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Physiological responses of the leaves of a high-altitude plant Picrorhiza kurroa to cold stress

Authors

DOI:

https://doi.org/10.14719/pst.2861

Keywords:

antioxidant, pigments, lipid peroxidation, osmoprotectants, cold stress, Picrorhiza kurroa

Abstract

Plants growing at high elevations experience different environmental stresses, such as drought, salt, and cold. Among them, cold stress is the most prevalent one that affects the plants differently. Plants undergo biochemical, metabolic, molecular, and physiological changes under cold stress; hence, they adopt various mechanisms to tolerate it. The antioxidant defence system, osmotic regulators, and photosynthetic pigments in the plant provide them with stress tolerance. The present study is conducted on a high-altitude plant, Picrorhiza kurroa, which grows in such environmental conditions, to study the physiological parameters that provide a coping mechanism against cold stress. For this study, the leaves were collected from Pothivasa (2200 m.a.s.l) and Tungnath (3600 m.a.s.l) in Rudraprayag, Uttarakhand, India. The photosynthetic pigments (chlorophyll a, chlorophyll b, and carotenoids), lipid peroxidation, antioxidant enzymes, namely, superoxide dismutase, catalase, guaiacol peroxidase, ascorbate peroxidase, glutathione reductase, and osmoprotectants (protein, soluble sugar, and proline) present in the leaves were determined to visualize the impact of cold stress. It was revealed that the concentration of photosynthetic pigments increased with elevation. The activity of enzymes was analyzed, and they were observed to decrease with altitude. The malondialdehyde concentration, an indicator of lipid peroxidation, is higher in Pothivasa and lower in Tungnath. There is a significant increase in the osmoprotectants’ content along the altitudinal gradient. Therefore, the leaves from both sampling locations revealed the physiological changes that occurred in them to adapt to the cold stress conditions.

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References

Lichtenthaler HK. The stress concept in plants: An introduction. Ann NY Acad Sci. 2006;851:187-98. https://doi.org/10.1111/j.1749-6632.1998.tb08993.x

Mboup M, Fischer I, Lainer H, Stephan W. Trans-species polymorphism and allele-specific expression in the cbf gene family of wild tomatoes. MolBiolEvol. 2012;29:3641-52. https://doi.org/10.1093/molbev/mss176

Ritonga FN, Chen S. Physiological and molecular mechanism involved in cold stress tolerance in plants. Plants. 2020;9:560.https://doi.org/10.3390/plants9050560

Zhang F, Jiang Y, Bai LP, Zhang L, Chen LJ, Li HG, Yin Y, Yan WW, Yi Y, Guo ZF. The ICE-CBF-COR pathway in cold acclimation and AFPs in plants. Middle-East JSci Res. 2011;8:493-98.

Sun X, Zhu Z, Zhang L, Fang L, Zhang J, Wang Q, Li S, Liang Z, Xin H. Overexpression of ethylene response factors VaERF080 and VaERF087 from Vitisamurensis enhances cold tolerance in Arabidopsis. SciHortic. 2019;243:320-26. https://doi.org/10.1016/j.scienta.2018.08.055

Demidchik V, Straltsova D, Medvedev SS, Pozhvanov GA, Sokolik A, Yurin V. Stress-induced electrolyte leakage: The role of K+-permeable channels and involvement in programmed cell death and metabolic adjustment. JExp Bot. 2014;65:1259-70. https://doi.org/10.1093/jxb/eru004

Tolosa LN, Zhang Z. The role of major transcription factors in solanaceousfood crops under different stress conditions: Current and future perspectives. Plants. 2020;9:56. https://doi.org/10.3390/plants9010056

Chen L, Zhao Y, Xu S, Zhang Z, Xu Y, Zhang J, Chong K. OsMADS57 together with OsTB 1 coordinates transcription of its target OsWRKY94 and D14 to switch its organogenesis to defense for cold adaptation in rice. New Phytol. 2018;218:219-31. https://doi.org/10.1111/nph.14977

Cuimei Z, Shangli S, Zhen L, Fan Y, Guoli Y. Drought tolerance in alfalfa (Medicago sativa L.) varieties is associated with enhanced antioxidative protection and declined lipid peroxidation. Journal of Plant Physiology. 2019;232:226-40. https://doi.org/10.1016/j.jplph.2018.10.023

Zulfiqar F, Akram NA, Ashraf M. Osmoprotection in plants under abiotic stresses: New insights into a classical phenomenon. Planta. 2020;251:3. https://doi.org/10.1007/s00425-019-03293-1

Slama I, Abdelly C, Bouchereau A, Flowers T, Savoure A. Diversity, distribution and roles of osmoprotective compounds accumulated in halophytes under abiotic stress. Ann Bot. 2015;115:433-47. https://doi.org/10.1093/aob/mcu239

Kok D, Bahar E. Effects of different vineyard altitudes and grapevine directions on some leaf characteristics of cv. GamayVitis vinifera L. Bulg J Agric Sci. 2015;21:320-24.

Bhattacharjee S, Bhattacharya S, Jana S, Baghel DS. A review on medicinally important species of Picrorhiza. Int JPharmaceut Res Bio Sci. 2013;2(4):1-16.

Bhandari P, Kumar N, Singh B, Gupta AP, Kaul VK, Ahuja PS. Stability-indicating LC–PDA method for determination of picrosides in hepatoprotective Indian herbal preparations of Picrorhiza kurroa. Chromatographia. 2009;69(3):221-27.https://doi.org/10.1365/s10337-008-0889-7

Sah JN, Varshney VK. Chemical constituents of Picrorhiza genus: A review. Am JEssent Oils Nat Prod. 2013;1(2):22-37.

Krupashree K, Kumar KH, Rachitha P, Jayashree GV, Khanum F. Chemical composition, antioxidant and macromolecule damage protective effects of PicrorhizakurroaRoyle ex Benth. SAfr J Bot. 2014;94:249-54. https://doi.org/10.1016/j.sajb.2014.07.001

Debnath P, Rathore S, Walia S, Kumar M, Devi R, Kumar R. Picrorhiza kurroa: A promising traditional therapeutic herb from higher altitude of western Himalayas. Journal of Herbal Medicine. 2020. https://doi.org/10.1016/j.hermed.2020.100358

Lichtenthaler HK, Wellburn A. Determination of total carotenoids and chlorophylls a and b in leaf in extracts in different solvents. BiochemSoc Trans. 1982;603:591-92.https://doi.org/10.1042/bst0110591

Mukherjee SP, Choudhuri MA. Implications of water stress-induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in Vigna seedlings. Physiol Plant. 1983;58:166-70. https://doi.org/10.1111/j.1399-3054.1983.tb04162.x

Kono Y. Generation of superoxide radical during autoxidation of hydroxylamine and an assay for superoxide dismutase. Archives of Biochemistry and Biophysics. 1978;186(1):189-95. https://doi.org/10.1016/0003-9861(78)90479-4

Aebi H. Catalase in vitro. Methods Enzymol. 1984;105:121-26. https://doi.org/10.1016/S0076-6879(84)05016-3

Pütter J. Peroxidases. In Methods of Enzymatic Analysis. Academic Press. 1974;685-90. https://doi.org/10.1016/B978-0-12-091302-2.50033-5

Nakano Y, Asada K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology. 1981;22(5):867-80.

Carlberg INCER, Mannervik BENGT. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. Journal of Biological Chemistry. 1975;250(14):5475-80. https://doi.org/10.1016/S0021-9258(19)41206-4

Hedge JE, Hofreiter BT. Estimation of carbohydrate. Methods in Carbohydrate Chemistry. Academic Press, New York. 1962;17-22.

Bates LS, Waldren RP, Teare ID. Rapid determination of free proline for water-stress studies. Plant Soil. Berlin, Heidelberg, New York. 1973;39:205-07. https://doi.org/10.1007/BF00018060

Kosugi H, Kikugawa K. Thiobarbituric acid reaction of aldehydes and oxidized lipids in glacial acetic acid. Lipids. 1985;20(12);915-21. https://doi.org/10.1007/BF02534777

Bartels D, Sunkar R. Drought and salt tolerance in plants. Crit Rev Plant Sci. 2005;24(1):23-58.https://doi.org/10.1080/07352680590910410

Chen Y, Zhang X, Guo Q, Cao L, Qin Q, Li C, Zhao M, Wang W. Plant morphology, physiological characteristics, accumulation of secondary metabolites and antioxidant activities of Prunella vulgaris L. under UV solar exclusion. Biological Research. 2019;52. https://doi.org/10.1186/s40659-019-0225-8

Qin JH, Liu Q. Impact of seasonally frozen soil on germinability and antioxidant enzyme activity of Piceaasperata seeds. Can J For Res. 2009;39(4):723-30. https://doi.org/10.1139/X09-001

Cui GX, Wei XH, Degen AA, Wei XX, Zhou JW, Ding LM. Trolox-equivalent antioxidant capacity and composition of five alpine plant species growing at different elevations on the Qinghai-Tibetan Plateau. Plant Ecology & Diversity. 2016;9(4):387-96. https://doi.org/10.1080/17550874.2016.1261952

Mangral ZA, Islam SU, Tariq L, Kaur S, Ahmad R, Malik AH, Goel S, Baishya R, Barik SK, Dar TU. Altitudinal gradient drives significant changes in soil physico-chemical and eco-physiological properties of Rhododendron anthopogon: A case study from Himalaya. Frontiers in Forests and Global Change. 2023 Apr 28;6:1181299. https://doi.org/10.3389/ffgc.2023.1181299

Koh SC, Demmig-Adams B, Adams III WW. Novel patterns of seasonal photosynthetic acclimation, including interspecific differences, in conifers over an altitudinal gradient. Arctic, Antarctic and Alpine Research. 2009 Aug 1;41(3):317-22. https://doi.org/10.1657/1938.4246-41.3.317

Hashim AM, Alharbi BM, Abdulmajeed AM, Elkelish A, Hozzein WN, Hassan HM. Oxidative stress responses of some endemic plants to high altitudes by intensifying antioxidants and secondary metabolites content. Plants. 2020 Jul 9;9(7):869. https://doi.org/10.3390/plants9070869

Adams WW III, Demmig-Adams B, Rosenstiel TN, Brightwell AK, Ebbert V. Photosynthesis and photoprotection in overwintering plants. Plant Biology. 2002;4:545-57. https://doi.org/10.1096/fasebj.10.2.8641556

Armstrong GA, Hearst JE. Carotenoids 2: Genetics and molecular biology of carotenoid pigment biosynthesis. FASEB J. 1996;10(2):228-37.https://doi.org/10.1096/fasebj.10.2.8641556

Demmig-Adams B, Iii WWA. Carotenoid composition in sun and shade leaves of plants with different life forms. Plant Cell & Environment. 1992;15(4):411-19. https://doi.org/10.1111/j.1365-3040.1992.tb00991.x

Havaux M, Niyogi KK. The violaxanthin cycle protects plants from photooxidative damage by more than one mechanism. ProcNatlAcadSci USA. 1999;96(15):8762-67. https://doi.org/10.1073/pnas.96.15.8762

Karagiannis E, Tanou G, Samiotaki M, Michailidis M, Diamantidis G, Minas IS. Comparative physiological and proteomic analysis reveal distinct regulation of peach skin quality traits by altitude. Frontiers in Plant Science. 2016;7:1689. https://doi.org/10.3389/fpls.2016.01689

Rana PS, Saklani P. Analyzing effect of altitudinal variation in enzymatic antioxidants of Coleus forskohlii from Uttarakhand, India. Plant Cell Biotechnology and Molecular Biology. 2019;20(9&10):442-50. https://doi.org/10.1101/662528

Wang Y, He W, Huang H, An L, Wang D, Zhang F. Antioxidative responses to different altitudes in leaves of alpine plant Polygonum viviparum in summer. Acta Physiologiae Plantarum. 2009;31(4):839-48. https://doi.org/10.1007/s11738-009-0300-9

Hasanuzzaman M, Alam M, Rahman A, Hasanuzzaman M, Nahar K, Fujita M. Exogenous proline and glycine betaine mediated upregulation of antioxidant defense and glyoxalase systems provides better protection against salt-induced oxidative stress in two rice (Oryza sativa L.) varieties. BioMed Res Int. 2014. https://doi.org/10.1155/2014/757219

Guy CL, Huber JL, Huber SC. Sucrose phosphate synthase and sucrose accumulation at low temperature. Plant Physiol. 1992;100:502-08. https://doi.org/10.1104/pp.100.1.502

Chinnusamy V, Zhu J, Zhu JK. Cold stress regulation of gene expression in plants. Trends in Plant Science. 2007 Oct 1;12(10):444-51. https://doi.org/10.1016/j.tplants.2007.07.002

Bano A, Fatima M. Salt tolerance in Zea mays (L.) following inoculation with Rhizobium and Pseudomonas. Biol Fertility Soils. 2009;45:405-13. https://doi.org/10.1007/s00374-008-0344-9

Khan H, Shah SH, Uddin N, Azhar N, Asim M, Syed S, Ullah F, Tawab F, Inayat J. Biochemical and physiological changes of different plants species in response to heat and cold stress. ARPN J Agric Biol Sci. 2015;10:213-16.

Kandler O, Hopf H. Oligo saccharides based on sucrose. In: Encyclopedia of Plant Physiology. Berlin: Springer. 1982;13A:348-82. https://doi.org/10.1007/978-3-642-68275-9_8

Mahajan S, Tuteja N. Cold, salinity and drought stresses: An overview. Arch Biochem Biophy. 2005;444:139-58. https://doi.org/10.1016/j.envexpbot.2004.03.017

Demiral T, Turkan I. Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environ Exp Bot. 2005;53(3):247-57.https://doi.org/10.1016/j.envexpbot.2004.03.017

Alexieva V, Sergiev I, Mapelli S, Karanov E. The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat. Plant, Cell & Environment. 2001;24(12):1337-44. https://doi.org/10.1046/j.1365-3040.2001.00778.x

Cui G, Li B, He W, Yin X, Liu S, Lian L, Zhang Y, Liang W, Zhang P. Physiological analysis of the effect of altitudinal gradients on Leymus secalinus on the Qinghai-Tibetan Plateau. PloS one. 2018;13(9):e0202881.https://doi.org/10.1371/journal.pone.0202881

Published

14-12-2023

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1.
Agrawal S, Saklani P. Physiological responses of the leaves of a high-altitude plant Picrorhiza kurroa to cold stress. Plant Sci. Today [Internet]. 2023 Dec. 14 [cited 2024 Nov. 21];. Available from: https://horizonepublishing.com/journals/index.php/PST/article/view/2861

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