4.7 Article

The genetic authentication of Panax ginseng and Panax quinquefolius based on using single nucleotide polymorphism (SNP) conducted in a nucleic acid test chip

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 414, 期 13, 页码 3987-3998

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-022-04044-0

关键词

Single nucleotide polymorphism; DNA hybridization; Ginseng authentication; Microfluidic chip; Centrifugal force; Fluorescence detection

资金

  1. NSERC
  2. Macan Biotechnologies Ltd. of Macau

向作者/读者索取更多资源

Panax ginseng and Panax quinquefolius, commonly known as Chinese ginseng and American ginseng, have similar physical appearances, making it difficult to differentiate them. A molecular technique based on nucleic acid testing has been developed to accurately distinguish between the two ginseng species.
Panax ginseng and Panax quinquefolius, which are commonly called Chinese ginseng and American ginseng respectively, have different medicinal properties and market values; however, these samples can be difficult to differentiate from one another based on physical appearances of the samples especially when they are in powdery or granular forms. A molecular technique is thus needed to overcome this difficulty; this technique is based on the nucleic acid test (NAT) conducted on the microfluidic chip surface. Three single nucleotide polymorphism (SNP) sites (i.e. N1, N2, N3) on the Panax genome that differ between P. ginseng (G) and P. quinquefolius (Q) have been selected to design probes for the NAT. Primers were designed to amplify the antisense strands by asymmetric PCR. We have developed three different NAT methodologies involving surface immobilization and subsequent (stop flow or dynamic) hybridization of probes (i.e. N1G, N1Q, N2G, N2Q, N3Q) to the antisense strands. These NAT methods consist of two steps, namely immobilization and hybridization, and each method is distinguished by what is immobilized on the microfluidic chip surface in the first step (i.e. probe, target or capture strand). These three NATs developed are called probe-target method 1, target-probe method 2 and three-strand complex method 3. Out of the three methods, it was found that the capture strand-target-probe method 3 provided the best differentiation of the ginseng species, in which a 3' NH2 capture strand is first immobilized and the antisense PCR strand is then bound, while N2G and N3Q probes are used for detection of P. ginseng (G) and P. quinquefolius (Q) respectively.

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