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名贵中药材血竭的DNA条形码鉴定研究 被引量:16
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作者 王俊 刘霞 +5 位作者 孙伟 汪波 李丹平 樊佳佳 张晓存 陈士林 《中国药学杂志》 CAS CSCD 北大核心 2015年第15期1261-1265,共5页
目的筛选适合树脂类药材血竭鉴定的DNA条形码序列,探索血竭药材鉴定的新方法。方法提取41份药材和基原植物样本的基因组DNA,对药材样本基因组DNA的7条候选条形码序列[ITS、ITS2、psb A-trn H、rbc L、mat K、trn L(UAA)内含子、trn L(U... 目的筛选适合树脂类药材血竭鉴定的DNA条形码序列,探索血竭药材鉴定的新方法。方法提取41份药材和基原植物样本的基因组DNA,对药材样本基因组DNA的7条候选条形码序列[ITS、ITS2、psb A-trn H、rbc L、mat K、trn L(UAA)内含子、trn L(UAA)内含子的P6环]进行PCR扩增及测序。采用软件Codon Code Aligner V4.2对测序峰图进行校对拼接,应用MEGA5.0软件计算种内种间遗传距离(Kimura 2-parameter),构建邻接树(Neighbor-joing tree,NJ Tree)。结果血竭药材的trn L(UAA)内含子的P6环序列可以成功扩增并得到高质量序列,而其他6个候选序列[ITS、ITS2、psb A-trn H、rbc L、mat K、trn L(UAA)内含子]均不能成功扩增,难以用于鉴别。血竭的trn L(UAA)内含子的P6环序列长度为45 bp,麒麟竭的种内最大K2P遗传距离远小于麒麟竭与品剑叶龙血树的种间最小K2P遗传距离,NJ树显示血竭与其混伪品各自聚为一支,可明显区分。结论 trn L(UAA)内含子的P6环序列可作为血竭药材的DNA条形码鉴定序列,成为血竭药材真伪的鉴定依据。 展开更多
关键词 血竭 树脂 DNA条形码 trnl(uaa)内含子 p6
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管花肉苁蓉、菊花、人参药材及其加工品的DNA条形码鉴定研究 被引量:2
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作者 宋明 董刚强 +3 位作者 张雅琴 赵海誉 刘霞 孙伟 《中国药学杂志》 CAS CSCD 北大核心 2015年第17期1485-1489,共5页
目的利用DNA条形码技术对管花肉苁蓉、菊花、人参药材及其加工品进行鉴定,为中药以及食品的质量检测提供了新的技术手段。方法该研究以ITS2序列和trn L(UAA)内含子P6环序列作为参考序列,对实验样品进行DNA提取,PCR扩增和双向测序,利用... 目的利用DNA条形码技术对管花肉苁蓉、菊花、人参药材及其加工品进行鉴定,为中药以及食品的质量检测提供了新的技术手段。方法该研究以ITS2序列和trn L(UAA)内含子P6环序列作为参考序列,对实验样品进行DNA提取,PCR扩增和双向测序,利用相似性搜索法和软件MEGA5.0对序列进行比对分析。结果研究表明,ITS2序列能够准确鉴定管花肉苁蓉和人参药材样本,trn L(UAA)P6序列能够在高度降解的DNA样本成功扩增,管花肉苁蓉、菊花和人参加工品的trn L(UAA)P6序列与其药材完全一致,无任何变异位点,但通过相似性搜索法无法将加工品鉴定到种的水平。结论应用ITS2序列可以准确鉴定DNA条形码对管花肉苁蓉和人参药材,trn L(UAA)P6序列在中药以及食品的质量检测中具有很好的应用前景。 展开更多
关键词 DNA条形码 trnl(uaa)p6 ITS2 鉴定
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Identification of processed Chinese medicinal materials using DNA mini-barcoding 被引量:7
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作者 SONG Ming DONG Gang-Qiang +2 位作者 ZHANG Ya-Qin LIU Xia SUN Wei 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2017年第7期481-486,共6页
Most of Chinese medicinal herbs are subjected to traditional processing procedures, including stir-frying, charring, steaming, boiling, and calcining before they are released into dispensaries. The marketing and ident... Most of Chinese medicinal herbs are subjected to traditional processing procedures, including stir-frying, charring, steaming, boiling, and calcining before they are released into dispensaries. The marketing and identification of processed medicinal materials is a growing issue in the marketplace. However, conventional methods of identification have limitations, while DNA mini-barcoding, based on the sequencing of a short-standardized region, has received considerable attention as a new potential means to identify processed medicinal materials. In the present study, six DNA barcode loci including ITS2, psb A-trn H, rbc L, mat K, trnL(UAA) intron and its P6 loop, were employed for the authentication of 45 processed samples belonging to 15 species. We evaluated the amplification efficiency of each locus. We also examined the identification accuracy of the potential mini-barcode locus, of trnL(UAA) intron P6 loop. Our results showed that the five primary barcode loci were successfully amplified in only 8.89%——20% of the processed samples, while the amplification rates of the trnL(UAA) intron P6 loop were higher, at 75.56% successful amplification. We compared the mini-barcode sequences with Genbank using the Blast program. The analysis showed that 45.23% samples could be identified to genus level, while only one sample could be identified to the species level. We conclude that trnL(UAA) p6 loop is a candidate mini-barcode that has shown its potential and may become a universal mini-barcode as complementary barcode for authenticity testing and will play an important role in medicinal materials control. 展开更多
关键词 DNA barcoding trnl(uaa)intron p6 loop IDENTIFICATION PROCESSED MEDICINAL MATERIALS Mini-barcode
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