Salt and drought stress exhibits oxidative stress and modulated protein patterns in roots and leaves of date palm (Phoenix dactylifera L.)

Hussein J. SHAREEF, Jameel M. AL-KHAYRI

Abstract


The formation of new proteins under the influence of harsh environmental conditions is a plant adaptation reaction. Two-year-old date palm tissue culture-derived plants from ‘Barhee’ grown in the field were subjected to salt stress (70 g l-1 NaCl) and dehydration-induced by applying 70 g l-1 polyethylene glycol or without irrigation and withholding irrigation (0 g l-1) for one month. The soluble carbohydrate content increased in response to salinity and polyethylene glycol treatment in leaves compared to the control and drought treatment without irrigation. Proline increased in all treatments. Malondialdehyde and hydrogen peroxide increased under salinity. Salinity treatment increased the activity of ascorbate peroxidase and catalase enzyme. Salinity and polyethylene glycol treatments increased abscisic acid, whereas the indoleacetic acid level decreased. The protein pattern of roots and leaves in one-dimensional polyacrylamide gel electrophoresis showed that the stress conditions led to new protein bands' appearance and other proteins' disappearance. A comparison of protein patterns between the control and stress treatments revealed that the relative intensity of proteins in roots and leaves were more associated with salinity treatment than the drought. The results may be clearing important the molecular mechanism of tolerance under the influence of extreme environmental stress.


Keywords


abscisic acid; ascorbate peroxidase; lipid peroxidation; malondialdehyde; polypeptide

Full Text:

PDF

References


Acosta-Motos, J.R., Ortuño, M.F., & Bernal-Vicente, A. (2017). Plant responses to salt stress: adaptive mechanisms. Agronomy, (7),18. https://doi.org/10.3390/agronomy7010018

Al-Bahrany, A.M., & Al-Khayri, J.M. (2012). In vitro responses of date palm cell suspensions under osmotic stress induced by sodium, potassium, and calcium salts at different exposure durations. American Journal of Plant Physiology,7(3), 120–134. http://dx.doi.org/10.3923/ajpp.2012.120.134

Al Hassan, M., Martínez Fuertes, M., Ramos Sánchez, F. J., Vicente, O., & Boscaiu, M. (2015). Effects of salt and water stress on plant growth and on accumulation of osmolytes and antioxidant compounds in cherry tomato. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 43(1), 1–11. https://doi.org/10.15835/nbha4319793

Al Kharusi, L. A., Assaha, D. V. M., Al-Yahyai, R., &Yaish, M. W. (2017). Screening of date palm (Phoenix dactylifera L.) cultivars for salinity tolerance. Forests, 8(4), 136. https://doi.org/10.3390/f8040136

Amini, F., & Ehsanpour, A. A. (2005). Soluble Proteins, Proline, Carbohydrates and Na+/K+ Changes in Two Tomato (Lycopersicon esculentum Mill.) Cultivars under in vitro Salt Stress. American Journal of Biochemistry and Biotechnology, 1(4), 212–216. https://doi.org/10.3844/ajbbsp.2005.212.216

Azevedo, R.A., Alas, R.M., Smith, R.J. (1998). Responses of antioxidant enzymes to transfer from elevated carbon dioxide to air and ozone fumigation, in the leaves androots of wild type and catalase-deficient mutant of barley. Physiologia Plantarum, 104, 280–292. https://doi.org/10.1034/j.1399-3054.1998.1040217.x

Baghalian, K., Haghiry, A., Naghavi, M. R., & Mohammadi, A. (2008). Effect of saline irrigation water on agronomical and phytochemical characters of chamomile (Matricaria recutita L.). Scientia Horticulturae, 116(4), 437–441. https://doi.org/10.1016/j.scienta.2008.02.014

Bates, L., Waldren, S., R. P. Teare, & Rapid, I. D. (1973). Determination of free proline for water stress studies. Plant Soil, 39, 205–207. https://doi.org/10.1007/BF00018060

Ben Abdallah, M., Methenni, K., Nouairi, I., Zarrouk, M., & Youssef, N. Ben. (2017). Drought priming improves subsequent more severe drought in a drought-sensitive cultivar of olive cv. Chétoui. Scientia Horticulturae, 221(September 2016), 43–52. https://doi.org/10.1016/j.scienta.2017.04.021

Bradford, M. M., Dong, Y. Y., Xu, L., Liu, S., & Bai, X. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1–2), 248–254. https://doi.org/10.1016/0003-2697(76)90527-3

Chae, M. J., Lee, J. S., Nam, M. H., Cho, K., Hong, J. Y., Yi, S. A., Suh, S. C., & Yoon, I. S. (2007). A rice dehydration-inducible SNF1-related protein kinase 2 phosphorylates an abscisic acid responsive element-binding factor and associates with ABA signaling. Plant Molecular Biology, 63(2), 151–169. https://doi.org/10.1007/s11103-006-9079-x

Chen, Z., Zhu, D., Wu, J., Cheng, Z., Yan, X., Deng, X., & Yan, Y. (2018). Identification of differentially accumulated proteins involved in regulating independent and combined osmosis and cadmium stress response in Brachypodium seedling roots. Scientific Reports, 8(1), 1–17. https://doi.org/10.1038/s41598-018-25959-8

Davies, M. J. (2016). Protein oxidation and peroxidation. Biochemical Journal, 473(7), 805–825. https://doi.org/10.1042/BJ20151227

De Lacerda, C. F., Cambraia, J., Oliva, M. A., & Ruiz, H. A. (2005). Changes in growth and in solute concentrations in sorghum leaves and roots during salt stress recovery. Environmental and Experimental Botany, 54(1), 69–76. https://doi.org/10.1016/j.envexpbot.2004.06.004

De Smet, I., & Zhang, H. (2013). Abscisic acid in root growth and development. In Plant Roots: The Hidden Half, Vol. 16. eds A. Eshel and T. Beeckman (Boca Raton: CRC Press), (pp. 1–13.).

Dhawi, F., & Al-khayri, J. M. (2008). Proline Accumulation in Response to Magnetic Fields in Date Palm (Phoenix dactylifera L.). Agriculture, 2(1), 80–83. https://doi.org/10.2174/1874331500802010080

Dubois, M., Gilles, K.A., Hamilton, J. K., Rebers, P.A. & Smith, F. (1951). Colourimetric determination of sugars and related substances. Analytical chemistry, 26, 351–356.

El Rabey, H. A., Al-Malki, A. L., & Abulnaja, K. O. (2016). Proteome Analysis of Date Palm (Phoenix dactylifera L.) under Severe Drought and Salt Stress . International Journal of Genomics, 2016, 1–8. https://doi.org/10.1155/2016/7840759

Elsafy, M., Garkava-Gustavsson, L., & Mujaju, C. (2015). Phenotypic Diversity of Date Palm Cultivars (Phoenix dactylifera L.) from Sudan Estimated by Vegetative and Fruit Characteristics . International Journal of Biodiversity, 2015(1), 1–7. https://doi.org/10.1155/2015/610391

Elsheery, N.I., & Cao, C.F. (2008). Gas exchange, chlorophyll fluorescence, and osmotic adjustment in two mango cultivars under drought stress. Acta Physiologiae Plantarum, 30(6), 769–777. https://doi.org/10.1007/s11738-008-0179-x

Elsheery, N.I., Helaly, M.N., Omar, S.A., John, S.V.S., & Zabochnicka-Swiątek, M. (2020). Physiological and molecular mechanisms of salinity tolerance in grafted cucumber. South African Journal of Botany, 130, 90-102. https://doi.org/10.1016/j.sajb.2019.12.014

Esterbauer, H.K. & Cheeseman, H. (1990). Determination of aldehydic lipid peroxidation products: malonalde- hyde and 4-hydroxynonenal. Methods in Enzymology, 186. 407–421. https://doi.org/10.1016/0076-6879(90)86134-H

Ghatak, A., Chaturvedi, P., & Weckwerth, W. (2017). Cereal Crop Proteomics: Systemic Analysis of Crop Drought Stress Responses Towards Marker-Assisted Selection Breeding. Frontiers in Plant Science, 8(June), 1–25. https://doi.org/10.3389/fpls.2017.00757

Hellal, F. A., El-Shabrawi, H. M., Abd El-Hady, M., Khatab, I. A., El-Sayed, S. A. A., & Abdelly, C. (2018). Influence of PEG induced drought stress on molecular and biochemical constituents and seedling growth of Egyptian barley cultivars. Journal of Genetic Engineering and Biotechnology, 16(1), 203–212. https://doi.org/10.1016/j.jgeb.2017.10.009

Helaly, M.N., El-Sheery, N.I., El-Hoseiny, H., Rastogi, A., & Kalaji, H.M. (2018). Impact of treated wastewater and salicylic acid on physiological performance, malformation and yield of two mango cultivars. Scientia Horticulturae, 233, 159-177. https://doi.org/10.1016/j.scienta.2018.01.001

Huang, H., Ullah, F., Zhou, D. X., Yi, M., & Zhao, Y. (2019). Mechanisms of ROS regulation of plant development and stress responses. Frontiers in Plant Science, 10(June), 1–10. https://doi.org/10.3389/fpls.2019.00800

Huseynova, I. M., Aliyeva, D. R., & Aliyev, J. A. (2013). Plant responses to stresses: Role of ascorbate peroxidase in the antioxidant protection. Peroxidases: Biochemical Characteristics, Functions and Potential Applications, 4, 142–158.

Jaleel, C.A., P. Manivannan, A. Wahid, M., & Farooq, R. S. (2009). Drought Stress in Plants : A Review on Morphological Characteristics and Pigments Composition. International Journal of Agriculture, 11, 100–105. https://doi.org/08–305/IGC-DYT/2009/11–1–100–105

Kawamura, T., & Muraoka, I. (2018). Exercise-induced oxidative stress and the effects of antioxidant intake from a physiological viewpoint. Antioxidants, 7(9), 119; https://doi.org/10.3390/antiox7090119

Khan, A., Khan, A. L., Imran, M., & Shahzad, R. (2020a). Silicon and gibberellins : synergistic function in harnessing ABA signaling and heat stress tolerance in date palm (Phoenix dactylifera L.). Plants, 9(May), 620. https://doi.org/10.3390/plants9050620

Khan, A., Khan, A. L., Muneer, S., Kim, Y. H., Al-Rawahi, A., & Al-Harrasi, A. (2019). Silicon and salinity: Crosstalk in crop-mediated stress tolerance mechanisms. Frontiers in Plant Science, 10(October). https://doi.org/10.3389/fpls.2019.01429

Khan, A., Numan, M., Khan, A. L., Lee, I. J., Imran, M., Asaf, S., & Al-Harrasi, A. (2020b). Melatonin: Awakening the defense mechanisms during plant oxidative stress. Plants, 9(4). https://doi.org/10.3390/plants9040407

Khedr, A. H. A., Abbas, M. A., Abdel Wahid, A. A., Quick, W. P., & Abogadallah, G. M. (2003). Proline induces the expression of salt-stress-responsive proteins and may improve the adaptation of Pancratium maritimum L. to salt-stress. Journal of Experimental Botany, 54(392), 2553–2562. https://doi.org/10.1093/jxb/erg277

Komatsu, S., & Hossain, Z. (2013). Organ-specific proteome analysis for identification of abiotic stress response mechanism in crop. Frontiers in Plant Science, 4(April), 1–9. https://doi.org/10.3389/fpls.2013.00071

Kurutas, E. B. (2016). The importance of antioxidants which play the role in cellular response against oxidative/nitrosative stress: Current state. Nutrition Journal, 15(1), 1–22. https://doi.org/10.1186/s12937-016-0186-5

Laemmli, U. (1970). Cleavage of structural proteins during the assembly of the head bacteriophage T4. Nature, 227, 680–685. https://doi.org/10.1038/227680a0

Mittler, R., & Blumwald, E. (2015). The roles of ROS and ABA in systemic acquired acclimation. Plant Cell, 27(1), 64–70. https://doi.org/10.1105/tpc.114.133090

Naeem, M., Nasir Khan, M., A., M., Khan, & Moinuddin, A. (2013). Adverse effects of abiotic stresses on medicinal and aromatic plants and their alleviation by calcium. In N. Tuteja & S. Singh Gill (Eds.), Plant Acclimation to Environmental Stress (pp. 1–493). © Springer Science+Business Media New York. https://doi.org/10.1007/978-1-4614-5001-6

Nakano, Y., & Asada, K. (1981). Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiology, 22(8), 67–80.

Omar, S.A., Elsheery, N.I., Elzaawely, A.A., Strobel, W., & MKalaji, H. (2018). Over Expression of Jatropha’s Dehydrin Jcdhn-2 Enhances Tolerance to Water Stress in Rice Plants. International Journal of Biosciences, 13(2), 53-60.

Omar, S.A., Elsheery, N.I., Kalaji, H.M., Xu, Z.F. Song-Quan, S., Carpentier, R., (2012). Dehydroascorbate reductase and glutathione reductase play an important role in scavenging hydrogen peroxide during natural and artificial dehydration of Jatropha curcas seeds. Journal of Plant Biology, 55(6), 469-480. https://doi.org/10.1007/s12374-012-0276-7

Patankar, H. V., Al-Harrasi, I., Al-Yahyai, R., & Yaish, M. W. (2018). Identification of candidate genes involved in the salt tolerance of date palm (Phoenix dactylifera L.) Based on a yeast functional bioassay. DNA and Cell Biology, 37(6), 524–534. https://doi.org/10.1089/dna.2018.4159

Paul, S., Gayen, D., Datta, S. K., & Datta, K. (2015). Dissecting root proteome of transgenic rice cultivars unravels metabolic alterations and accumulation of novel stress responsive proteins under drought stress. Plant Science, 234, 133–143. https://doi.org/10.1016/j.plantsci.2015.02.006

Piasecka, A., Kachlicki, P., & Stobiecki, M. (2019). Analytical methods for detection of plant metabolomes changes in response to biotic and abiotic stresses. International Journal of Molecular Sciences, 20(2). https://doi.org/10.3390/ijms20020379

Ponnaiah, G., Gupta, S. K., Blümmel, M., Marappa, M., Pichaikannu, S., Das, R. R., & Rathore, A. (2019). Utilization of molecular marker based genetic diversity patterns in hybrid parents to develop better forage quality multi-cut hybrids in Pearl Millet. Agriculture (Switzerland), 9(5), 97. https://doi.org/10.3390/agriculture9050097

Sagisaka S. (1976). The occurrence of peroxide in a perennial plant Populas gelrica. Plant Physiology, 57, 308–309. https://doi.org/10.1104/pp.57.2.308

Sairanen, I., Novák, O., Pěnčík, A., Ikeda, Y., Jones, B., Sandberg, G., & Ljung, K. (2013). Soluble carbohydrates regulate auxin biosynthesis via PIF proteins in arabidopsis. Plant Cell, 24(12), 4907–4916. https://doi.org/10.1105/tpc.112.104794

Salehin, M., Li, B., Tang, M., Katz, E., Song, L., Ecker, J. R., Kliebenstein, D., & Estelle, M. (2019). Auxin-sensitive Aux/IAA proteins mediate drought tolerance in Arabidopsis by regulating glucosinolate levels. The preprint server for biology, 572305. https://doi.org/10.1101/572305

Shareef, H. J. (2019). Salicylic acid and Potassium Promote Flowering through modulating the hormonal levels and Protein pattern of Date palm Phoenix dactylifera L. Sayer offshoots. Acta Agriculturae Slovenica, 114(2), 231–238. https://doi.org/10.14720/aas.2019.114.2.8

Shareef, H. J., Abdi, G., & Fahad, S. (2020). Change in photosynthetic pigments of Date palm offshoots under abiotic stress factors. Folia oecologica, 47(1), 45–51. https://doi.org/10.2478/foecol-2020-0006

Sofo, A., Scopa, A., Nuzzaci, M., & Vitti, A. (2015). Ascorbate Peroxidase and Catalase Activities and Their Genetic Regulation in Plants Subjected to Drought and Salinity Stresses. International Journal of Molecular Sciences, 16, 13561–13578. https://doi.org/10.3390/ijms160613561

Tang, Y., Wang, L., Ma, C., Liu, J., Liu, B., & Li, H. (2011). The Use of HPLC in Determination of Endogenous Hormones in Anthers of Bitter Melon. Journal of Life Sciences, 5, 139–142.

Tanimoto, E. (2005). Regulation of root growth by plant hormones - Roles for auxin and gibberellin. Critical Reviews in Plant Sciences, 24(4), 249–265. https://doi.org/10.1080/07352680500196108

Vishwakarma, K., Upadhyay, N., Kumar, N., Yadav, G., Singh, J., Mishra, R. K., Kumar, V., Verma, R., Upadhyay, R. G., Pandey, M., & Sharma, S. (2017). Abscisic Acid Signaling and Abiotic Stress Tolerance in Plants: A Review on Current Knowledge and Future Prospects. Frontiers in Plant Science, 08(February), 1–12. https://doi.org/10.3389/fpls.2017.00161

Xu, W., Cui, K., Xu, A., & Nie, L. (2015). Drought stress condition increases root to shoot ratio via alteration of carbohydrate partitioning and enzymatic activity in rice seedlings. Acta Physiologiae Plantarum, 37:9. https://doi.org/10.1007/s11738-014-1760-0

Yaish, M. W., Sunkar, R., Zheng, Y., Ji, B., Al-Yahyai, R., & Farooq, S. A. (2015). A genome-wide identification of the miRNAome in response to salinity stress in date palm (Phoenix dactylifera L.). Frontiers in Plant Science, 6(NOVEMBER), 946. https://doi.org/10.3389/fpls.2015.00946




DOI: http://dx.doi.org/10.14720/aas.2021.117.1.1829

Refbacks

  • There are currently no refbacks.


Copyright (c) 2021 Hussein Shareef

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 

Acta agriculturae Slovenica is an Open Access journal published under the terms of the Creative Commons CC BY License.

                           


eISSN 1854-1941