Identification of Panax ginseng, P. notoginseng and P. quinquefolius admixture by multiplex allele-specific polymerase chain reaction

• Published in: Zhongguo zhongyao zazhi Vol. 42; no. 7; p. 1319
• Main Authors: Jiang, Chao, Luo, Yu-Qing, Yuan, Yuan, Huang, Lu-Qi, Jin, Yan, Zhao, Yu-Yang
• Format: Journal Article
• Language: Chinese
• Published: China 01.04.2017
• Subjects: Alleles; DNA Primers; Panax - classification; Panax - genetics; Polymerase Chain Reaction; Species Specificity; Panax notoginseng; admixture; multiplex allele-specific polymerase chain reaction; molecular identification; Panax ginseng; Panax quinquefolius
• ISSN: 1001-5302
• DOI: 10.19540/j.cnki.cjcmm.20170222.001

To achieve a molecular method to identify Panax ginseng, P. notoginseng,P. quinquefolius and their admixture. The ITS,18S and matK sequences of Panax genus were analyzed to develop species-specific SNP marker. Three pairs of species-specific primers were designed to establish a multiplex allele-specific polymerase chain reaction (MAS-PCR) and the samples from different region were tested. The results showed that when the annealing temperature was 60 ℃ and the cycle number was 35, approximately 250, 500,1 000 bp specific band were obtained from P. ginseng, P. notoginseng and P. quinquefolius obtain, respectively. This method could also be used to authentificate admixture samples and could detect 0.5% percent of P. notoginseng or P. quinquefolius adulterated in P. ginseng, or 0.5% percent of P. ginseng or P. quinquefolius adulterated in P. notoginseng. The detect limit of P. ginseng in P. quinquefolius was 0.5% and P. notoginseng in P. quinquefolius was 1%. This results showed that the present method could be used as a promise method to identify Panax ginseng, P. notoginseng, P. quinquefolius and their admixture.