Duan Zhonggang, Song Wei, Chen Kuan, Qiao Xue, Ye Min
School of Life Science, Huizhou University.
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University.
Biol Pharm Bull. 2017 Oct 1;40(10):1638-1645. doi: 10.1248/bpb.b17-00020. Epub 2017 Jul 26.
Curcumae Longae Rhizoma (Curcuma longa L.) is an important traditional Chinese medicine with multiple beneficial effects. To elucidate the genetic and chemical differences among Curcumae Longae Rhizoma samples, three DNA barcoding markers (rbcL, matK, and ITS-LSU D1/D3) and HPLC fingerprinting were employed in this study. The discriminatory power of rbcL and matK was low, as they only detected one sequence type that showed 100% similarity with more than 20 congeneric species in the Barcode of Life Data Systems (BOLD) database. In contrast, ITS-LSU D1/D3 showed sufficient discriminatory power to precisely identify all of the market samples as C. longa L. in a BLAST search as well as differentiate each sample based on 2-10 ITS-LSU D1/D3 haplotypes with intragenomic variability (mean p-distance: 0.7%, range: 0-2.6%; mean number of differences: 9.6 sites, range: 0-38 sites). HPLC fingerprinting of 13 commercial samples showed a similarity that ranged from 0.769 to 0.996, indicating that the sample quality varied. A cluster analysis based on 5 common peak areas from the HPLC chromatogram resulted in two groups. Group I included 9 samples with a relatively high chemical content, and group II contained 4 samples with a low chemical content. A Mantel test revealed a low correlation (r=0.1721, p=0.047) between genetic and chemical differences. Our findings suggest that the integrated approach of ITS-LSU D1/D3 DNA barcoding and HPLC fingerprinting provides a comprehensive, precise, and convenient method to clarify the genetic and chemical differences in Curcumae Longae Rhizoma.
姜黄是一种具有多种有益功效的重要传统中药。为阐明姜黄样品之间的遗传和化学差异,本研究采用了三种DNA条形码标记(rbcL、matK和ITS-LSU D1/D3)以及高效液相色谱指纹图谱法。rbcL和matK的鉴别能力较低,因为它们仅检测到一种序列类型,该序列类型在生命条形码数据系统(BOLD)数据库中与20多个同属物种显示出100%的相似性。相比之下,ITS-LSU D1/D3显示出足够的鉴别能力,能够在BLAST搜索中准确地将所有市场样品鉴定为姜黄,并基于2-10个具有基因组内变异性的ITS-LSU D1/D3单倍型区分每个样品(平均p距离:0.7%,范围:0-2.6%;平均差异数:9.6个位点,范围:0-38个位点)。13个商业样品的高效液相色谱指纹图谱显示相似度在0.769至0.996之间,表明样品质量存在差异。基于高效液相色谱图中5个共同峰面积的聚类分析产生了两组。第一组包括9个化学含量相对较高的样品,第二组包含4个化学含量较低的样品。Mantel检验显示遗传差异和化学差异之间的相关性较低(r=0.1721,p=0.047)。我们的研究结果表明,ITS-LSU D1/D3 DNA条形码和高效液相色谱指纹图谱的综合方法为阐明姜黄的遗传和化学差异提供了一种全面、精确且便捷的方法。