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Easy DNA extraction for rapid detection of Panax ginseng C. A. Meyer in commercial ginseng products.

Serrone PD, Attorri L, Palazzino G

Consiglio per Ricerca e sperimentazione in Agricoltura C.R.A., Rome, Italy. paola.delserrone@isz.it

An investigation was carried out in order to obtain an easy and rapid detection of Panax ginseng in commercial herbal products by using molecular techniques (polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP)). Two protocols and one commercial kit for DNA extraction were used. Four forms of commercial products were considered, i.e., dried body roots, dried root tails, dried root prongs and dried extracts. The RFLP of DNA amplified products by 18df/28ccr primers, obtained using Inf I, Sau 3A1 and Taq I endonucleases, allowed the identification of P. ginseng and its differentiation from P. quinquefolium. The presence of adulterants, as Mirabilis jalapa L. and Phytolacca acinosa Roxb. was excluded in the examined commercial samples. P. ginseng was detected in 63% of the considered samples according to the declaration of the labels, whereas negative results were obtained with the dried extract form. Therefore, the Invitrogen DNA extraction kit let the easy extraction of useful amounts of DNA and a standardisation of routine work, in comparison with the other molecular protocols so far used.

Published 13 September 2007 in Nat Prod Res, 21(12): 1099-103.
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