Bharat Singh

Secondary Metabolites of Medicinal Plants


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in C. roseus cell platforms. Usually, enzymes of the biosynthetic pathway are selected as targets for gene cloning and then manipulated by genetic engineering, e.g. to increase metabolic flow rate toward the compound of interest and hence enhance its levels. This approach has a limited value since a more predictable control of metabolic flux could be achieved using transcription factors because they can regulate one or more catalytic steps from terpenoid indole alkaloid biosynthesis (Capell and Christou 2004; Giri and Narasu 2000; Goyal et al. 2008). In addition, the complex interactions among biosynthetic pathways and sophisticated regulatory mechanisms further complicate engineering efforts. Therefore, among the strategies used to enhance terpenoid indole alkaloid biosynthesis in C. roseus in vitro cultures, the overexpression of transcription factors and genes of their biosynthetic pathways could be highlighted as well as the overexpression of genes from the terpenoid indole alkaloid biosynthesis in other organisms (Wilson and Roberts 2014).

      The accumulation of vindoline in C. roseus intact plant was 0.2%, a level much higher than that of catharanthine, while the cost of vindoline is less expensive compared to catharanthine and vinblastine. The observed results showed that the MS medium (Murashige and Skoog 1962) was the most favorable for optimization of catharanthine production in different cell lines of C. roseus. Addition of various biotic and abiotic precursors to the medium as “inducers” was found to induce the production of Vinca alkaloids. When abscisic acid was used as an elicitor in cell cultures, the accumulation of catharanthine was raised maximum on the seventh day of cultivation. Circular dichroism confirmed that α-coupling exists between the two monomeric units of both vinblastine and vincristine produced enzymatically (Whitmer et al. 2000). This is an efficient and novel method to produce vinblastine and is likely to be used for the commercialization of vinblastine. The production of anhydrovinblastine was enhanced by a two-enzyme system (horse radish peroxidase and glucose oxidase) for catalyzation of the anhydrovinblastine to catharanthine and vindoline (Bede and DiCosmo 1992; Kumar et al. 2013).

      MS medium supplemented with kinetin and 6-benzylaminopurine (BAP) each with 2,4-D and indole-3-acetic acid (IAA) combinations showed good callus production. Similarly MS + kinetin and BAP 2 mg/l each and MS + 2,4-D and IAA combinations showed green and resin-secreting callus. When the leaf explants were cultured in MS + BAP and 1-naphthaleneacetic acid (NAA), they showed large number of root formation. When combination of MS + kinetin and 2,4-D and MS + BAP and IAA were used, a quick callus induction was seen (Negi 2011; Koul et al. 2013). The production of vinblastine via chemical coupling was enhanced in the presence of ferric chloride, oxalate, maleate, stemmadenine, and sodium borohydride (El-Sayed et al. 2004). Effects of various parameters like stress, addition of bioregulators, elicitors, and synthetic precursors on indole alkaloids production were also studied (Zhao et al. 2001a,b). Metabolic rate limitations through precursor feeding and the effects of elicitor dosage on biosynthesis of indole alkaloids in hairy root cultures of C. roseus have also been studied (Morgan and Shanks 2000; Rijhwani and Shanks 1998; Almagro et al. 2014).

      Alkaloids were produced from callus, roots, and petiole of C. roseus in the presence of kinetin and NAA. MS with NAA + kinetin had the highest vindoline, catharanthine, and vincristine. But the level of these alkaloids and ajmalicine were very low compared to that in the petiole of intact plant, and the level of serpentine was similar. The largest amount of alkaloids was produced in new roots and callus. The indole alkaloid levels of new roots in new media were higher than in petioles of intact plants (El-Sayed and Verpoorte 2007; Courdavault et al. 2014). The most interesting result was the presentation of two important anticancer dimeric alkaloids, 20-fold for vinblastine and sixfold for vincristine, compared with that in the petioles of intact plants (Ataei-Azimi et al. 2008).

      Vinblastine and vincristine are excellent anticancer drugs, but their current production is not abundant and expensive. In order to make these drugs readily available to the patients at affordable prices, the endophytic fungi from C. roseus plant was isolated, thus discovering a fungus AA-CRL-6, which produces vinblastine and vincristine in appreciable amounts (Kumar et al. 2013).

      Conditions for co-culturing the cell suspensions of C. roseus and Vinca major in shake flask and bioreactor are described here for the possible complementation of the terpenoid indole alkaloid pathway. Catharanthus cells could be reared on an MS medium containing NAA and kinetin. A 20- and 40-fold increment in the biomass of these co-cultures was achieved within 30 days in a stirred tank bioreactor. Out of these two alkaloids, compound RF1 was found to possess strong antioxidant potential (Verma et al. 2012). The 3′,4′-di-O-methylquercetin-7-O-[(4′′→13′′′)-2′′′,6′′′,10′′′,14′′′-tetramethylhexadec-13′′′-ol-14′′′-enyl]-β-D-glucopyranoside, 4′-O-methylkaempferol-3-O-[(4′→13′′′)-2′′′,6′′′,10′′′,14′′′-tetramethylhexadecan-13′′′-olyl]-β-D-glucopyranoside, 3′,4′-di-O-methylbutin-7-O-[(6′′→1′′′)-3′′′,11′′′-dimethyl-7′′′-methylenedodeca-3′′′, 10′′′-dienyl]-β-D-glucopyranoside, and 4′-O-methylbutin-7-O-[(6′′→1′′′)-3′′′,11′′′-dimethyl-7′′′-hydroxymethylenedodecanyl]-β-D-glucopyranoside were isolated from the methanol extract of hairy roots of C. roseus (Canel et al. 1998; Bhadra et al. 1993; Batra et al. 2004; Chung et al. 2007, 2009; Hanafy et al. 2016).

      1 Almagro,