000,中国中医科学院 中药研究所 中药鉴定与安全性检测评估北京市重点实验室 北京 100700
基金项目:科学技术部国家重大新药创制项目(2013ZX09301307):基于中医临床转化的中药创新品种研发,负责人:陈士林。
摘    要:利用DNA条形码技术对市场上中药材苦木进行检测,为其市场监管及用药安全提供保障。方法:对15份苦木药材(每份取样2个)共30个样品进行DNA提取,PCR扩增其ITS2序列并双向测序,应用CodonCode Aligner version 6.0.2软件对测序峰图进行校对拼接,将得到的所有序列与GenBank以及中药材DNA条形码鉴定系统分别进行比对,选择相似度最相近的物种在中国植物志网站上查询。在此基础上扩增其psbA-trnH 序列以验证结果的可靠性。结果:市场购买的苦木样品中正品苦木Picrasma quassioides 占70%、臭椿Ailanthus altissima占6.67%、板蓝Baphicacanthus cusia占13.33%、楝叶吴茱萸Tetradium glabrifolium占3.33%、柘Maclura tricuspidata 占6.67%。结论:市场上苦木药材存在混伪品,DNA条形码技术能有效鉴别药材真伪。

关 键 词:苦木  DNA条形码  ITS2序列  psbA-trnH序列
收稿时间:2015/6/16 0:00:00
修稿时间:2015/12/7 0:00:00

DNA Barcoding for Identification of Picrasma quassioides and Its Adulterants on the Market
Chen Ying,Zhang Jingjing,Tang Huan,Wang Jun,Zhao Lilong and Sun Wei.DNA Barcoding for Identification of Picrasma quassioides and Its Adulterants on the Market[J].World Science and Technology-Modernization of Traditional Chinese Medicine,2016(1):46-52.
Authors:Chen Ying  Zhang Jingjing  Tang Huan  Wang Jun  Zhao Lilong and Sun Wei
Institution:Institute of Chinese Materia Medica,China Academy of Chinese Medical Sciences,Key Laboratory of Beijing for Identification and Safety Evaluation of Chinese Medicine,Beijing 100700,China,Zhang Zhong-jing Traditional Chinese Medicine College,Nanyang Institute of Technology,Nanyang 473000,China,College of Forestry,Sichuan Agricultural University,Chengdu 611130,China,School of Chemical Engineer ing and Life Sciences,Wuhan University of Technology,Wuhan 430070,China
Abstract:DNA barcoding technology was employed for identifying commercial products called Picrasma quassioides on the market.This study provided a guarantee for the market supervision and drug safety.Genomic DNA (2 repeats for each sample) from 15 P.quassioides samples was extracted.The ITS2 sequences were amplified and bidirectionally sequenced.All sequences were assembled and obtained using the CodonCode Aligner version 6.0.2.All sequences were compared with sequences available in the GenBank and TCMBARCODE database.The highest similarity species were selected and searched on the website of Flora Reipublicae Popularis Sinicae.In addition,the psbA-trnH sequences were amplified to verify the reliability of the results.The results showed that P.quassioides (70%),Ailanthus altissima(6.67%),Baphicacanthus cusia(13.33%),Tetradium glabrifolium (3.33%)and Maclura tricuspidata(6.67%)were found in the commercial samples.It was concluded that there were some adulterants of P.quassioides on the market. DNA barcoding technology can effectively monitor the medicines from its adulterants.
Keywords:Picrasma quassioides  DNA barcoding  ITS2 sequence  psbA-trnH sequence
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