Elicitation strategies of in-vitro cultures for the sustainable use of medicinal plants
Elicitation Strategies of in vitro cultures
Keywords:
F. indica, Callus, Thidiazuron, Anticancer, in vitroAbstract
Medicinal plants are highly traded for its promising potential against different types of diseases including cancers. Development of elicitation strategies for increased production of important anticancer compounds from invitro cultures of medicinal plants has proved very productive. For this purpose, different stresses are applied to invitro cultures to produce increased amounts of the compounds. For instance, cell cultures are produced via stem explants in the Murashige & Skoog basal medium supplemented with different concentrations of plant growth regulators (PGRs). The extracts from samples are then subject to flavonoid and phenolic content assessment, antioxidant quantification and Chromatographic analysis. In our experiments, among the many PGRs, Thidiazuron (TDZ) triggered higher quantities of biomass and total flavonoid & phenolic content (191.03 μg quercetin/mg and 202.8 μg gallic acid equivalent/ mg, respectively) through cell cultures of F. indica. Similarly, sucrose induced the maximum biomass among the different carbon sources (fructose, glucose, maltose, and sucrose) given in different concentrations to cell cultures of F. indica while glucose produced the maximum phenolic content followed by fructose when harvested after 42 days. Manipulation in the supply of light to the cultures with a combined effect from other chemicals, a significant effect was seen on growth and secondary metabolism such that dark-grown cell cultures treated with Methyl Jasmonate (Me-J) gave the highest TPC. High-performance liquid chromatography analysis revealed an increased quantity of secondary metabolites. In conclusion, cell cultures of F. indica treated with Thidiazuron and grown in dark in the presence of glucose as a sugar source and Me-J as elicitor gives enhanced quantities of important anticancer secondary metabolites.
References
Wang, C.Z., T. Calway, & C.S. Yuan. Herbal medicines as adjuvants for cancer therapeutics. Am J Chin Med. 40(4): 657-69 (2012).
Alamgeer, A., Sharif, H. Asif, W. Younis, H. Riaz, I.A. Bukhari, & A.M. Assiri. Indigenous medicinal plants of Pakistan used to treat skin diseases: a review. Chinese medicine. 13: 52-52 (2018).
Shinwari, Z.K. Medicinal plants research in Pakistan. Journal of medicinal plants research. 4(3): 161-176 (2010).
Martín Ortega, A.M. & M.R. Segura Campos. Chapter 13 - Bioactive Compounds as Therapeutic Alternatives, in Bioactive Compounds, M.R.S. Campos, Editor, Woodhead Publishing, p. 247-264 (2019).
Satpute, R.M., R.S. Kashyap, J.Y. Deopujari, H.J. Purohit, G.M. Taori, & H.F. Daginawala. Protection of PC12 cells from chemical ischemia induced oxidative stress by Fagonia arabica. Food and Chemical Toxicology. 47(11): 2689-95 (2009).
Waheed, A., J. Barker, S.J. Barton, C.P. Owen, S. Ahmed, & M.A. Carew. A novel steroidal saponin glycoside from Fagonia indica induces cell-selective apoptosis or necrosis in cancer cells. European Journal of Pharmaceutical Sciences. 47(2): 464-73 (2012).
Greenwell, M. & P.K.S.M. Rahman. Medicinal Plants: Their Use in Anticancer Treatment. International journal of pharmaceutical sciences and research. 6(10): 4103-4112 (2015).
Škrovánková, S., L. Mišurcová, & L. Machů. Chapter Three - Antioxidant Activity and Protecting Health Effects of Common Medicinal Plants, in Advances in Food and Nutrition Research, J. Henry, Editor, Academic Press, p. 75-139 (2012).
DiCosmo, F. & M. Misawa. Plant cell and tissue culture: Alternatives for metabolite production.Biotechnology Advances. 13(3): 425-453 (1995).
Baldi, A. & V.K. Dixit. Yield enhancement strategies for artemisinin production by suspension cultures of Artemisia annua. Bioresourc Technol. 99(11): 4609- 14 (2008).
Murashige, T. & F. Skoog. A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures. Physiologia Plantarum. 15(3): 473-497 (1962).
George, E.F., M.A. Hall, & G.-J.D. Klerk. The Components of Plant Tissue Culture Media I: Macroand Micro-Nutrients, in Plant Propagation by Tissue Culture, E.F. George, M.A. Hall, and G.-J.D. Klerk, Editors, Springer Netherlands: Dordrecht, p. 65-113 (2007).
Chakraborty, N., D. Banerjee, M. Ghosh, P. Pradhan, N.S. Gupta, K. Acharya, & M. Banerjee. Influence of plant growth regulators on callus mediated regeneration and secondary metabolites synthesis in Withania somnifera (L.) Dunal. Physiol Mol Biol Plants. 19(1): 117-25 (2013).
Tognetti, J.A., H.G. Pontis, & G.M. Martinez- Noel. Sucrose signaling in plants: a world yet to be explored. Plant Signal Behav. 8(3): e23316 (2013).
Wind, J., S. Smeekens, & J. Hanson. Sucrose: metabolite and signaling molecule. Phytochemistry. 71(14-15): 1610-4 (2010).
Kumar, G.P., S. Subiramani, S. Govindarajan, V. Sadasivam, V. Manickam, K. Mogilicherla, S.K. Thiruppathi, & J. Narayanasamy. Evaluation of different carbon sources for high frequency callus culture with reduced phenolic secretion in cotton (Gossypium hirsutum L.) cv. SVPR-2. Biotechnology Reports. 7: 72-80 (2015).
Niedz, R.P. & T.J. Evens. The effects of nitrogen and potassium nutrition on the growth of nonembryogenic and embryogenic tissue of sweet orange (Citrus sinensis (L.) Osbeck). BMC Plant Biology. 8(1): 126 (2008).
Nell, M., M. Vötsch, H. Vierheilig, S. Steinkellner, K. Zitterl-Eglseer, C. Franz, & J. Novak. Effect of phosphorus uptake on growth and secondary metabolites of garden sage (Salvia officinalis L.). Journal of the Science of Food and Agriculture. 89(6): 1090-1096 (2009).
Praveen, N. & H. Murthy. Withanolide A production from Withania somnifera hairy root cultures with improved growth by altering the concentrations of macro elements and nitrogen source in the medium. Acta physiologiae plantarum. 35(3): 811-816 (2013).
Murthy, H.N., E.-J. Lee, & K.-Y. Paek. Production of secondary metabolites from cell and organ cultures: strategies and approaches for biomass improvement and metabolite accumulation. Plant Cell, Tissue and Organ Culture. 118(1): 1-16 (2014).
Abdolzadeh, A., X. Wang, E.J. Veneklaas, & H. Lambers. Effects of phosphorus supply on growth, phosphate concentration and cluster-root formation in three Lupinus species. Annals of Botany. 105(3): 365-74 (2010).
Nagella, P. & H.N. Murthy. Effects of macroelements and nitrogen source on biomass accumulation and withanolide-A production from cell suspension cultures of Withania somnifera (L.) Dunal. Plant Cell, Tissue and Organ Culture. 104(1): 119-124 (2010).
Ramachandra Rao, S. & G.A. Ravishankar. Plant cell cultures: Chemical factories of secondary metabolites. Biotechnology Advances. 20(2): 101- 153 (2002).
Ljung, K. Auxin metabolism and homeostasis during plant development. Development. 140(5): 943-50 (2013).
Kadota, M. & Y. Niimi. Effects of cytokinin types and their concentrations on shoot proliferation and hyperhydricity in in-vitro pear cultivar shoots. Plant Cell, Tissue and Organ Culture. 72(3): 261-265 (2003).
Polanco, M.C. & M.L. Ruiz. Effect of benzylaminopurine on in-vitro and in vivo root development in lentil, Lens culinaris Medik. Plant Cell Reports. 17(1): 22-26 (1997).
Dobrev, P.I., K. Hoyerová, & J. Petrášek. Analytical Determination of Auxins and Cytokinins, in Auxins and Cytokinins in Plant Biology: Methods and Protocols, T. Dandekar and M. Naseem, Editors, Springer New York: New York, NY, p. 31-39 (2017).
Saeed, T. & A. Shahzad. High frequency plant regeneration in Indian Siris via cyclic somatic embryogenesis with biochemical, histological and SEM investigations. Ind Crops Prod. 76: 623-637 (2015).
Shahzad, A., S. Sharma, S. Parveen, T. Saeed, A. Shaheen, R. Akhtar, V. Yadav, A. Upadhyay, & Z. Ahmad. Historical Perspective and Basic Principles of Plant Tissue Culture, in Plant Biotechnology: Principles and Applications, M.Z. Abdin, et al.,Editors, Springer Singapore: Singapore, p. 1-36 (2017).
Saeed, S., H. Ali, T. Khan, W. Kayani, & M.A. Khan. Impacts of methyl jasmonate and phenyl acetic acid on biomass accumulation and antioxidant potential in adventitious roots of Ajuga bracteosa Wall ex Benth., a high valued endangered medicinal plant. Physiology and Molecular Biology of Plants. 23(1):229-237 (2017).
Liang, Z., Y. Ma, T. Xu, B. Cui, Y. Liu, Z. Guo, & D. Yang. Effects of abscisic acid, gibberellin, ethylene and their interactions on production of phenolic acids in Salvia miltiorrhiza bunge hairy roots. PloS one. 8(9): e72806 (2013).
Naikawadi, V.B., M.L. Ahire, A. Lahiri, & T.D. Nikam. In-vitro propagation and cell cultures of memory tonic herb Evolvulus alsinoides: a best source for elicited production of scopoletin. Applied Microbiology and Biotechnology. 100(8): 3463-76 (2016).
Amoo, S.O. & J. Van Staden. Influence of plant growth regulators on shoot proliferation and secondary metabolite production in micropropagated Huernia hystrix. Plant Cell, Tissue and Organ Culture. 112(2): 249-256 (2012).
Murthy, B.N.S., S.J. Murch, & P.K. Saxena. Thidiazuron: A potent regulator of in-vitro plant morphogenesis. In Vitro Cellular & Developmental Biology - Plant. 34(4): 267-275 (1998).
Jones, M.P., Z. Yi, S.J. Murch, & P.K. Saxena. Thidiazuron-induced regeneration of Echinacea purpurea L.: micropropagation in solid and liquid culture systems. Plant Cell Reports. 26(1): 13-9 (2007).
Guo, B., B.H. Abbasi, A. Zeb, L. Xu, & Y. Wei. Thidiazuron: a multi-dimensional plant growth regulator. Afr J Biotechnol. 10(45): 8984-9000 (2011).
Ali, M. & B.H. Abbasi. Thidiazuron-induced changes in biomass parameters, total phenolic content, and antioxidant activity in callus cultures of Artemisia absinthium L. Applied Biochemistry and Biotechnology. 172(5): 2363-76 (2014).
Thiruvengadam, M. & I.M. Chung. Phenolic compound production and biological activities from in-vitro regenerated plants of gherkin (Cucumis anguria L.). Electronic Journal of Biotechnology. 18(4): 295-301 (2015).
Karam, N.S., F.M. Jawad, N.A. Arikat, & R.A. Shibl. Growth and rosmarinic acid accumulation in callus, cell suspension, and root cultures of wild Salvia fruticosa. Plant Cell, Tissue and Organ Culture. 73(2): 117-121 (2003).
Teoh, E.S. Secondary Metabolites of Plants, in Medicinal Orchids of Asia, Springer International Publishing: Cham, p. 59-73 (2016).
Baenas, N., C. Garcia-Viguera, & D.A. Moreno. Elicitation: a tool for enriching the bioactive composition of foods. Molecules. 19(9): 13541-63 (2014).
Ghorbanpour, M. & J. Hadian. Multi-walled carbon nanotubes stimulate callus induction, secondary metabolites biosynthesis and antioxidant capacity in medicinal plant Satureja khuzestanica grown invitro. Carbon. 94: 749-759 (2015).
Gundlach, H., M.J. Müller, T.M. Kutchan, & M.H. Zenk. Jasmonic acid is a signal transducer in elicitor-induced plant cell cultures. Proc Natl Acad Sci USA. 89(6): 2389-2393 (1992).
Ramirez-Estrada, K., H. Vidal-Limon, D. Hidalgo, E. Moyano, M. Golenioswki, R.M. Cusido, & J. Palazon. Elicitation, an Effective Strategy for the Biotechnological Production of Bioactive High- Added Value Compounds in Plant Cell Factories. Molecules. 21(2): 182 (2016).
Thanh, N.T., H.N. Murthy, K.W. Yu, E.J. Hahn, & K.Y. Paek. Methyl jasmonate elicitation enhanced synthesis of ginsenoside by cell suspension cultures of Panax ginseng in 5-l balloon type bubble bioreactors. Appl Microbiol Biotechnol. 67(2): 197-201 (2005).
Kim, Y.S., E.C. Yeung, E.J. Hahn, & K.Y. Paek. Combined effects of phytohormone, indole-3-butyric acid, and methyl jasmonate on root growth and ginsenoside production in adventitious root cultures of Panax ginseng C.A. Meyer. Biotechnology Letters. 29(11): 1789-92 (2007).
Wang, J., W. Gao, B. Zuo, L. Zhang, & L. Huang. Effect of methyl jasmonate on the ginsenoside content of Panax ginseng adventitious root cultures and on the genes involved in triterpene biosynthesis. Research on Chemical Intermediates. 39(5): 1973-1980 (2012).
Nacif de Abreu, I. & P. Mazzafera. Effect of water and temperature stress on the content of active constituents of Hypericum brasiliense Choisy. Plant Physiology and Biochemistry. 43(3): 241-8 (2005).
Zobayed, S.M., F. Afreen, & T. Kozai. Temperature stress can alter the photosynthetic efficiency and secondary metabolite concentrations in St. John’s wort. Plant Physiology and Biochemistry. 43(10-11): 977-84 (2005).
Shin, K.S., H.N. Murthy, J.W. Heo, E.J. Hahn, & K.Y. Paek. The effect of light quality on the growth and development of in-vitro cultured Doritaenopsis plants. Acta Physiologiae Plantarum. 30(3): 339-343 (2008).
Shohael, A.M., M.B. Ali, K.W. Yu, E.J. Hahn, R. Islam, & K.Y. Paek. Effect of light on oxidative stress, secondary metabolites and induction of antioxidant enzymes in Eleutherococcus senticosus somatic embryos in bioreactor. Process Biochemistry. 41(5): 1179-1185 (2006).
Zoratti, L., K. Karppinen, A. Luengo Escobar, H. Haggman, & L. Jaakola. Light-controlled flavonoid biosynthesis in fruits. Front Plant Sci. 5: 534 (2014).
Khan, M.A., B.H. Abbasi, N. Ahmed, & H. Ali. Effects of light regimes on in-vitro seed germination cand silymarin content in Silybum marianum. Ind Crops Prod. 46: 105-110 (2013).
Abbasi, B.H., C.L. Tian, S.J. Murch, P.K. Saxena, & C.Z. Liu. Light-enhanced caffeic acid derivatives biosynthesis in hairy root cultures of Echinacea purpurea. Plant Cell Reports. 26(8): 1367-72 (2007).
Ali, M. & B.H. Abbasi. Light-induced fluctuations in biomass accumulation, secondary metabolites production and antioxidant activity in cell suspension cultures of Artemisia absinthium L. Journal of Photochemistry and Photobiology B: Biology. 140: 223-7 (2014).
Anjum, S., B.H. Abbasi, J. Doussot, A. Favre- Reguillon, & C. Hano. Effects of photoperiod regimes and ultraviolet-C radiations on biosynthesis of industrially important lignans and neolignans in cell cultures of Linum usitatissimum L. (Flax). Journal of Photochemistry and Photobiology B:Biology. 167: 216-227 (2017).
Ahmad, N., B.H. Abbasi, H. Fazal, M.A. Khan, & M.S. Afridi. Effect of reverse photoperiod on invitro regeneration and piperine production in Piper nigrum L. Comptes Rendus Biologies. 337(1): 19-28 (2014).
Fazal, H., B.H. Abbasi, N. Ahmad, S.S. Ali, F.Akbar, & F. Kanwal. Correlation of different spectral lights with biomass accumulation and production of antioxidant secondary metabolites in callus cultures of medicinally important Prunella vulgaris L. Journal of Photochemistry and Photobiology B: Biology. 159: 1-7 (2016).
Tariq, U., M. Ali, & B.H. Abbasi. Morphogenic and biochemical variations under different spectral lights in callus cultures of Artemisia absinthium L. Journal of Photochemistry and Photobiology B: Biology. 130: 264-71 (2014).
Published
How to Cite
Issue
Section
License
Creative Commons Attribution (CC BY). Allows users to: copy the article and distribute; abstracts, create extracts, and other revised versions, adaptations or derivative works of or from an article (such as a translation); include in a collective work (such as an anthology); and text or data mine the article. These uses are permitted even for commercial purposes, provided the user: includes a link to the license; indicates if changes were made; gives appropriate credit to the author(s) (with a link to the formal publication through the relevant DOI); and does not represent the author(s) as endorsing the adaptation of the article or modify the article in such a way as to damage the authors' honor or reputation.