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Biotechnology

Year: 2023 | Volume: 22 | Issue: 1 | Page No.: 1-17
DOI: 10.3923/biotech.2023.1.17

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Review Article

In vitro Production of Plant Nutraceuticals

Sahwky Bekheet
Department of Plant Biotechnology, National Research Centre, 33 El Buhouth Street, Dokki 12622, Giza, Egypt
LiveDNA: 20.16991

Valbona Sota
Department of Biotechnology, Faculty of Natural Sciences, University of Tirana, Tirana, Albania

Biotechnology methods particularly tissue culture techniques offer new approaches for the in vitro production of valuable plant nutraceuticals. The large-scale production of secondary metabolites in a year-round system without seasonal constraints is one of the advantages of plant tissue culture techniques. Furthermore, enhancement of in vitro nutraceuticals production can be realized by a selection of high-producing cell lines and medium optimization. In this respect, several techniques have been adopted to improve the production of plant-derived nutraceuticals such as mutation, elicitation, precursor feeding, genetic transformation and metabolic engineering. In vitro mutagenesis of cultured cells and tissues by irradiation or chemical mutagens represents a feasible method for the improvement of nutraceuticals production. Likewise, transformation is another strategy that is used to enhance nutraceuticals in plant cells or organ tissues. At this point, hairy root culture induced by Agrobacterium rhizogenes is the most promising transformation technique used for in vitro production of valuable plant compounds. The benefits of hairy roots are high metabolite productivity, high growth rates and inherent genetic stability. On the other hand, due to its effectiveness and practical feasibility, elicitation is considered the most applied strategy for enhancing the production of desired compounds in plant biotechnology. Biotic (biological origin) and abiotic (non-biological origin) elicitors are used to increase the production of plant metabolites by different effects on the cellular processes in the plant system. Furthermore, bioreactors developed for in vitro industrial-scale production of desired compounds can be used for continuous and scaling-up plant nutraceuticals production. This article discusses different aspects of biotechnology used for the selection and enhancement production of nutraceuticals from plant cultures grown cells, in vitro.


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How to cite this article

Sahwky Bekheet and Valbona Sota, 2023. In vitro Production of Plant Nutraceuticals. Biotechnology, 22: 1-17.

DOI: 10.3923/biotech.2023.1.17

URL: https://scialert.net/abstract/?doi=biotech.2023.1.17

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References


  1. Hardy, G., 2000. Nutraceuticals and functional foods: Introduction and meaning. Nutrition, 16: 688-689.
    CrossRefPubMedDirect Link

  2. Kwak, N.S. and D.J. Jukes, 2001. Functional foods. Part 2: The impact on current regulatory terminology. Food Control, 12: 109-117.
    CrossRefDirect Link

  3. Biesalski, H.K., L.O. Dragsted, I. Elmadfa, R. Grossklaus and M. Müller et al., 2009. Bioactive compounds: Definition and assessment of activity. Nutrition, 25: 1202-1205.
    CrossRefDirect Link

  4. Nasri, H., A. Baradaran, H. Shirzad and M. Rafieian-Kopaei, 2014. New concepts in nutraceuticals as alternative for pharmaceuticals. Int. J. Preventive Med., 5: 1487-1499.
    Direct Link

  5. Elless, M.P., M.J. Blaylock, J.W. Huang and C.D. Gussman, 2000. Plants as a natural source of concentrated mineral nutritional supplements. Food Chem., 71: 181-188.
    CrossRefDirect Link

  6. Liu, H., N. Qiu, H. Ding and R. Yao, 2008. Polyphenols contents and antioxidant capacity of 68 Chinese herbals suitable for medical or food uses. Food Res. Int., 41: 363-370.
    CrossRefDirect Link

  7. Lucock, M., 2004. Is folic acid the ultimate functional food component for disease prevention? BMJ, 328: 211-214.
    CrossRefDirect Link

  8. Siddhuraju, P. and K. Becker, 2007. The antioxidant and free radical scavenging activities of processed cowpea (Vigna unguiculata (L.) Walp.) seed extracts. Food Chem., 101: 10-19.
    CrossRefDirect Link

  9. Halder, M., D. Roychowdhury and S. Jha, 2018. A Critical Review on Biotechnological Interventions for Production and Yield Enhancement of Secondary Metabolites in Hairy Root Cultures. In: Hairy Roots: An Effective Tool of Plant Biotechnology, Srivastava, V., S. Mehrotra and S. Mishra (Eds.), Springer, Singapore, ISBN: 978-981-13-2561-8, pp: 21-44.
    CrossRefDirect Link

  10. Buttriss, J.L. and C.S. Stokes, 2008. Dietary fibre and health: An overview. Nutr. Bull., 33: 186-200.
    CrossRefDirect Link

  11. Bingham, S.A., N.E. Day, R. Luben, P. Ferrari and N. Slimani et al., 2003. Dietary fibre in food and protection against colorectal cancer in the European prospective investigation into cancer and nutrition (EPIC): An observational study. Lancet, 361: 1496-1501.
    CrossRefPubMedDirect Link

  12. Rodiño-Janeiro, B.K., M. Vicario, C. Alonso-Cotoner, R. Pascua-García and J. Santos, 2018. A review of microbiota and irritable bowel syndrome: Future in therapies. Adv. Ther., 35: 289-310.
    CrossRefDirect Link

  13. Delgado, G.T.C., W.M. da Silva Cunha Tamashiro, M.R. Marostica Jr., Y.M.F. Moreno and G.M. Pastore, 2011. The putative effects of prebiotics as immunomodulatory agents. Food Res. Int., 44: 3167-3173.
    CrossRefDirect Link

  14. Simopoulos, A.P., 2016. An increase in the omega-6/omega-3 fatty acid ratio increases the risk for obesity. Nutrients, Vol. 8.
    CrossRefDirect Link

  15. Kurutas, E.B., 2015. The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: Current state. Nutr. J., Vol. 15.
    CrossRefDirect Link

  16. Youdim, K.A. and J.A. Joseph, 2001. A possible emerging role of phytochemicals in improving age-related neurological dysfunctions: A multiplicity of effects. Free Radical Biol. Med., 30: 583-594.
    CrossRefDirect Link

  17. Dzialo, M., J. Mierziak, U. Korzun, M. Preisner, J. Szopa and A. Kulma, 2016. The potential of plant phenolics in prevention and therapy of skin disorders. Int. J. Mol. Sci., Vol. 17.
    CrossRefDirect Link

  18. Panche, A.N., A.D. Diwan and S.R. Chandra, 2016. Flavonoids: An overview. J. Nutr. Sci., Vol. 5.
    CrossRefDirect Link

  19. Kaefer, C.M. and J.A. Milner, 2008. The role of herbs and spices in cancer prevention. J. Nutr. Biochem., 19: 347-361.
    CrossRefDirect Link

  20. Thakur, A. and R. Sharma, 2018. Health promoting phytochemicals in vegetables: A mini review. Int. J. Food Ferment. Technol., 8: 107-117.
    Direct Link

  21. Das, L., E. Bhaumik, U. Raychaudhuri and R. Chakraborty, 2012. Role of nutraceuticals in human health. J. Food Sci. Technol., 49: 173-183.
    CrossRefDirect Link

  22. Tholl, D., 2006. Terpene synthases and the regulation, diversity and biological roles of terpene metabolism. Curr. Opin. Plant Biol., 9: 297-304.
    CrossRefPubMedDirect Link

  23. Dillard, C.J. and J.B. German, 2000. Phytochemicals: Nutraceuticals and human health. J. Sci. Food Agric., 80: 1744-1756.
    CrossRefDirect Link

  24. Kline, K., W. Yu and B.G. Sanders, 2004. Vitamin E and breast cancer. J. Nutr., 134: 3458S-3462S.
    CrossRefDirect Link

  25. Milani, A., M. Basirnejad, S. Shahbazi and A. Bolhassani, 2017. Carotenoids: Biochemistry, pharmacology and treatment. Br. J. Pharmacol., 174: 1290-1324.
    CrossRefDirect Link

  26. D'Archivio, M., C. Filesi, R. Vari, B. Scazzocchio and R. Masella, 2010. Bioavailability of the polyphenols: Status and controversies. Int. J. Mol. Sci., 11: 1321-1342.
    CrossRefDirect Link

  27. Crozier, A., I.B. Jaganath and M.N. Clifford, 2009. Dietary phenolics: Chemistry, bioavailability and effects on health. Nat. Prod. Rep., 26: 1001-1043.
    CrossRefDirect Link

  28. Yao, L.H., Y.M. Jiang, J. Shi, F.A.Tomás-Barberán, N. Datta, R. Singanusong and S.S. Chen, 2004. Flavonoids in food and their health benefits. Plant Foods Hum. Nutr., 59: 113-122.
    CrossRefDirect Link

  29. Escarpa, A. and M.C. Gonzalez, 2001. Approach to the content of total extractable phenolic compounds from different food samples by comparison of chromatographic and spectrophotometric methods. Anal. Chim. Acta, 427: 119-127.
    CrossRefDirect Link

  30. Kuete, V., H. Fouotsa, A.T. Mbaveng, B. Wiench, A.E. Nkengfack and T. Efferth, 2015. Cytotoxicity of a naturally occurring furoquinoline alkaloid and four acridone alkaloids towards multi-factorial drug-resistant cancer cells. Phytomedicine, 22: 946-951.
    CrossRefDirect Link

  31. Traka, M. and R. Mithen, 2009. Glucosinolates, isothiocyanates and human health. Phytochem. Rev., 8: 269-282.
    CrossRefDirect Link

  32. Ashihara, H., H. Sano and A. Crozier, 2008. Caffeine and related purine alkaloids: Biosynthesis, catabolism, function and genetic engineering. Phytochemistry, 69: 841-856.
    CrossRefDirect Link

  33. Brufaua, G., M.A. Canelab and M. Rafecasa, 2008. Phytosterols: Physiologic and metabolic aspects related to cholesterol-lowering properties. Nutr. Res., 28: 217-225.
    CrossRefDirect Link

  34. Sharma, R., S. Kumar, V. Kumar and A. Thakur, 2019. Comprehensive review on nutraceutical significance of phytochemicals as functional food ingredients for human health management. J. Pharmacogn. Phytochem., 8: 385-395.
    CrossRefDirect Link

  35. Grattan, B.J., 2013. Plant sterols as anticancer nutrients: Evidence for their role in breast cancer. Nutrients, 5: 359-387.
    CrossRefDirect Link

  36. Kamal-Eldin, A. and A. Moazzami, 2009. Plant sterols and stanols as cholesterol-lowering ingredients in functional foods. Recent Pat. Food Nutr. Agric., 1: 1-14.
    CrossRefDirect Link

  37. Woyengo, T.A., V.R. Ramprasath and P.J.H. Jones, 2009. Anticancer effects of phytosterols. Eur. J. Clin. Nutr., 63: 813-820.
    CrossRefDirect Link

  38. Peinado, M.J., R. Ruiz, A. Echávarri and L.A. Rubio, 2012. Garlic derivative propyl propane thiosulfonate is effective against broiler enteropathogens in vivo. Poult. Sci., 91: 2148-2157.
    CrossRefDirect Link

  39. Torres-Palazzolo, C., D. Ramirez, D. Locatelli, W. Manucha, C. Castro and A. Camargo, 2018. Bioaccessibility and permeability of bioactive compounds in raw and cooked garlic. J. Food Compos. Anal., 70: 49-53.
    CrossRefDirect Link

  40. Pylypets, A.Z., R.Y. Iskra, V.V. Havryliak, A.V. Nakonechna, V.P. Novikov and V.I. Lubenets, 2017. Effects of thiosulfonates on the lipid composition of rat tissues. Ukr. Biochem. J., 89: 56-62.
    CrossRefDirect Link

  41. Rao, P.S.S., N.M. Midde, D.D. Miller, S. Chauhan, A. Kumar and S. Kumar, 2015. Diallyl sulfide: Potential use in novel therapeutic interventions in alcohol, drugs, and disease mediated cellular toxicity by targeting cytochrome P450 2E1. Curr. Drug Metab., 16: 486-503.
    CrossRefDirect Link

  42. Karuppusamy, S., 2009. A review on trends in production of secondary metabolites from higher plants by in vitro tissue, organ and cell cultures. J. Med. Plants Res., 3: 1222-1239.
    CrossRefDirect Link

  43. Taha, H.S., S.A. Bekheet and M.K. El-Bahr, 2012. A new concept for production and scaling up of bioactive compounds from Egyptian date palm (Zaghlool) cultivar using bioreactor. Emir. J. Food Agric., 24: 425-433.
    Direct Link

  44. Gabr, A.M.M., H. Ghareeb, H.M. El Shabrawi, I. Smetanska and S.A. Bekheet, 2016. Enhancement of silymarin and phenolic compound accumulation in tissue culture of milk thistle using elicitor feeding and hairy root cultures. J. Genet. Eng. Biotechnol., 14: 327-333.
    CrossRefDirect Link

  45. Dhiman, N., V. Patial and A. Bhattacharya, 2018. The Current Status and Future Applications of Hairy Root Cultures. In: Biotechnological Approaches for Medicinal and Aromatic Plants, Kumar, N. (Ed.), Springer, Singapore, ISBN 978-981-13-0534-4, pp: 87-155.
    CrossRefDirect Link

  46. Hidalgo, D., R. Sanchez, L. Lalaleo, M. Bonfill, P. Corchete and J. Palazon, 2018. Biotechnological production of pharmaceuticals and biopharmaceuticals in plant cell and organ cultures. Curr. Med. Chem., 25: 3577-3596.
    CrossRefDirect Link

  47. Gutierrez-Valdes, N., S.T. Häkkinen, C. Lemasson, M. Guillet, K.M. Oksman-Caldentey, A. Ritala and F. Cardon, 2020. Hairy root cultures-A versatile tool with multiple applications. Front. Plant Sci., Vol. 11.
    CrossRefDirect Link

  48. Wang, P., E. Lombi, F.J. Zhao and P.M. Kopittke, 2016. Nanotechnology: A new opportunity in plant sciences. Trends Plant Sci., 21: 699-712.
    CrossRefDirect Link

  49. Almusawi, A.H.A., A.J. Sayegh, A.M. Alshanaw and J.L. Griffis, 2017. Plantform Bioreactor for Mass Micropropagation of Date Palm. In: Date Palm Biotechnology Protocols, Al-Khayri, J.M., S.M. Jain and D.V. Johnson (Eds.), Humana Press, New York, US, ISBN: 978-1-4939-7156-5, pp: 251-265.
    CrossRefDirect Link

  50. Alamgir, A.N.M., 2017. Therapeutic Use of Medicinal Plants and Their Extracts: Volume 1. 1st Edn., Springer, Cham, Switzerland, ISBN: 978-3-319-63862-1, Pages: 546.
    CrossRefDirect Link

  51. Menin, B., A. Moglia, C. Comino, J.C. Hakkert, S. Lanteri and J. Beekwilder, 2013. In vitro callus-induction in globe artichoke (Cynara cardunculus L. var. scolymus) as a system for the production of caffeoylquinic acids. J. Hortic. Sci. Biotechnol., 88: 537-542.
    CrossRefDirect Link

  52. Ibrahim, M.M., M.K. El-Bahr and M.R. Rady, 2019. In-vitro adventitious root production of Cichorium endivia L. and antioxidants, total phenolic, and total flavonoids assessments. Egypt. Pharm. J., 18: 216-227.
    CrossRefDirect Link

  53. Ibrahim, M.M., M.M. Mounier and S.A. Bekheet, 2019. Glucosinolates constituents and cytotoxic activities of Lepidium sativum L. callus cultures. J. Environ. Sci. Technol., 12: 138-148.
    CrossRefDirect Link

  54. Grace, S.C. and B.A. Logan, 2000. Energy dissipation and radical scavenging by the plant phenylpropanoid pathway. Philos. Trans. R. Soc. B. Biol. Sci., 355: 1499-1510.
    CrossRefDirect Link

  55. Nazif, N.M., M.R. Rady and M.S. El-Nasr, 2000. Stimulation of anthraquinone production in suspension cultures of Cassia acutifolia by salt stress. Fitoterapia, 71: 34-40.
    CrossRefDirect Link

  56. Chutipaijit, S., S. Cha-Um and K. Sompornpailin, 2009. Differential accumulations of praline and flavonoids in indica rice varieties against salinity. Pak. J. Bot., 41: 2497-2506.
    Direct Link

  57. Chan, L.K., S.S. Koay, P.L. Boey and A. Bhatt, 2010. Effects of abiotic stress on biomass and anthocyanin production in cell cultures of Melastoma malabathricum. Biol. Res., 43: 127-135.
    CrossRefDirect Link

  58. El-Shabrawi, H.M., H.E. Wahba, A.M. Gabr, S.I. El-Morsy, M.A. Saber and S.A. Bekheet, 2019. Improvement of wax oil content of embryonic callus of jojoba using gamma radiation. Plant Tissue Culture Biotechnol., 29: 207-217.
    CrossRefDirect Link

  59. Mba, C., 2013. Induced mutations unleash the potentials of plant genetic resources for food and agriculture. Agronomy, 3: 200-231.
    CrossRefDirect Link

  60. Yamaguchi, H., S. Nagatomi, T. Morishita, K. Degi, A. Tanaka, N. Shikazono and Y. Hase, 2003. Mutation induced with ion beam irradiation in rose. Nucl. Instrum. Methods Phys. Res., Sect. B: Beam Interact. Mater. Atoms, 206: 561-564.
    CrossRefDirect Link

  61. Wi, S.G., B.Y. Chung, J.H. Kim, M.H. Baek, D.H. Yang, J.W. Lee and J.S. Kim, 2005. Ultrastructural changes of cell organelles in Arabidopsis stems after gamma irradation. J. Plant Biol., 48: 195-200.
    CrossRefDirect Link

  62. Kim, D.S., S.Y. Kim, I.Y. Jeong, J.B. Kim, G.J. Lee, S.Y. Kang and W. Kim, 2009. Improvement of ginsenoside production by Panax ginseng adventitious roots induced by γ-irradiation. Biol. Plant. 53: 408-414.
    CrossRefDirect Link

  63. Kim, D.S., M. Song, S.H. Kim, D.S. Jang and J.B. Kim et al., 2013. The improvement of ginsenoside accumulation in Panax ginseng as a result of γ-irradiation. J. Ginseng Res., 37: 332-340.
    CrossRefDirect Link

  64. Patil, A.S., P. Suryavanshi and D. Fulzele, 2018. Evaluation of effect of gamma radiation on total phenolic content, flavonoid and antioxidant activity of in vitro callus culture of Artemisia annua. Nat. Prod. Chem. Res., Vol. 6.
    CrossRefDirect Link

  65. Chung, B.Y., Y.B. Lee, M.H. Baek, J.H. Kim, S.G. Wi and J.S. Kim, 2006. Effects of low-dose gamma-irradiation on production of shikonin derivatives in callus cultures of Lithospermum erythrorhizon S. Radiat. Phys. Chem., 75: 1018-1023.
    CrossRefDirect Link

  66. El-Beltagi, H.S., O.K. Ahmed and W. El-Desouky, 2011. Effect of low doses γ-irradiation on oxidative stress and secondary metabolites production of rosemary (Rosmarinus officinalis L.) callus culture. Radiat. Phys. Chem., 80: 968-976.
    CrossRefDirect Link

  67. Khalil, S.A., N. Ahmad and R. Zamir, 2015. Gamma radiation induced variation in growth characteristics and production of bioactive compounds during callogenesis in Stevia rebaudiana (Bert.) New Neg. Plant Sci., 1-2: 1-5.
    CrossRefDirect Link

  68. Kim, J.H., B.Y. Chung, J.S. Kim and S.G. Wi, 2005. Effects of in Planta gamma-irradiation on growth, photosynthesis and antioxidative capacity of red pepper (Capsicum annuum L.) plants. J. Plant Biol., 48: 47-56.
    CrossRefDirect Link

  69. Goyal, S., M.R. Wani and S. Khan, 2019. Frequency and spectrum of chlorophyll mutations induced by single and combination treatments of gamma rays and EMS in urdbean. Asian J. Biol. Sci., 12: 156-163.
    CrossRefDirect Link

  70. Nicoloff, H., 1974. Effects of sodium acetate and sodium chloride on EMS-induced chlorophyll mutations in barley. Mutat. Res. Fundam. Mol. Mech. Mutagen., 23: 57-62.
    CrossRefDirect Link

  71. Mostafa, G.G., 2015. Effect of some chemical mutagens on the growth, phytochemical composition and induction of mutations in Khaya senegalensis. Int. J. Plant Breed. Genet., 9: 57-67.
    CrossRefDirect Link

  72. Shah, D., A.N. Kamili, A.A. Wani, U. Majeed, Z.A. Wani, N. Sajjad and P. Ahmad, 2020. Promoting the accumulation of scopolamine and hyoscyamine in Hyoscyamus niger L. through EMS based mutagenesis. PLoS ONE, Vol. 15.
    CrossRefDirect Link

  73. Kumar, G. and A. Pandey, 2019. Ethyl methane sulphonate induced changes in cyto-morphological and biochemical aspects of Coriandrum sativum L. J. Saudi Soc. Agric. Sci., 18: 469-475.
    CrossRefDirect Link

  74. Kim, Y.S., E.J. Hahn, H.N. Murthy and K.Y. Paek, 2004. Adventitious root growth and ginsenoside accumulation in Panax ginseng cultures as affected by methyl jasmonate. Biotechnol. Lett., 26: 1619-1622.
    CrossRefPubMedDirect Link

  75. Inthima, P. and K. Sujipuli, 2019. Improvement of growth and bacoside production in Bacopa monnieri through induced autotetraploidy with colchicine. Peer J., Vol. 7.
    CrossRefDirect Link

  76. Wang, L.J., M.Y. Sheng, P.C. Wen and J.Y. Du, 2017. Morphological, physiological, cytological and phytochemical studies in diploid and colchicine-induced tetraploid plants of Fagopyrum tataricum (L.) Gaertn. Bot. Stud., Vol. 58.
    CrossRefDirect Link

  77. Hidalgo, D., M. Georgiev, A. Marchev, R. Bru-Martínez, R.M. Cusido, P. Corchete and J. Palazon, 2017. Tailoring tobacco hairy root metabolism for the production of stilbenes. Sci. Rep., Vol. 7.
    CrossRefDirect Link

  78. Gális, I., Y. Kakiuchi, P. Simek and H. Wabiko, 2004. Agrobacterium tumefaciens AK-6b gene modulates phenolic compound metabolism in tobacco. Phytochemistry, 65: 169-179.
    CrossRefDirect Link

  79. Bulgakov, V.P., 2008. Functions of rol genes in plant secondary metabolism. Biotechnol. Adv., 26: 318-324.
    CrossRefDirect Link

  80. Srivastava, S. and A.K. Srivastava, 2007. Hairy root culture for mass-production of high-value secondary metabolites. Crit. Rev. Biotechnol., 27: 29-43.
    CrossRefDirect Link

  81. Sevón, N. and K.M. Oksman-Caldentey, 2002. Agrobacterium rhizogenes-mediated transformation: Root cultures as a source of alkaloids. Planta Med., 68: 859-868.
    CrossRefPubMedDirect Link

  82. Veena, V. and C.G. Taylor, 2007. Agrobacterium rhizogenes: Recent developments and promising applications. In vitro Cell. Dev. Biol. Plant, 43: 383-403.
    CrossRefDirect Link

  83. Vojin, T., M. Snežana, C. Aleksandar, P. Marija and T. Milana et al., 2014. Production of hairy root cultures of lettuce (Lactuca sativa L.). Cent. Eur. J. Biol., 9: 1196-1205.
    CrossRefDirect Link

  84. Ismail, H., E. Dilshad, M.T. Waheed, M. Sajid, W.K. Kayani and B. Mirza, 2016. Transformation of Lactuca sativa L. with rol C gene results in increased antioxidant potential and enhanced analgesic, anti-inflammatory and antidepressant activities in vivo. 3 Biotech, Vol. 6.
    CrossRefDirect Link

  85. Christey, M.C. and R.H. Braun, 2005. Production of Hairy Root Cultures and Transgenic Plants by Agrobacterium rhizogenes-Mediated Transformation. In: Transgenic Plants: Methods and Protocols. Methods in Molecular Biology, Peña, L. (Ed.), Humana Press, United States, ISBN: 978-1-59259-827-4, pp: 47-60.
    CrossRefDirect Link

  86. Georgiev, M.I., A.I. Pavlov and T. Bley, 2007. Hairy root type plant in vitro systems as sources of bioactive substances. Appl. Microbiol. Biotechnol., 74: 1175-1185.
    CrossRefDirect Link

  87. Chandra, S. and R. Chandra, 2011. Engineering secondary metabolite production in hairy roots. Phytochem. Rev., 10: 371-395.
    CrossRefDirect Link

  88. Ismail, H., E. Dilshad, M.T. Waheed and B. Mirza, 2017. Transformation of lettuce with rol ABC genes: Extracts show enhanced antioxidant, analgesic, anti-inflammatory, antidepressant, and anticoagulant activities in rats. Appl. Biochem. Biotechnol., 181: 1179-1198.
    CrossRefDirect Link

  89. Chung, I.M., M. Thiruvengadam, K. Rekha and G. Rajakumar, 2016. Elicitation enhanced the production of phenolic compounds and biological activities in hairy root cultures of bitter melon (Momordica charantia L.). Braz. Arch. Biol. Technol., Vol. 59.
    CrossRefDirect Link

  90. Kiselev, K.V., A.S. Dubrovina, M.V. Veselova, V.P. Bulgakov, S.A. Fedoreyev and Y.N. Zhuravlev, 2007. The rolB gene-induced overproduction of resveratrol in Vitis amurensis transformed cells. J. Biotechnol., 128: 681-692.
    CrossRefDirect Link

  91. Kim, Y.K., X. Li, H. Xu, N.I. Park, M.R. Uddin, J.Y. Pyon and S.U. Park, 2009. Production of phenolic compounds in hairy root culture of tartary buckwheat (Fagopyrum tataricum Gaertn). J. Crop Sci. Biotechnol., 12: 53-57.
    CrossRefDirect Link

  92. Zhu, C., S. Naqvi, S. Gomez-Galera, A.M. Pelacho, T. Capell and P. Christou, 2007. Transgenic strategies for the nutritional enhancement of plants. Trends Plant Sci., 12: 548-555.
    CrossRefDirect Link

  93. Ruiz-Lopez, N., O. Sayanova, J.A. Napier and R.P. Haslam, 2012. Metabolic engineering of the omega-3 long chain polyunsaturated fatty acid biosynthetic pathway into transgenic plants. J. Exp. Bot., 63: 2397-2410.
    CrossRefDirect Link

  94. Tang, G., J. Qin, G.G. Dolnikowski, R.M. Russel and M.A. Grusak, 2009. Golden rice is an effective source of vitamin A. Am. J. Clin. Nutr., 89: 1776-1783.
    CrossRefDirect Link

  95. Tang, G., Y. Hu, S.A. Yin, Y. Wang, G.E. Dallal, M.A. Grusak and R.M. Russell, 2012. Retracted: β-carotene in golden rice is as good as β-carotene in oil at providing vitamin A to children. Am. J. Clin. Nutr., 96: 658-664.
    CrossRefDirect Link

  96. Ye, X., S. Al-Babili, A. Klöti, J. Zhang, P. Lucca, P. Beyer and I. Potrykus, 2000. Engineering the provitamin A (β-Carotene) biosynthetic pathway into (Carotenoid-free) rice endosperm. Science, 287: 303-305.
    CrossRefDirect Link

  97. Diretto, G., S. Al-Babili, R. Tavazza, V. Papacchioli, P. Beyer and G. Giuliano, 2007. Metabolic engineering of potato carotenoid content through tuber-specific over expression of a bacterial mini-pathway. PLoS ONE, Vol. 2.
    CrossRefDirect Link

  98. Goo, Y.M., T.W. Kim, M.K. Lee and S.W. Lee, 2013. Accumulation of PrLeg, a perilla legumin protein in potato tuber results in enhanced level of sulphur-containing amino acids. C. R. Biol., 336: 433-439.
    CrossRefDirect Link

  99. Bovy, A., R. de Vos, M. Kemper, E. Schijlen and M.A. Pertejo et al., 2002. High-flavonol tomatoes resulting from the heterologous expression of the maize transcription factor genes LC and C1. Plant Cell, 14: 2509-2526.
    CrossRefDirect Link

  100. Butelli, E., L. Titta, M. Giorgio, H.P. Mock and A. Matros et al., 2008. Enrichment of tomato fruit with health-promoting anthocyanins by expression of select transcription factors. Nat. Biotechnol., 26: 1301-1308.
    CrossRefDirect Link

  101. Muir, S.R., G.J. Collins, S. Robinson, S. Hughes and A. Bovy et al., 2001. Overexpression of petunia chalcone isomerase in tomato results in fruit containing increased levels of flavonols. Nat. Biotechnol., 19: 470-474.
    CrossRefDirect Link

  102. Shi, J., C. Lang, X. Wu, R. Liu and T. Zheng et al., 2015. RNAi knockdown of fatty acid elongase1 alters fatty acid composition in Brassica napus. Biochem. Biophys. Res. Commun., 466: 518-522.
    CrossRefDirect Link

  103. Beck, K., C.A. Conlon, R. Kruger, J. Coad and W. Stonehouse, 2011. Gold kiwifruit consumed with an iron-fortified breakfast cereal meal improves iron status in women with low iron stores: A 16-week randomised controlled trial. Br. J. Nutr., 105: 101-109.
    CrossRefDirect Link

  104. Vereshchagina, Y.V., V.P. Bulgakov, V.P. Grigorchuk, V.G. Rybin and G.N. Veremeichik et al., 2014. The rolC gene increases caffeoylquinic acid production in transformed artichoke cells. Appl. Microbiol. Biotechnol., 98: 7773-7780.
    CrossRefDirect Link

  105. Liu, S., Y. Hu, X. Wang, J. Zhong and Z. Lin, 2006. High content of resveratrol in lettuce transformed with a stilbene synthase gene of Parthenocissus henryana. J. Agric. Food Chem., 54: 8082-8085.
    CrossRefPubMedDirect Link

  106. Goel, M.K., S. Mehrotra and A.K. Kikreja, 2011. Elictor-induced cellular and molecular events are responsible for productivity enhancement in hairy root cultures: An insight study. Appl. Biochem. Biotechnol., 165: 1342-1355.
    CrossRefDirect Link

  107. Qiao, J.J., Y.J. Yuan, H. Zhao, J.C. Wu and A.P. Zeng, 2003. Apoptotic cell death in suspension cultures of Taxus cuspidate co-treated with salicylic acid and hydrogen peroxide. Biotechnol. Lett., 25: 387-390.
    CrossRefDirect Link

  108. Mishra, A.K., K. Sharma and R.S. Misra, 2012. Elicitor recognition, signal transduction and induced resistance in plants. J. Plant Interact., 7: 95-120.
    CrossRefDirect Link

  109. Naik, P.M. and J.M. Al-Khayri, 2016. Impact of abiotic elicitors on in vitro production of plant secondary metabolites: A review. J. Adv. Res. Biotechnol., Vol. 1.
    CrossRefDirect Link

  110. Yang, L., K.S. Wen, X. Ruan, Y.X. Zhao, F. Wei and Q. Wang, 2018. Response of plant secondary metabolites to environmental factors. Molecules, Vol. 23.
    CrossRefDirect Link

  111. Jeong, G.T. and D.H. Park, 2006. Enhanced Secondary Metabolite Biosynthesis by Elicitation in Transformed Plant Root System. In: Twenty-Seventh Symposium on Biotechnology for Fuels and Chemicals, McMillan, J.D., W.S. Adney, J.R. Mielenz and K.T. Klasson (Eds.), Humana Press, United States, ISBN: 978-1-59745-268-7, pp: 436-446.
    CrossRefDirect Link

  112. Parida, A.K. and A.B. Das, 2005. Salt tolerance and salinity effects on plants: A review. Ecotoxicol. Environ. Saf., 60: 324-349.
    CrossRefPubMedDirect Link

  113. Navarro, J.M., P. Flores, C. Garrido and V. Martinez, 2006. Changes in the contents of antioxidant compounds in pepper fruits at different ripening stages, as affected by salinity. Food Chem., 96: 66-73.
    CrossRefDirect Link

  114. Hussein, E.A. and E.M. Aqlan, 2011. Effect of mannitol and sodium chloride on some total secondary metabolites of fenugreek calli cultured in vitro. Plant Tissue Cult. Biotechnol., 21: 35-43.
    CrossRefDirect Link

  115. Abhilash, J.E., V.V. Radhakrishnan and K.V. Mohanan, 2016. Variation in total polyamine content in some native rice cultivars of North Kerala, India in response to salinity stress. Int. J. Agric. Environ. Biotechnol., 9: 731-738.
    CrossRefDirect Link

  116. Liu, C.Z., C. Guo, Y.C. Wang and F. Ouyang, 2002. Effect of light irradiation on hairy root growth and artemisinin biosynthesis of Artemisia annua L. Process Biochem., 38: 581-585.
    CrossRefDirect Link

  117. Hemm, M.R., S.D. Rider, J. Ogas, D.J. Murry and C. Chapple, 2004. Light induces phenylpropanoid metabolism in Arabidopsis roots. Plant J., 38: 765-778.
    CrossRefPubMedDirect Link

  118. Jaakola, L. and A. Hohtola, 2010. Effect of latitude on flavonoid biosynthesis in plants. Plant Cell Environ., 33: 1239-1247.
    CrossRefDirect Link

  119. Dębski, H., W. Wiczkowski, D. Szawara-Nowak, N. Bączek, M. Szwed and M. Horbowicz, 2017. Enhanced light intensity increases flavonol and anthocyanin concentrations but reduces flavone levels in the cotyledons of common buckwheat seedlings. Cereal Res. Commun., 45: 225-233.
    CrossRefDirect Link

  120. Ferrari, S., 2010. Biological Elicitors of Plant Secondary Metabolites: Mode of Action and Use in the Production of Nutraceutics. In: Bio-Farms for Nutraceuticals: Functional Food and Safety Control by Biosensors, Giardi, M.T., G. Rea and B. Berra (Eds.), Springer, Boston, United States, ISBN: 978-1-4419-7347-4, pp: 152-166.
    CrossRefDirect Link

  121. Gai, Q.Y., J. Jiao, M. Luo, W. Wang, C.J. Zhao, Y.J. Fu and W. Ma, 2016. UV elicitation for promoting astragaloside production in Astragalus membranaceus hairy root cultures with transcriptional expression of biosynthetic genes. Ind. Crops Prod., 84: 350-357.
    CrossRefDirect Link

  122. Yu, K.W., H.N. Murthy, E.J. Hahn and K.Y. Paek, 2005. Ginsenoside production by hairy root cultures of Panax ginseng: Influence of temperature and light quality. Biochem. Eng. J., 23: 53-56.
    CrossRefDirect Link

  123. Mewis, I., I.M. Smetanska, C.T. Müller and C. Ulrichs, 2011. Specific poly-phenolic compounds in cell culture of Vitis vinifera L. cv. gamay fréaux. Appl. Biochem. Biotechnol., 164: 148-161.
    CrossRefDirect Link

  124. Uppalapati, S.R., P. Ayoubi, H. Weng, D.A. Palmer, R.E. Mitchell, W. Jones and C.L. Bender, 2005. The phytotoxin coronatine and methyl jasmonate impact multiple phytohormone pathways in tomato. Plant J., 42: 201-217.
    CrossRefDirect Link

  125. Wasternack, C. and B. Hause, 2013. Jasmonates: Biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany. Ann. Bot., 111: 1021-1058.
    CrossRefDirect Link

  126. Ali, M.B., K.W. Yu, E.J. Hahn and K.Y. Paek, 2006. Methyl jasmonate and salicylic acid elicitation induces ginsenosides accumulation, enzymatic and non-enzymatic antioxidant in suspension culture Panax ginseng roots in bioreactors. Plant Cell Rep., 25: 613-620.
    CrossRefDirect Link

  127. Shabani, L., A.A. Ehsanpour, G. Asghari and J. Emami, 2009. Glycyrrhizin production by in vitro cultured Glycyrrhiza glabra elicited by methyl jasmonate and salicylic acid. Russ. J. Plant Physiol., 56: 621-626.
    CrossRefDirect Link

  128. Xu, Y.W., S.S. Lv, D. Zhao, J.W. Chen, W.T. Yang and W. Wu, 2012. Effects of salicylic acid on monoterpene production and antioxidant systems in Houttuynia cordata. Afr. J. Biotechnol., 11: 1364-1372.
    CrossRefDirect Link

  129. Saw, N.M.M.T., H. Riedel, O. Kutuk, K. Ravichandran and I. Smetanska, 2010. Effect of elicitors and precursors on the synthesis of anthocyanin in grape Vitis vinifera cell cultures. Energy Res. J., 1: 189-192.
    CrossRefDirect Link

  130. Sharma, A., V. Kumar, P. Giridhar and G.A. Ravishankar, 2008. Induction of in vitro flowering in Capsicum frutescens under the influence of silver nitrate and cobalt chloride and pollen transformation. Electron. J. Biotechnol., 11: 84-89.
    CrossRefDirect Link

  131. El-Bahr, M.K., S.A.E.H. Bekheet, A.M.M. Gabr, R. El-Shenawy and Y.S. El Abd, 2018. Accumulation of cynarin, the hepatoprotective compound, in ethephon treated callus cultures of globe artichoke (Cynara scolymus L.). J. Biol. Sci., 18: 243-250.
    CrossRefDirect Link

  132. Sinilal, B., R. Ovadia, A. Nissim-Levi, A. Perl, M. Carmeli-Weissberg and M. Oren-Shamir, 2011. Increased accumulation and decreased catabolism of anthocyanins in red grape cell suspension culture following magnesium treatment. Planta, 234: 61-71.
    CrossRefDirect Link

  133. Hernandez, X.E., A.A. Orden, O.S. Giordano and M. Kurina, 2005. Effects of elicitor and copper sulfate on grindelic acid production in submerged cultures of Grindelia pulchella. Electron. J. Biotechnol., 8: 276-283.
    Direct Link

  134. Vasconsuelo, A. and R. Boland, 2007. Molecular aspects of the early stages of elicitation of secondary metabolites in plants. Plant Sci., 172: 861-875.
    CrossRefDirect Link

  135. Yu, L.J., W.Z. Lan, W.M. Qin, W.W. Jin and H.B. Xu, 2002. Oxidative stress and taxol production induced by fungal elicitor in cell suspension cultures of Taxus chinensis. Biol. Plant., 45: 459-461.
    CrossRefDirect Link

  136. Putalun, W., W. Luealon, W. De-Eknamkul, H. Tanaka and Y. Shoyama, 2007. Improvement of artemisinin production by chitosan in hairy root cultures of Artemisia annua L. Biotechnol. Lett., 29: 1143-1146.
    CrossRefDirect Link

  137. Kim, H.J., F. Chen, X. Wang and N.C. Rajapakse, 2005. Effect of chitosan on the biological properties of sweet basil (Ocimum basilicum L.). J. Agric. Food Chem., 53: 3696-3701.
    CrossRefPubMedDirect Link

  138. Orlita, A., M. Sidwa‐Gorycka, M. Paszkiewicz, E. Malinski and J. Kumirska et al., 2008. Application of chitin and chitosan as elicitors of coumarins and furoquinolone alkaloids in Ruta graveolens L. (common rue). Biotechnol. Appl. Biochem., 51: 91-96.
    CrossRefDirect Link

  139. Purwianingsih, W., R.Y. Hidayat and A. Rahmat, 2019. Increasing anthraquinone compounds on callus leaf Morinda citrifolia (L.) by elicitation method using chitosan shell of shrimps (Penaeus monodon). J. Phys. Conf. Ser., Vol. 1280.
    CrossRefDirect Link

  140. Taurino, M., I. Ingrosso, L. D’amico, S. de Domenico and I. Nicoletti et al., 2015. Jasmonates elicit different sets of stilbenes in Vitis vinifera cv. Negramaro cell cultures. SpringerPlus, Vol. 4.
    CrossRefDirect Link

  141. Taha, H.S. and H.M.A. El-Ghit, 2018. Implement of biotic and abiotic stress for enhancement and production of capsaicin in suspension cultures of Capsicum annuam spp. Pak. J. Biol. Sci., 21: 292-299.
    CrossRefDirect Link

  142. Cai, S., O. Wang, W. Wu, S. Zhu and F. Zhou et al., 2012. Comparative study of the effects of solid-state fermentation with three filamentous fungi on the total phenolics content (TPC), flavonoids, and antioxidant activities of subfractions from oats (Avena sativa L.). J. Agric. Food Chem., 60: 507-513.
    CrossRefDirect Link

  143. Saxena, P., S. Ahlawat, A. Ali, S. Khan and M.Z. Abdin, 2017. Gene expression analysis of the withanolide biosynthetic pathway in hairy root cultures of Withania somnifera elicited with methyl jasmonate and the fungus Piriformospora indica. Symbiosis, 71: 143-154.
    CrossRefDirect Link

  144. Zhang, B., L.P. Zheng, W.Y. Li and J.W. Wang, 2013. Stimulation of artemisinin production in Artemisia annua hairy roots by Ag-SiO2 core-shell nanoparticles. Curr. Nanosci., 9: 363-370.
    CrossRefDirect Link

  145. Ghasemi, B., R. Hosseini and F.D. Nayeri, 2015. Effects of cobalt nanoparticles on artemisinin production and gene expression in Artemisia annua. Turk. J. Bot., 39: 769-777.
    CrossRefDirect Link

  146. Shakeran, Z., M. Keyhanfar, G. Asghari and M. Ghanadian, 2015. Improvement of atropine production by different biotic and abiotic elicitors in hairy root cultures of Datura metel. Turk. J. Biol., 39: 111-118.
    CrossRefDirect Link

  147. Jamshidi, M., F. Ghanati, A. Rezaei and E. Bemani, 2016. Change of antioxidant enzymes activity of hazel (Corylus avellana L.) cells by AgNPs. Cytotechnology, 68: 525-530.
    CrossRefDirect Link

  148. Moharrami, F., B. Hosseini, A. Sharafi and M. Farjaminezhad, 2017. Enhanced production of hyoscyamine and scopolamine from genetically transformed root culture of Hyoscyamus reticulatus L. elicited by iron oxide nanoparticles. In vitro Cell. Dev. Biol. Plant, 53: 104-111.
    CrossRefDirect Link

  149. Javed, R., A. Mohamed, B. Yücesan, E. Gürel, R. Kausar and M. Zia, 2017. CuO nanoparticles significantly influence in vitro culture, steviol glycosides, and antioxidant activities of Stevia rebaudiana Bertoni. Plant Cell Tissue Organ Cult., 131: 611-620.
    CrossRefDirect Link

  150. Javed, S.B., A.A. Alatar, R. Basahi, M. Anis, M. Faisal and F.M. Husain, 2017. Copper induced suppression of systemic microbial contamination in Erythrina variegata L. during in vitro culture. Plant Cell Tissue Organ Cult., 128: 249-258.
    CrossRefDirect Link

  151. Kim, D.H., J. Gopal and I. Sivanesan, 2017. Nanomaterials in plant tissue culture: The disclosed and undisclosed. RSC Adv., 7: 36492-36505.
    CrossRefDirect Link

  152. Marslin, G., C.J. Sheeba and G. Franklin, 2017. Nanoparticles alter secondary metabolism in plants via ROS burst. Front. Plant Sci., Vol. 8.
    CrossRefDirect Link

  153. Chung, I.M., G. Rajakumar and M. Thiruvengadam, 2018. Effect of silver nanoparticles on phenolic compounds production and biological activities in hairy root cultures of Cucumis anguria. Acta Biol. Hung., 69: 97-109.
    CrossRefDirect Link

  154. Chung, I.M., K. Rekha, G. Rajakumar and M. Thiruvengadam, 2018. Production of bioactive compounds and gene expression alterations in hairy root cultures of Chinese cabbage elicited by copper oxide nanoparticles. Plant Cell Tissue Organ Cult., 134: 95-106.
    CrossRefDirect Link

  155. Bhat, P. and A. Bhat, 2016. Silver nanoparticles for enhancement of accumulation of capsaicin in suspension culture of Capsicum sp. J. Exp. Sci., 7: 1-6.
    CrossRefDirect Link

  156. Georgiev, M.I., J. Weber and A. Maciuk, 2009. Bioprocessing of plant cell cultures for mass production of targeted compounds. Appl. Microbiol. Biotechnol., 83: 809-823.
    CrossRefDirect Link

  157. Georgiev, M.I., R. Eibl and J.J. Zhong, 2013. Hosting the plant cells in vitro: Recent trends in bioreactors. Appl. Microbiol. Biotechnol., 97: 3787-3800.
    CrossRefDirect Link

  158. Huang, T.K. and K.A. McDonald, 2012. Bioreactor systems for in vitro production of foreign proteins using plant cell cultures. Biotechnol. Adv., 30: 398-409.
    CrossRefDirect Link

  159. Garcia-Ochoa, F. and E. Gomez, 2009. Bioreactor scale-up and oxygen transfer rate in microbial processes: An overview. Biotechnol. Adv., 27: 153-176.
    CrossRefPubMedDirect Link

  160. Wu, C.H., H.N. Murthy, E.J. Hahn and K.Y. Paek, 2007. Large-scale cultivation of adventitious roots of Echinacea purpurea in airlift bioreactors for the production of chichoric acid, chlorogenic acid and caftaric acid. Biotechnol. Lett., 29: 1179-1182.
    CrossRefDirect Link

  161. Kusakari, K., M. Yokoyama, S. Inomata, Y. Gozu, C. Katagiri and Y. Sugimoto, 2012. Large-scale production of saikosaponins through root culturing of Bupleurum falcatum L. using modified airlift reactors. J. Biosci. Bioeng., 113: 99-105.
    CrossRefDirect Link

  162. Sivakumar, G., K.W. Yu and K.Y. Paek, 2005. Production of biomass and ginsenosides from adventitious roots of Panax ginseng in bioreactor cultures. Eng. Life Sci., 5: 333-342.
    CrossRefDirect Link

  163. Szopa, A., A. Kokotkiewicz, M. Bednarz, K. Jafernik, M. Luczkiewicz and H. Ekiert, 2019. Bioreactor type affects the accumulation of phenolic acids and flavonoids in microshoot cultures of Schisandra chinensis (Turcz.) Baill. Plant Cell Tissue Organ Cult., 139: 199-206.
    CrossRefDirect Link

  164. Vives, K., I. Andújar, J.C. Lorenzo, O. Concepción, M. Hernández and M. Escalona, 2017. Comparison of different in vitro micropropagation methods of Stevia rebaudiana B. including temporary immersion bioreactor (BIT®). Plant Cell Tissue Organ Cult., 131: 195-199.
    CrossRefDirect Link

Keywords


  • bioreactors
  • Nutraceuticals
  • in vitro culture
  • mutation
  • transformation
  • hairy roots
  • elicitation

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