Secondary Metabolites of Medicinal Plants. Bharat Singh

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Secondary Metabolites of Medicinal Plants - Bharat Singh

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alt="Illustration of the tautomeric structures of Isoazadironolide and Nimbinone."/> Illustration of the tautomeric structures of Nimbiol, Nimbione, and Nimbionol. Illustration of the tautomeric structures of Nimbionone and Nimbisonol. Illustration of the tautomeric structures of Nimbocinone and Nimbocetin. Illustration of the tautomeric structures of Nimbochalcin, Nimbocidin1, and Nimbocidin2. Illustration of the tautomeric structure of salannolide. Illustration of the tautomeric structure of Nimbinolide. Illustration of the tautomeric structures of Nimbolide B and Nimbic acid B. Illustration of the tautomeric structures of Azadirachtin H and Isonimbolide. Illustration of the tautomeric structures of Azadirachtin I and Azadirachtin K. Illustration of the tautomeric structures of Salimuzzalin and Meliacinin. Illustration of the tautomeric structures of γ-Elemene and Phytol. Illustration of the tautomeric structures of Methyl petroselinate and Butyl palmitate. Illustration of the tautomeric structures of Octacosane and α-farnesene. Illustration of the tautomeric structures of Hexahydrofarnesyl acetone and Methyl 14-methylpentadecanoate. Illustration of the tautomeric structures of Lineoleoyl chloride and Nonacosane. Illustration of the tautomeric structures of Eicosane and Hentriacontane.

      To achieve maximum production of azadirachtin, organized and unorganized calli derived from various explants (zygotic embryo, leaf, and ovary) were investigated. The zygotic embryo-derived calli were more suitable for higher accumulation of azadirachtin than leaf and ovary-derived callus cultures. Similarly, higher biosynthesis of azadirachtin was observed in organized calli, while unorganized callus cultures contain the least amount of azadirachtin (Singh and Chaturvedi 2013). A. indica has its origin linked to Indian history and is considered as a symbol of health. Several phytochemicals have been isolated from this plant species (Biswas et al. 2002). The isolated phytochemicals (azadirachtin A, nimbin, and salannin) demonstrated several biological activities (Subapriya and Nagini 2005). The production of azadirachtin was optimized by manipulating in vitro cell cultures (Veerasham et al. 1998; Wewetzer 1998; Jarvis and Morgan 2000) and cell suspension cultures (Kuruvilla et al. 1999; Balaji et al. 2003; Raval et al. 2003). Nimbin accumulation was observed in both callus cultures (Sanyal et al. 1981) and in in vitro regenerated shoots and roots of neem (Srividya and Devi 1998), but salannin accumulation was not reported in tissue cultures (Babu and Nair 2004). The callus regenerated by intermodal segments contains azadirachtin A, nimbin, and salannin (Babu et al. 2006).

      Gradual enhancement of biomass and azadirachtin production was assessed in neem cell suspension cultures. By increasing the nitrate levels in cell suspension cultures, the maximum enhancement of azadirachtin accumulation was reported. It was proposed that the higher nitrate concentration increased the cell permeability, which also enhances the leaching of azadirachtin into culture medium (Prakash and Srivastava 2005, 2006). The cell cultures also promoted higher accumulation of azadirachtin in wild tree species of A. indica in Sri Lanka (Allan et al. 1994; Eeswara et al. 1997). For further enhancement of azadirachtin accumulation in cell cultures, the culture medium was supplemented with picloram and BAP with different concentrations (Kaii-a-Kamb et al. 1992; Fulzele and Satdive 2001; Satdive et al. 2011).

      Due to biopesticide property of azadirachtin, it has attracted the attention of researchers to enhance the production. The calli were regenerated on Woody Plant Medium (liquid medium) supplemented with glucose, casein hydrolysate, and methyl jasmonate. The maximum accumulation was achieved in methyl jasmonate elicited cells. Methyl jasmonate as signal transducer enhanced the secondary metabolism in plant cells that might have induced the production of azadirachtin (Rodrigues et al. 2014). Normally azadirachtin B was not detectable by normal characterization methods in somatic embryos, but the extract of somatic embryos affected the larval development of locusts (Schaaf et al. 2000; Prakash et al. 2002; Festucci-Buselli et al. 2008; Nakabayashi et al. 2010).

      To find the effect of azadirachtin A on callus induction, the seedlings used as explant selected from those seeds, which were having high azadirachtin concentration. The seedlings were inoculated on MS culture medium supplemented with NAA. The observed results revealed that the callus induction was rapid and more proliferative in this explant. In addition, the leaf explant was also used and exposed to clod treatment. The biochemical studies revealed that azadirachtin concentration was higher in those calli that were induced from the cotyledons of higher azadirachtin containing seeds (Kota et al. 2006; Rafiq and Dahot 2010).

      Azadirachtin, an important biopesticide, is one of the active compounds obtained from seeds of neem. To reduce the effectivity of barriers of variation in its source, availability, genetic diversity, and purity maintenance, the tissue culture studies with elicitation are considered as an important technique (Savitha et al. 2006). With the incorporation of fungal elicitors in cell cultures, fourfold production of azadirachtin was enhanced. Similarly, cyanobacterial elicitors were also used for the enhancement of azadirachtin production (Poornasri Devi et al. 2008).

      Azadirachtin is considered as potent biopesticide. Effects of Nitsch, Gamborg, and MS medium were investigated. Nitsch medium was found more suitable than other types of media in increasing the production

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