“…Two molecules of farnesyl diphosphate along with squalene synthase (SS) produce squalene, to which an epoxide group of squalene epoxidase (SE) subsequently gives rise to 2,3-oxidosqualene. Ginsenosides are synthesized from the 2,3-oxidosqualene (a common precursor of sterols), which undergoes additional cyclization, hydroxylation, and glycosylation by dammarenediol synthase (DDS), cytochrome P450, and glycosyltransferase (GT) enzymes, respectively (Han et al 2006;Devi et al 2011;Khorolragchaa et al 2014). Three different groups of ginsenosides have been isolated and identified based on their aglycones: protopanaxadiol-type (PPD) saponins such as ginsenosides Rb1, Rb2, Rc, and Rd; protopanaxatriol-type (PPT) saponins such as ginsenosides Re, Rg1, Rg2, and Rf; and the oleanane group with a pentacyclic structure, and only one ginsenoside, Ro, was identified.…”