Mulberroside A Accumulation in Mulberry Plantlets from In Vitro Culture and Hydroponic System
Main Article Content
Abstract
In this study, nodal explants cultured in MS medium supplemented with BAP 4mg/l and NAA 0.5 mg/l induced 3.33 shoots per explant within 4 weeks. The elongated multiple shoots were transferred to rooting media. The best root development was found on MS medium without PGRs within 10 days. The acclimatized plants were transferred to a deep-water hydroponic system with different concentrations of MS nutrient solution without sucrose addition. The results showed that mulberry plants cultivated in 1/8 MS nutrient solution gave the highest growth index. For mulberroside A determination, the results showed that mulberroside A accumulation in roots were higher than in shoots of mulberry plants both for in vitro culture and in the hydroponic system. In the case of in vitro culture, mulberroside A accumulation in roots was 20.61 mg/g DW, and in shoots was 11.98 mg/g DW. In hydroponic system, mulberroside A accumulation in roots was 17.58 mg/g DW, and in shoots was 2.34 mg/g DW. We also found that the higher concentration of MS nutrient solution, the more mulberroside A accumulation in roots of mulberry plants cultivated in the hydroponic system.
Keywords: plant tissue culture; root induction; secondary metabolites; shoot multiplication; soilless culture
*Corresponding author: E-mail: pana.lo@kmitl.ac.th
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References
Rohela, G.K., Shukla, P., Muttanna, Kumar, R. and Chowdhury, S.R., 2020. Mulberry (Morus spp.): An ideal plant for sustainable development. Trees, Forests and People, 2, DOI: 10.1016/j.tfp.2020.100011.
Inyai, C., Udomsin, O., Komaikul, J., Tanaka, H., Sritularak, B. and Putalun, W., 2015. Enhancement mulberroside A production in Morus alba L. cell cultures by calcium alginate immobilization and elicitation. Isan Journal of Pharmaceutical Sciences, 10(suppl.), 27-32.
Singhal, B.K., Khan, M.A., Dhar, A., Baqual, F.M., Bindroo, B.B., 2010. Approaches to industrial exploitation of mulberry (Mulberry sp.) fruits. Journal of Fruit and Ornamental Plant Research, 18, 83-99.
Wen, P., Hu, T., Linhardt, R.J., Liao, S., Wu, H. and Zou Y., 2019. Mulberry: A review of bioactive compounds and advanced processing technology. Trends in Food Science and Technology, 83, 138-158.
Abbas, G.M., Bar, F.M.A., Baraka, H.N., Gohar, A.A., and Lahloub, M.F., 2014. A new antioxidant stilbene and other constituents from the stem bark of Morus nigra L. Natural Product Research, 28, 952-959.
Oh, Y. C., Kang, O.H., Choi, J.G., Chae, H.S., Lee, Y.S., Brice, O.O., Jung, H.J., Hong, S., Lee, Y. and Kwon, D., 2009. Anti- inflammatory effect of resveratrol by inhibition of IL-8 production in LPS-induced THP-1 cells. American Journal of Chinese Medicine, 37, 1203-1214.
Lee, J.H., Baek, S.Y., Jang, E.J., Ku, S.K., Kim, K.M. and Ki, S.H., 2018. Oxyresveratrol ameliorates nonalcoholic fatty liver disease by regulating hepatic li- pogenesis and fatty acid oxidation through liver kinase B1 and AMP-activated protein kinase. Chemico-biological Interactions, 289, 68-74.
Ahn, E., Lee, J., Jeon, Y.H., Choi, S.W. and Kim, E., 2017. Anti-diabetic effects of mulberry (Morus alba L.) branches and oxyresveratrol in streptozotocin-induced diabetic mice. Food Science and Biotechnology, 26, 1693-1702.
Chen, Y.C., Tien, Y.J., Chen, C.H., Beltran, F.N., Amor, E.C., Wang, R.J., Wu, D., Mettling, C., Lin, Y. and Yang W., 2013. Morus alba and active compound oxyresveratrol exert anti-inflammatory activity via inhibition of leukocyte migration involving MEK/ERK signaling. BMC Complementary and Alternative Medicine, 13, 45-54.
Sharma, R., Sharma, A., Shono, T., Takasugi, M., Shirata, A., Fujimura, T. and Machii, H., 2001. Mulberry moracins: Scavengers of UV stress-generated free radicals. Bioscience Biotechnology and Biochemistry, 65, 1402-1405.
Seong, S.H., Ha, M.T., Min, B.S., Jung, H.A. and Choi, J.S., 2018. Moracin derivatives from Morus Radix as dual BACE1 and cholinesterase inhibitors with antioxidant and anti-glycation capacities. Life Sciences, 210, 20-28.
Park, K.M., You, J.S., Lee, H.Y., Baek, N.T. and Hwang, J.K., 2003. Kuwanon G: An antibacterial agent from the root bark of Morus alba against oral pathogens. Journal of Ethnopharmacology, 84, 181-185.
Simonetti, G., Brasili, E., D'Auria, F.D., Corpolongo, S., Ferrari, F., Pasqua, G. and Valletta, A., 2017. Prenylated flavonoids and total extracts from Morus nigra L. root bark inhibits in vitro growth of plant pathogenic fungi. Plant Biosystems, 151, 783-787.
Chen, Z., Du, X., Yang, Y., Cui, X., Zhang, Z. and Li, Y., 2018. Comparative study of chemical composition and active components against α-glucosidase of various medicinal parts of Morus alba L. Biomedical Chromatography, 32(11), 4328-4337.
Paudel, P., Yu, T., Seong, S.H., Kuk, E.B., Jung, H.A. and Choi, J.S., 2018. Protein tyrosine phosphatase 1B inhibition and glucose uptake potentials of mulberrofuran G, albanol B, and kuwanon G from root bark of Morus alba L. in insulin-resistant HepG2 cells: An in vitro and in silico study. International Journal of Molecular Sciences, 19, 1542-1560.
Lorenz, P., Roychowdhury, S., Engelmann, M., Wolf, G., and Horn, T.F.W., 2003. Oxyresveratrol and resveratrol are potent antioxidants and free radical scavengers: effect on nitrosative and oxidative stress derived from microglial cells. Nitric Oxide, 9, 64-76.
Kim, J., Kim, M., Sho, S., Kim, M., Kim, S. and Lim, Y., 2010. Biotransformation of mulberroside A from Morus alba results in enhancement of tyrosinase inhibition. The Journal of Industrial Microbiology and Biotechnology, 37, 631-637.
Jo, S.P., Kim, J.K. and Lim, Y.H., 2014. Antihyperlipidemic effects of stilbenoids isolated from Morus alba in rats fed a high-cholesterol diet. Food and Chemical Toxicology, 65, 213-218.
Kiferle, C., Maggini. R. and Pardossi. A., 2013. Influence of nitrogen nutrition on growth and accumulation of rosmarinic acid in sweet basil (Ocimum basilicum L.) grown in hydroponic culture. Australian Journal of Crop Science, 7, 321-327.
Gontier, E., Clement, A., Tran, T.L.M., Grevot, A., Lievre, K., Guckert, A. and Bourgaub, F., 2002. Hydroponic combined with natural or forced root permeabilization: a promising technique for plant secondary metabolite production. Plant Science, 163, 723-732.
Rattan, S., Partap, M., Kanika., Kumar, S. and Warghat, A.R., 2022. Nutrient feeding approach enhances the vegetative growth biomass, volatile oil composition, and myristicin content in hydroponically cultivated Petroselinum crispum (Mill.) Nyman. Journal of Applied Research on Medicinal and Aromatic Plants, 26, DOI: 10.1016/j.jarmap.2021.100359.
Vu, T.D., Jousse, C., Pawlicki-jullian, N., Schiltz, S., Nguyen, T.K.O., Tran, T.L.M., Bouquet, L., Hehn, A., Boitel-conti, M., Moussaron, J., Biteau, F., Assaf-ducrocq, C., Robin, C., Bourgaud, F., Guckert, A. and Gontier, E., 2018. Datura innoxia plants hydroponically-inoculated with Agrobacterium rhizogenes display an enhanced growth and alkaloid metabolism. Plant Science, 227, 166-176.
Bafort, F., Kohnen, S., Maron, E., Bouhadada, A., Ancion, A., Crutzen, N. and Jijakli, M.H., 2022. The agro-economic feasibility of growing the medicinal plant Euphorbia peplus in a modified vertical hydroponic shipping container. Horticulturae, 8(3), DOI: 10.3390/horticulturae8030256.
Greathouse, J., Henning, S. and Soendergaard, M., 2021. Effect of grafting rootstock on the antioxidant capacity and content of heirloom tomatoes (Solanum lycopersicum L.) in hydroponic culture. Plants, 10(5), DOI: 10.3390/plants10050965.
Murashige, T. and Skoog, F., 1962. A revised medium for rapid growth and bio assays with tobacco tissue cultures. Plant Physiology, 15, 473-497.
Zhou, J., Li, S.-X., Wang, W., Guo, X.-Y., Lu, X.-Y., Yan, X.-P., Huang, D., Wei, B.-Y. and Cao, L., 2013. Variations in the levels of mulberroside A, oxyresveratrol, and resveratrol in mulberries in different seasons and during growth. The Scientific World Journal, 2013, DOI: 10.1155/2013/380692.
Sajeevan, R.S., Singh, S.J., Nataraja, K.N. and Shivanna, M.B., 2011. An efficient in vitro protocol for multiple shoot induction in mulberry, Morus alba L variety V1. International Research Journal of Plant Science, 2, 254-261.
Aroonpong, P. and Chang, J., 2015. Micropropagation of a difficult-to-root weeping mulberry (Morus alba ver. Shidareguwa): A popular variety for ornamental purposes. Scientia Horticulturae, 194, 320-326.
Vijayan, K., Chakraborti, S.P. and Roy, B.N., 1998. Regeneration of plantlets through callus culture in mulberry. Indian Journal of Plant Physiology, 3(4), 310-313.
Hussain, S.A., Anis, M. and Alatar, A.A., 2020. Efficient in vitro regeneration system for Tecoma stans L., using shoot tip and assessment of genetic fidelity among regenerants. Proceedings of the National Academy of Sciences, India Section B: Biological Sciences, 90, 171-178.
Podwyszynska, M. 2003. Cell, tissue and organ culture. rooting of micropropagated shoot. Encycopedia of Rose Science, 2003, 66-76.
Ludwig-Muller, J., Vertocnik, A. and Town, C.D., 2005. Analysis of indole-3-butyric acid-induced adventitious root formation on Arabidopsis stem segments. Journal of Experimental Botany, 56, 2095-2105.