“Panax ginseng Meyer, which is commonly known as Korean gi


“Panax ginseng Meyer, which is commonly known as Korean ginseng, is one

of the most important traditional medicines in East Asia. Triterpene glycoside saponin, named ginsenoside, is the main bioactive ingredient in P. ginseng and is known to exhibit various pharmacological and physiological effects including anticancer [1], [2] and [3], antidiabetic [4] and [5], immunomodulatory [1] and [6], neuroprotective [1], radioprotective [7], antiamnestic [1], and antistress properties [8] and [9]. The natural role of saponins in plants has been suggested to play a defensive role against pathogen and pest attacks [10]. The most important physiological role of ginsenosides in the ginseng plant is part of the defense mechanisms from pathogen attacks [11]. Naturally occurring ginsenosides are present to protect the ginseng from microbial and ABT-199 fungal infection; the bitter taste of ginsenosides makes them antifeedants [12], [13], [14], [15] and [16]. Ginsenoside is contained in ginseng root at >4% by dry weight [17]. Ginsenosides are classified into two groups by the skeleton of aglycones, namely dammarane type and oleanane type. Dammarane-type tetracyclic structure is unique in ginseng, although other oleanane-type triterpenes are also observed in other plants. Dammarane-type ginsenosides consist mainly of two types that are classified

according to their aglycone moieties, protopanaxadiol (PPD) and protopanaxatriol (PPT) ginsenoside. Ginsenoside backbones are synthesized via the isoprenoid pathway by cyclization of 2,3-oxidosqualene Rucaparib mediated by dammarenediol Chk inhibitor synthase (DDS) or β-amyrin synthase (β-AS).

Although many reports have been published regarding the pharmacological effects of ginsenosides, little is known about the ginsenoside biosynthesis pathway or its regulation. Complete cDNA clones for several enzymes from ginseng have been reported. The genes encoding squalene synthase (SS), squalene epoxidase (SE), β-AS, lanosterol synthase, cycloartenol synthase (CAS), and DDS have been identified. Metabolic engineering such as overexpression or gene silencing of those genes has altered ginsenoside levels. Upregulation of ginsenoside levels by elicitors is also an attractive strategy to achieve greater ginsenoside quantities [18]. The accumulation of secondary metabolites can be enhanced by exposing plant cell and tissue cultures to biotic and abiotic elicitors [19]. When plants perceive environmental changes, they generate biological responses through specific signal transduction. Methyl jasmonate (MJ) has been reported to play an important role in the production of antioxidant defense genes and secondary metabolites in plants [20], [21] and [22]. It has been reported that MJ stimulates ginsenoside production in cultured ginseng cells, hairy root, and adventitious roots [23], [24], [25] and [26].

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