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Ginsenosides as Quality Indicators in Woods-grown American Ginseng
Kenneth Mudge, Wansang Lim, Joe Lardner and V. Jousselin
Department of Horticulture, Cornell University, Ithaca, NY

 

Introduction

American ginseng (Panex quinquefolium) is a valuable alternative medicinal root crop. The value of this shade loving crop is greatly influenced by how the crop is grown (Table 1). Wild populations are increasingly scarse, and intensively cultivated field-grown ginseng is overproduced and deemed to be of low quality. Forest farming (Woods Cultivation) of this shade loving crop in natural forest woodlots is a low input, comparatively high value alternative to intensive horticultural production and wild collection.

Table 1. Root Value (per dry pound)
Wild $500 - 600
Woods Cultivated $200 - 300

Field Cultivated

$ 20- 30

Quality Evaluation

Ginseng quality and price has traditionally been judged by root shape, texture, age, and rate of growth. Root branching resulting in a man-like form is highly valued. Pharmacologically, the active medicinal principles of the herb are a group of triterpene saponins known as ginsenosides. Ginsenoside Rb1, shown to the right, is the most abundant of the twenty plus known ginsenosides. A correlation between quality judged by traditional criteria, and ginsenoside content is widely assumed but largely unsubstantiated. It has also been reported (Betz, 1984), but not widely confirmed, that wild ginseng is higher in ginsenoside content than cultivated root.

 

Experimental Approach

To test the hypothesis that ginseng from different geographic sources (presumed genotypes) differ in ginsenocide content, ginseng roots from 7 different geographic sources were grown at a single naturally forested provenance garden in Chemung County, NY (Phetteplace, Raw Furs) for several years. In June, 2000, roots were collected for ginsenoside analysis by HPLC (Figure 1).

Figure 1. Ginsenocide Extraction, Purification and Analysis

(adapted from Court et al., 1996)

Air dry root
¯
Extract in 70% MeOH
¯
Centrifuge
¯
Concentrate In vacuo
¯
HPLC (RP C18, Acetonitrile/H2O)
¯
Identification and Measurement

qualitative i.d. by coelution w/known standards
quantifcation by UV light absorption at 203 nm

 

HPLC chromatogram of a typical ginseng root sample

 

 

UV203nm absorbance

Retention time, min.

Results

Figure 2 shows the concentration (% dry wt.) of six common ginsenocides and the total ginsenocide content from roots originating from each of seven geographic sources, all grown for several years at a common location. Statistical analysis of the levels of individual ginsenocides showed significant variation between geographic sources, as shown for the most abundant ginsenocide, Rb1(Figure 3). In addition to variation in ginsenocide content between populations, there was considerable variation between roots within populations, as shown in Figure 4.

 

What have we learned?


Figure 5. Ginseng root-derived callus culture, underway in our laboratory, to develop a somatic embryogenesis-based system for cloning superior genotypes.

 

Literature Cited

Betz,JM, AH Der Morderosian & TM Lee, 1984, Proc. 6th N.American Ginseng Conf. Guelph, Ontario pp 65-83.

Court, WA, JG Hendel and J Elmi, 1996, Journal of Chromatography A, 775:11-17.

 

"Copyright Cornell University, 2001"

 

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