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Genetic and chemical diversity of Eleutherococcus senticosus and molecular identification of Siberian ginseng by PCR-RFLP analysis based on chloroplast trnK intron sequence
Authors:Shu Zhu  Yanjing Bai  Mayuko Oya  Ken Tanaka  Katsuko Komatsu  Takuro Maruyama  Yukihiro Goda  Takeshi Kawasaki  Masao Fujita  Toshiro Shibata
Affiliation:1. Division of Pharmacognosy, Department of Medicinal Resources, Institute of Natural Medicine, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan;2. Division of Pharmacognosy, Phytochemistry and Narcotics, National Institute of Health Sciences, 1-18-1 Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan;3. Uchida Wakan-yaku Co., Ltd., 4-4-10 Higashinippori, Arakawa-ku, Tokyo 116-8571, Japan;4. Hokkoido Division, Research Center for Medicinal Plant Resources, National Institute of Biomedical Innovation, 108-4 Ohashi, Nayoro, Hokkaido 096-0065, Japan
Abstract:Siberian ginseng (SG), the rhizome and root of Eleutherococcus senticosus, has been used as a tonic and anti-fatigue agent in northeastern Asia from ancient time. In recent years, SG has been becoming fairly popular as dietary supplements and health foods worldwide. In order to establish a convenient and sensitive method for authentication, chloroplast trnK intron sequences of 6 Eleutherococcus species were determined and compared. Genetic polymorphism, representing by 14 types of trnK intron sequence, in E. senticosus was observed. However, characteristic nucleotide markers stable within this species enabled clear discrimination of it from other congeners. A PCR-RFLP method was further developed, which was demonstrated to be efficient for authentication of crude drugs as well as health foods. Quantitative evaluation of three main bioactive constituents indicated chemical diversity in E. senticosus collected from northeast China and the results suggested good producing areas of SG. The chemical data clearly revealed that E. sessliflorus was unsuitable to be used as SG.
Keywords:Eleutherococcus senticosus   Genetic polymorphism   Molecular identification   trnK intron sequence   PCR-RFLP   Eleutheroside B
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