Bioengineering of Tacca integrifolia for production of secondary metabolites with antiproliferative properties / Pathimah @ Fatimah Abdol Latif

Tacca integrifolia or locally known as janggut Adam is a wild plant species which often used to treat gastric ulcer, hypertension, antiproliferative, haemorrhoids, heart failure and kidney disease. Since its geographical distribution is limited, with its poor germination and short-term seed viabilit...

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Bibliographic Details
Main Author: Abdol Latif, Pathimah @ Fatimah
Format: Thesis
Language:English
Published: 2022
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/60988/1/60988.pdf
https://ir.uitm.edu.my/id/eprint/60988/
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Summary:Tacca integrifolia or locally known as janggut Adam is a wild plant species which often used to treat gastric ulcer, hypertension, antiproliferative, haemorrhoids, heart failure and kidney disease. Since its geographical distribution is limited, with its poor germination and short-term seed viability it has raised the issues of short supply and high demand of this plant. Therefore, this study was aimed to develop an in vitro propagation system for T. integrifolia from in vitro seedlings to produce secondary metabolites with anti-proliferative properties. T. integrifolia was previously identified as a potent antiproliferative resource, but scientific information of the metabolomic and pathway study on in vitro plant culture of T. integrifolia is still inadequate and limited to wild plant. Murashige and Skoog (MS) basal medium were used for the growth of seedlings, whilst shoots from the in vitro germinated seedlings were excised and cultured on MS medium containing different PGRs. The optimum numbers of roots, shoots and callus were observed, measured, and analysed statistically after 12 weeks. The metabolites produced from an optimum in vitro culture treatments and wild plant group were profiled using LC/MS Q-TOF. Phytochemical screening, antioxidant activity, cytotoxic tests and metabolites profiling of the respective extracts were carried out in this study. The antiproliferative effects of the crude methanolic extracts of 11 in vitro and wild plant of T. integrifolia were tested for cytotoxic activity against HepG2 cancer cell lines and Chang normal cell lines. The secondary metabolites from plants were extracted using methanol and analysed using LC/MS Q-TOF platform. Principal Component Analysis (PCA), Partial Least Squares Discriminant Analysis (PLS-DA) and Hierarchical Clustering Analysis (HCA) were used to determine differentially expressed metabolites from T. integrifolia in vitro culture and wild plant groups. T. integrifolia were successfully grown using tissue culture techniques. Phytochemical screening confirmed the presence of tannins, triterpenoids, flavonoids, saponins, anthraquinone glycosides, phenols and steroids in the extract of T. integrifolia in vitro plantlet and wild plant extracts. T. integrifolia was rich in high levels of total phenolic and terpenoid compounds. The secondary metabolites profiled include Taccalonolide A, Taccalonolide AA, Betulinic acid, Chlorogenic acid, Dioscin, Diosgenin and Withanolides. These metabolites have been reported to possess several biological activities including antiproliferative activity. The in vitro root extract significantly showed the highest selectivity for its cytotoxic effects in HepG2 compared to normal Chang cell lines. Linoleic acid metabolism was the most prominently perturbated pathway determined in the in vitro root extracts of T. integrifolia with the highest selectivity index towards HepG2 cells. This study has successfully grown T. integrifolia using an in vitro plant culture green technology to produce valuable source of active metabolites with novel selective anti-proliferative properties towards HepG2 cell lines. The findings may suggest that manipulating linoleic acid metabolism of T. integrifolia would allow production of secondary metabolites with selective anti-proliferative activities. Thus, allows the manipulation of the metabolism pathways for production of desired secondary metabolites.