Biopolym. Cell. 2024; 40(1):58-67.
Molecular and Cell Biotechnologies
Effect of light and temperature on the content of some biologically active substances in Deschampsia antarctica tissue culture
1Twardovska M. O., 1Konvalyuk I. I., 2Lystvan K. V., 1Kunakh V. A.
  1. Institute of Molecular Biology and Genetics, NAS of Ukraine
    150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03143
  2. Institute of Cell Biology and Genetic Engineering, NAS of Ukraine
    148, Akademika Zabolotnogo Str., Kyiv, Ukraine, 03143

Abstract

Aim. The aim of the work was to study the influence of growth conditions (darkness/light and temperature 18°/26°C) on the content of phenolic compounds and flavonoids in D. antarctica morphogenic tissue culture. Methods. In vitro tissue culture, Folin-Ciocalteu method, spectrophotometry, HPLC analysis. Results. The total content of phenolic compounds and flavonoids in D. antarctica morphogenic tissue cultures, obtained from the plants genotypes DAR12 and G/D11-1/3 was determined. It was shown that in growth calli the light intensity of 6500 lux and raised temperature of 26°C led to a decrease in the content of biologically active substances (BAS). When culturing calli of both genotypes in the darkness, regardless of the temperature, the level of phenolic compounds (2 times for DAR12 and 2.8–3.1 times for G/D11-1/3) as well as of flavonoids (2.3–2.4 times for DAR12 and 4.6–5 times for G/D11-1/3) decreased. The antioxidant and antitumor compound tricin was found, the content of which was three times higher in the initial plant DAR12 compared to the G/D11-1/3 plant. The content of tricin in the calli was lower than in the initial plants. Conclusions. It was found that the highest level of the BAS accumulation in the morphogenic tissue culture of D. antarctica was observed when it was growing in the light intensity of 6500 lux and at the temperature of 18°C. The tricin detection in the initial plants of genotypes DAR12 and G/D11-1/3, as well as in the tissue cultures provides a basis for further biochemical study of D. antarctica in vitro as a potential source of BAS, which can be used for therapeutic and prophylactic purposes.
Keywords: Deschampsia antarctica E. Desv., plant tissue culture, phenolic compounds, flavonoids, tricin

References

[1] Ramakrishna A, Ravishankar GA. Influence of abiotic stress signals on secondary metabolites in plants. Plant Signal Behav. 2011; 6(11):1720-31.
[2] Cuba-Díaz M, Rivera-Mora C, Navarrete E, Klagges M. Advances of native and non-native Antarctic species to in vitro conservation: improvement of disinfection protocols. Sci Rep. 2020; 10(1):3845.
[3] Cotelle N. Role of flavonoids in oxidative stress. Curr Top Med Chem. 2001; 1(6):569-90.
[4] Ververidis F, Trantas E, Douglas C, Vollmer G, Kretzschmar G, Panopoulos N. Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part II: Reconstruction of multienzyme pathways in plants and microbes. Biotechnol J. 2007; 2(10):1235-49.
[5] Atanasov AG, Waltenberger B, Pferschy-Wenzig EM, Linder T, Wawrosch C, Uhrin P, Temml V, Wang L, Schwaiger S, Heiss EH, Rollinger JM, Schuster D, Breuss JM, Bochkov V, Mihovilovic MD, Kopp B, Bauer R, Dirsch VM, Stuppner H. Discovery and resupply of pharmacologically active plant-derived natural products: A review. Biotechnol Adv. 2015; 33(8):1582-614.
[6] Ochoa-Villarreal M, Howat S, Hong S, Jang MO, Jin YW, Lee EK, Loake GJ. Plant cell culture strategies for the production of natural products. BMB Rep. 2016; 49(3):149-58.
[7] Kunakh VA. Biotechnology of medicinal plants. Genetic, physiological and biochemical basis.- Kyiv: "Logos," 2005.-730p.
[8] Parnikoza I, Kozeretska I, Kunakh V. Vascular plants of the Maritime Antarctic: Origin and adaptation. Am J Plant Sci. 2011; 2(3):381-95.
[9] Ozheredova IP, Parnikoza IYu, Poronnik OO, Kozeretska IA, Demidov SV, Kunakh VA. Mechanisms of antarctic vascular plant adaptation to abiotic environmental factors. Tsitol Genet. 2015; 49(2):139-45.
[10] Köhler H, Contreras RA, Pizarro M, Cortés-Antíquera R, Zúñiga GE. Antioxidant Responses Induced by UVB Radiation in Deschampsia antarctica Desv. Front Plant Sci. 2017; 8:921.
[11] Gidekel M, Weber H, Cabrera G, Gutierrez A, Osorio J, Podhajcer O, Cafferata E, Sunkel C, Mihovilovic I. Extracts of Deschampsia antarctica Desv. with antineoplastic activity. U.S. Patent 2010/0310686 A1, December 9, 2010.
[12] Malvicini M, Gutierrez-Moraga A, Rodriguez MM, Gomez-Bustillo S, Salazar L, Sunkel C, Nozal L, Salgado A, Hidalgo M, Lopez-Casas PP, Novella JL, Vaquero JJ, Alvarez-Builla J, Mora A, Gidekel M, Mazzolini G. A Tricin Derivative from Deschampsia antarctica Desv. Inhibits Colorectal Carcinoma Growth and Liver Metastasis through the Induction of a Specific Immune Response. Mol Cancer Ther. 2018; 17(5):966-76.
[13] Bråkenhielm E, Cao R, Cao Y. Suppression of angiogenesis, tumor growth, and wound healing by resveratrol, a natural compound in red wine and grapes. FASEB J. 2001; 15(10):1798-800.
[14] Twardovska M, Konvalyuk I, Lystvan K, Andreev I, Parnikoza I, Kunakh V. Phenolic and flavonoid contents in Deschampsia antarctica plants growing in nature and cultured in vitro. Pol Polar Res. 2021; 42(2):97-116.
[15] Twardovska MO, Konvalyuk II, Lystvan KV, Andreev IO, Kunakh VA. The content of phenolic compounds and flavonoids in Deschampsia antarctica tissue culture. Biotechnol Acta. 2021; 14(2):59-66.
[16] Poronnik O, Twardovska M, Kunakh V, Andreev I, Drobyk N, Navrotska D, Nuzhyna N, Konvalyuk I, Myryuta G, Ivannikov R, Parnikoza I. Development, integrative study and research prospects of Deschampsia antarctica collection. Pol Polar Res. 2023; 44(1):41-68.
[17] Gamborg OL, Eveleigh DE. Culture methods and detection of glucanases in suspension cultures of wheat and barley. Can J Biochem. 1968; 46(5):417-21.
[18] Murashige T, Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant. 1962; 15(3):473-97.
[19] Singleton VL, Rossi JA. Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. Am J Enol Vitic. 1965; 16(3):144-58.
[20] Pękal A, Pyrzynska K. Evaluation of aluminium complexation reaction for flavonoid content assay. Food Anal Methods. 2014; 7(9):1776-82.
[21] Edwards JA, Smith RI. Photosynthesis and respiration of Colobanthus quitensis and Deschampsia antarctica from the maritime Antarctic. BAS Bulletin. 1988; 81:43-63.
[22] Kunakh VA. Supernumerary or B-chromosomes in plants. origin and biological implication. Visnyk Ukr Tov Genet Sel. 2010; 8(1):99-139.
[23] Ivannikov R, Laguta I, Anishchenko V, Skorochod I, Kuzema P, Stavinskaya O, Parnikoza I, Poronnik O, Myryuta G, Kunakh V. Composition and radical scavenging activity of the extracts from Deschampsia antarctica É. Desv. plants grown in situ and in vitro. Chem J Mold. 2021; 16(1):105-14.
[24] Li M, Pu Y, Yoo CG, Ragauskas AJ. The occurrence of tricin and its derivatives in plants. Green Chem. 2016; 18(6):1439-54.
[25] Zhou JM, Ibrahim RK. Tricin. A potential multifunctional nutraceutical. Phytochem Rev. 2010; 9(3):413-24.
[26] Zhang WK, Xu JK, Zhang L, Du GH. Flavonoids from the bran of Avena sativa. CJNM. 2012; 10(2):110-14.
[27] Moheb A, Grondin M, Ibrahim RK, Roy R, Sarhan F. Winter wheat hull (husk) is a valuable source for tricin, a potential selective cytotoxic agent. Food Chem. 2013; 138(2-3):931-7.
[28] Goufo P, Ferreira LMM, Trindade H, Rosa EAS. Distribution of antioxidant compounds in the grain of the Mediterranean rice variety 'Ariete'. J Food Res. 2015; 13(1):140-50.
[29] Cai H, Hudson EA, Mann P, Verschoyle RD, Greaves P, Manson MM, Steward WP, Gescher AJ. Growth-inhibitory and cell cycle-arresting properties of the rice bran constituent tricin in human-derived breast cancer cells in vitro and in nude mice in vivo. Br J Cancer. 2004; 91(7):1364-71.
[30] Oyama T, Yasui Y, Sugie S, Koketsu M, Watanabe K, Tanaka T. Dietary tricin suppresses inflammation-related colon carcinogenesis in male Crj: CD-1 mice. Cancer Prev Res (Phila). 2009; 2(12):1031-8.
[31] Kandaswami C, Lee LT, Lee PP, Hwang JJ, Ke FC, Huang YT, Lee MT. The antitumor activities of flavonoids. In Vivo. 2005; 19(5):895-909.
[32] Pinhatti AV, de Matos Nunes J, Maurmann N, Rosa LMG, von Poser GL, Rech SB. Phenolic compounds accumulation in Hypericum ternum propagated in vitro and during plant development acclimatization. Acta Physiol Plant. 2010; 32(4):675-81.
[33] Dias MI, Sousa MJ, Alves RC, Ferreira ICFR. Exploring plant tissue culture to improve the production of phenolic compounds: A review. Ind Crop Prod. 2016; 82:9-22.