Document Type : Original Article

Authors

Department of Cell and Molecular Bioology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran

Abstract

Introduction
Abiotic stresses can disrupt future food security, which simultaneously implies the importance of genotype screening in stressed environments. Drought and phosphorus stresses have great effects on the growth and development of maize. Soil dryness and phosphorus deficiency cause similar effects and illicit similar defence mechanisms in plants (Xia et al., 2021a). Drought and phosphorus stresses in the root zone can cause active oxygen accumulation in plants. In order to deal with excessive accumulation of active oxygen, plants activate their oxidative defence mechanisms through enzyme or non-enzymatic routes. Oxidative stress caused by excessive accumulation of reactive oxygen species is one of the important physiological factors affecting plant growth and development under stress conditions. The sensitivity of genotypes to water deficit is different and they can be classified into two groups, tolerant or sensitive. Maize (Zea mays L.) is one of the most important crops in the world for food security, as it feeds millions of people. Abiotic stress can create significant challenges in maize production. The present study aimed to determine the effects of phosphate and PEG stresses on the physiological and biochemical traits in the maize cultivars.
Materials and methods
Measured traits in leaf and root tissues were analysed among five maize cultivars under PEG and phosphate stresses. Also, analysis of biochemical traits such as chlorophyll a/b and carotenoids in maize seedlings under PEG 20% and low phosphate were analysed. The five maize cultivars were exposed to PEG 20% and low phosphate stresses and sampled at two-time points after treatment (24 and 48 h). This experiment was carried out as a factorial experiment in the form of a completely randomized design with three replications. In this study, antioxidant enzymes such as catalase, ascorbate peroxidase, and peroxidase activity were measured in leaf and root tissues. Further, PCA, dandraogram and correlation of physiological traits, biochemical and morphological traits were analysed. Statistical analysis was performed using SPSS. Differences across tissues were analysed using one-way ANOVA. Duncan’s test was used to compare the treatment means at P<0.05. Values represent the means of three replications per treatment. Principal Component Analysis (PCA) and correlations were performed using SPSS 22.
Results and discussion
Based on the cluster analysis, the cultivars were grouped into three classes. The cluster I included Fajr, Paya, and Dehghan whereas, Kosha and Taha cultivars were placed in the clusters II and III, respectively. Also, there was a significantly positive correlation at the probability level of one percent between the content of chlorophyll a/b and root anthocyanin and total chlorophyll content. Correlation between biochemical and physiological traits is shown in Figure 2. The chlorophyll a showed a positive and significant correlation with total chlorophyll and carotenoid contents. The chlorophyll b showed a positive and significant correlation with total chlorophyll content and root anthocyanin. PCA was performed on physiological and biochemical traits to fully investigate the various factors that play essential roles in the drought indices. The cumulative contribution rate of the total changes of PC3 reached 97%. According to PCA analysis measured by correlation matrix and biplot analysis method, it was found that these parameters can be used to evaluate the response of maize genotypes to abiotic stresses under different environments. The relationships between biochemical traits and genotypes is shown graphically in two segments of PC1 and PC2.
Conclusion
Principal component analysis (PCA) and measured traits showed that Fajr, Paya, and Kosha cultivars can show high performance under studied stress conditions. In the present study, the Kosha cultivar was shown to be relatively water stress and low phosphate tolerant due to improved antioxidant, chlorophyll, and carotenoids activities under abiotic stresses.

Keywords

Main Subjects

 Ansari, A., Gharaghani, A., 2019. A comparative study of genetic diversity, heritability and inter-relationships of tree and nut attributes between Prunus scoparia and P. elaeagnifolia using multivariate statistical analysis. International Journal of Horticultural Science and Technology. 6, 137-150.  https://doi.org/10.22059/ijhst.2019.276425.282
Bhargava, S., Sawant, K., 2013. Drought stress adaptation: metabolic adjustment and regulation of gene expression. Plant Breeding. 132, 21-32. https://doi.org/10.1111/pbr.12004
Brown, L.K., George, T.S., Thompson, J.A., Wright, G., Lyon, J., Dupuy, L., Hubbard, S.F., White, P.J., 2012. What are the implications of variation in root hair length on tolerance to phosphorus deficiency in combination with water stress in barley (Hordeum vulgare)?. Annals of Botany, 110, 319-328. https://doi.org/10.1093/aob/mcs085
Caverzan, A., Casassola, A., Brammer, S.P., 2016. Antioxidant responses of wheat plants under stress. Genetics and molecular biology. 39,1-6. https://doi.org/10.1590/1678-4685-GMB-2015-0109
Chance, B., Maehly, A.C., 1955. Assay of Catalase and Peroxidase. Methods in Enzymology, 2, 764-775. https://doi.org/10.1016/S0076-6879(55)02300-8
Chazen, O., Neumann, P.M., 1994. Hydraulic signals from the roots and rapid cell-wall hardening in growing maize (Zea mays L.) leaves are primary responses to polyethylene glycol-induced water deficits. Plant Physiology. 104, 1385-1392. https://doi.org/10.1104/pp.104.4.1385
Cheng, L., Bucciarelli, B., Liu, J., Zinn, K., Miller, S., Patton-Vogt, J., Allan, D., Shen, J. and Vance, C.P., 2011. White lupin cluster root acclimation to phosphorus deficiency and root hair development involve unique glycerophosphodiester phosphodiesterases. Plant Physiology. 156, 1131-1148. https://doi.org/10.1104/pp.111.173724
Cordell, D., Rosemarin, A., Schröder, J.J., Smit, A.L., 2011. Towards global phosphorus security: A systems framework for phosphorus recovery and reuse options. Chemosphere. 84, 747-758. https://doi.org/10.1016/j.chemosphere.2011.02.032
Dalal, V.K., Tripathy, B.C., 2012. Modulation of chlorophyll biosynthesis by water stress in rice seedlings during chloroplast biogenesis. Plant, Cell & Environment. 35, 1685-1703. https://doi.org/10.1111/j.1365-3040.2012.02520.x
Dumont, S., Rivoal, J., 2019. Consequences of oxidative stress on plant glycolytic and respiratory metabolism. Frontiers in Plant Science. 10, 166. https://doi.org/10.3389/fpls.2019.00166
Ekinci, M., Ors, S., Yildirim, E., Turan, M.E.T.I.N., Sahin, U., Dursun, A., Kul, R., 2020. Determination of physiological indices and some antioxidant enzymes of chard exposed to nitric oxide under drought stress. Russian Journal of Plant Physiology. 67, 740-749. https://doi.org/10.1134/S1021443720040056
Elanchezhian, R., Krishnapriya, V., Pandey, R., Rao, A.S., Abrol, Y.P., 2015. Physiological and molecular approaches for improving phosphorus uptake efficiency of crops. Current Science. 108, 1271-1279. https://www.jstor.org/stable/24905488
Fei, X., Li, J., Kong, L., Hu, H., Tian, J., Liu, Y., Wei, A., 2020. miRNAs and their target genes regulate the antioxidant system of Zanthoxylum bungeanum under drought stress. Plant Physiology and Biochemistry. 150, 196-203. https://doi.org/10.1016/j.plaphy.2020.01.040
Filek, M., Walas, S., Mrowiec, H., Rudolphy-Skórska, E., Sieprawska, A. and Biesaga-Kościelniak, J., 2012. Membrane permeability and micro-and macroelement accumulation in spring wheat cultivars during the short-term effect of salinity-and PEG-induced water stress. Acta Physiologiae Plantarum. 34, 985-995. https://doi.org/10.1007/s11738-011-0895-5
Ge, T.D., Sun, N.B., Bai, L.P., Tong, C.L., Sui, F.G., 2012. Effects of drought stress on phosphorus and potassium uptake dynamics in summer maize (Zea mays) throughout the growth cycle. Acta Physiologiae Plantarum. 34, 2179-2186. https://doi.org/10.1007/s11738-012-1018-7
Ghassemi, S., Ghassemi-Golezani, K., Salmasi, S.Z., 2019. Changes in antioxidant enzymes activities and physiological traits of ajowan in response to water stress and hormonal application. Scientia Horticulturae, 246, 957-964. https://doi.org/10.1016/j.scienta.2018.11.086
Gomez, F.P., Oliva, M.A., Mielke, M.S., de Almeida, A.A.F., Leite, H.G., Aquino, L.A., 2008. Photosynthetic limitations in leaves of young Brazilian Green Dwarf coconut (Cocos nucifera L.‘nana’) palm under well-watered conditions or recovering from drought stress. Environmental and Experimental Botany. 62, 195-204. https://doi.org/10.1016/j.envexpbot.2007.08.006
 Guo, K., Li, Z., Tian, H., Du, X., Liu, Z., Huang, H., Wang, P., Ye, Z., Zhang, X., Tu, L., 2020. Cytosolic ascorbate peroxidases plays a critical role in photosynthesis by modulating reactive oxygen species level in stomatal guard cell. Frontiers in Plant Science, 11,446. https://doi.org/10.3389/fpls.2020.00446
Hajibarat, Z., Saidi, A., Hajibarat, Z., 2022. Genome-Wide Identification of 14-3-3 Gene family and characterization of their expression in developmental stages of Solanum tuberosum under multiple biotic and abiotic stress conditions. Functional & Integrative Genomics. 6, 1377-1390. https://doi.org/10.1007/s10142-022-00895-z
Hasanuzzaman, M., Parvin, K., Bardhan, K., Nahar, K., Anee, T.I., Masud, A.A.C., Fotopoulos, V., 2021. Biostimulants for the regulation of reactive oxygen species metabolism in plants under abiotic stress. Cells. 10, 2537. https://doi.org/10.3390/cells10102537
He, Z., Zhao, T., Yin, Z., Liu, J., Cheng, Y., Xu, J., 2020. The phytochrome-interacting transcription factor CsPIF8 contributes to cold tolerance in citrus by regulating superoxide dismutase expression. Plant Science, 298, p.110584. https://doi.org/10.1016/j.plantsci.2020.110584
Hellal, F.A., El-Shabrawi, H.M., Abd El-Hady, M., Khatab, I.A., El-Sayed, S.A.A. and 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, 203-212.
Hernández-Pérez, C.A., Gómez-Merino, F.C., Spinoso-Castillo, J.L., Bello-Bello, J.J., 2021. In vitro screening of sugarcane cultivars (Saccharum spp. hybrids) for tolerance to polyethylene glycol-induced water stress. Agronomy. 11, 598. https://doi.org/10.3390/agronomy11030598
Jackson, R.B., Sperry, J.S., Dawson, T.E., 2000. Root water uptake and transport: using physiological processes in global predictions. Trends in Plant Science, 5, 482-488. https://doi.org/10.1016/S1360-1385(00)01766-0
Ji, H., Liu, L., Li, K., Xie, Q., Wang, Z., Zhao, X., Li, X., 2014. PEG-mediated osmotic stress induces premature differentiation of the root apical meristem and outgrowth of lateral roots in wheat. Journal of Experimental Botany. 65, 4863-4872. https://doi.org/10.1093/jxb/eru255
Kolarovic, L., Valentovič, P., Luxová, M., Gašparíková, O., 2009. Changes in antioxidants and cell damage in heterotrophic maize seedlings differing in drought sensitivity after exposure to short-term osmotic stress. Plant Growth Regulation. 59, 21-26. https://doi.org/10.1007/s10725-009-9384-x
Kosturkova, G., Todorova, R., Sakthivelu, G., Akitha Devi, M.K., Giridhar, P., Rajasekaran, T., Ravishankar, G.A., 2008. Response of Bulgarian and Indian soybean genotypes to drought and water deficiency in field and laboratory conditions. General and Applied Plant Physiology. 34, 239-250.
Kukreja, S., Nandwal, A.S., Kumar, N., Sharma, S.K., Sharma, S.K., Unvi, V., Sharma, P.K., 2005. Plant water status, H2O2 scavenging enzymes, ethylene evolution and membrane integrity of Cicer arietinum roots as affected by salinity. Biologia Plantarum. 49,305-308. https://doi.org/10.1007/s10535-005-5308-4
Lahlou, O., Ouattar, S., Ledent, J.F., 2003. The effect of drought and cultivar on growth parameters, yield and yield components of potato. Agronomie, 23, 257-268. https://doi.org/10.1051/agro:2002089
Li, L., Zhao, X., Manthiram, A., 2012. A dual-electrolyte rechargeable Li-air battery with phosphate buffer catholyte. Electrochemistry Communications. 14, 78-81. https://doi.org/10.1016/j.elecom.2011.11.007
Li, R., Zeng, Y., Xu, J., Wang, Q., Wu, F., Cao, M., Lan, H., Liu, Y., Lu, Y., 2015. Genetic variation for maize root architecture in response to drought stress at the seedling stage. Breeding Science. 65, 298-307. https://doi.org/10.1270/jsbbs.65.298
Lima, A.L.S., DaMatta, F.M., Pinheiro, H.A., Totola, M.R., Loureiro, M.E., 2002. Photochemical responses and oxidative stress in two clones of Coffea canephora under water deficit conditions. Environmental and Experimental Botany. 47, 239-247. https://doi.org/10.1016/S0098-8472(01)00130-7
Lipiec, J., Doussan, C., Nosalewicz, A., Kondracka, K., 2013. Effect of drought and heat stresses on plant growth and yield: a review. International Agrophysics. 27. https://doi.org/10.2478/intag-2013-0017
Lipkovich, I.A., Smith, E.P., 2002. Biplot and singular value decomposition macros for Excel©. Journal of statistical software, 7, 1-15. https://doi.org/10.18637/jss.v007.i05
Liu, W.J., Zhu, Y.G., Smith, F.A., Smith, S.E., 2004. Do phosphorus nutrition and iron plaque alter arsenate (As) uptake by rice seedlings in hydroponic culture?. New Phytologist, 162, 481-488. https://doi.org/10.1111/j.1469-8137.2004.01035.x
Mallik, S., Nayak, M., Sahu, B.B., Panigrahi, A.K., Shaw, B.P., 2011. Response of antioxidant enzymes to high NaCl concentration in different salt-tolerant plants. Biologia Plantarum, 55, 191-195. https://doi.org/10.1007/s10535-011-0029-3
Meng, X., Chen, W.W., Wang, Y.Y., Huang, Z.R., Ye, X., Chen, L.S., Yang, L.T., 2021. Effects of phosphorus deficiency on the absorption of mineral nutrients, photosynthetic system performance and antioxidant metabolism in Citrus grandis. PLoS One. 16, p.e0246944. https://doi.org/10.1371/journal.pone.0246944
Mihaljević, I., Viljevac Vuletić, M., Šimić, D., Tomaš, V., Horvat, D., Josipović, M., Zdunić, Z., Dugalić, K., Vuković, D., 2021. Comparative study of drought stress effects on traditional and modern apple cultivars. Plants. 10, 561. https://doi.org/10.3390/plants10030561
Mitra, J., 2001. Genetics and genetic improvement of drought resistance in crop plants. Current Science. 758-763. https://www.jstor.org/stable/24105661
Mittler, R., 2002. Oxidative stress, antioxidants and stress tolerance. Trends in plant science, 7, 405-410. https://doi.org/10.1016/S1360-1385(02)02312-9
Motamadi, M., Banisaidi, A., 2022. Evaluation of Yield, Some Physiological Properties and Drought Tolerance Evaluation of Barley (Hordeum vulgare L.) Cultivars in Khuzestan Province. Journal of Plant Production Sciences, 12, 211-193. [In Persian with English Summary]. http://doi.org/10.22059/IJFCS.2019.264529.654518
Muscolo, A., Sidari, M., Anastasi, U., Santonoceto, C., Maggio, A., 2014. Effect of PEG-induced drought stress on seed germination of four lentil genotypes. Journal of Plant Interactions. 9, 354-363. https://doi.org/10.1080/17429145.2013.835880
Naderi, R., Valizadeh, M., Toorchi, M., Shakiba, M.R., 2014. Antioxidant enzyme changes in response to osmotic stress in wheat (Triticum aestivum L.) seedling. Acta Biologica Szegediensis. 58, 95-101.
Nakano, Y., Asada, K., 1981. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiology. 22, 867-880. https://doi.org/10.1093/oxfordjournals.pcp.a076232
Obidiegwu, J.E., Bryan, G.J., Jones, H.G., Prashar, A., 2015. Coping with drought: stress and adaptive responses in potato and perspectives for improvement. Frontiers in Plant Science. 6, 542. https://doi.org/10.3389/fpls.2015.00542
Peršić, V., Ament, A., Antunović Dunić, J., Drezner, G., Cesar, V., 2022. PEG-induced physiological drought for screening winter wheat genotypes sensitivity–integrated biochemical and chlorophyll a fluorescence analysis. Frontiers in Plant Science. 13, 987702.
Plaxton, W.C., Tran, H.T., 2011. Metabolic adaptations of phosphate-starved plants. Plant Physiology. 156, 1006-1015. https://doi.org/10.1104/pp.111.175281
Rauf, M., Munir, M., ul Hassan, M., Ahmad, M., Afzal, M., 2007. Performance of wheat genotypes under osmotic stress at germination and early seedling growth stage. African Journal of Biotechnology. 6.
Robin, A.H.K., Uddin, M.J., Bayazid, K.N., 2015. Polyethylene glycol (PEG)-treated hydroponic culture reduces length and diameter of root hairs of wheat varieties. Agronomy. 5, 506-518. https://doi.org/10.3390/agronomy5040506
Sairam, R.K., Rao, K.V., Srivastava, G.C., 2002. Differential response of wheat genotypes to long term salinity stress in relation to oxidative stress, antioxidant activity and osmolyte concentration. Plant Science. 163, 1037-1046. https://doi.org/10.1016/S0168-9452(02)00278-9
Sardans, J., Peñuelas, J., 2012. The role of plants in the effects of global change on nutrient availability and stoichiometry in the plant-soil system. Plant Physiology. 160, 1741-1761. https://doi.org/10.1104/pp.112.208785
Schütz, M., Fangmeier, A., 2001. Growth and yield responses of spring wheat (Triticum aestivum L. cv. Minaret) to elevated CO2 and water limitation. Environmental Pollution. 114, 187-194. doi: 10.1016/s0269-7491(00)00215-3
Sharma, P., Dubey, R.S., 2005. Modulation of nitrate reductase activity in rice seedlings under aluminium toxicity and water stress: role of osmolytes as enzyme protectant. Journal of Plant Physiology. 162, 854-864. https://doi.org/10.1016/j.jplph.2004.09.011
Shavrukov, Y., Kurishbayev, A., Jatayev, S., Shvidchenko, V., Zotova, L., Koekemoer, F., De Groot, S., Soole, K., Langridge, P., 2017. Early flowering as a drought escape mechanism in plants: how can it aid wheat production?. Frontiers in Plant Science. 8, 1950. https://doi.org/10.3389/fpls.2017.01950
Sheteiwy, M.S., Abd Elgawad, H., Xiong, Y.C., Macovei, A., Brestic, M., Skalicky, M., Shaghaleh, H., Alhaj Hamoud, Y., El‐Sawah, A.M., 2021. Inoculation with Bacillus amyloliquefaciens and mycorrhiza confers tolerance to drought stress and improve seed yield and quality of soybean plant. Physiologia Plantarum. 172, 2153-2169. https://doi.org/10.1111/ppl.13454
Shi, G., Xia, S., Ye, J., Huang, Y., Liu, C. and Zhang, Z., 2015. PEG-simulated drought stress decreases cadmium accumulation in castor bean by altering root morphology. Environmental and Experimental Botany. 111, 127-134. https://doi.org/10.1016/j.envexpbot.2014.11.008
Wagner, GJ., 1979. Content and vacuole/extravacuole distribution of neutral sugars, free amino acids, and anthocyanin in protoplasts. Plant Physiology. 64, 88-93. https://doi.org/10.1104/pp.64.1.88
Wissuwa, M., Gamat, G., Ismail, A.M., 2005. Is root growth under phosphorus deficiency affected by source or sink limitations? Journal of Experimental Botany. 56, 1943-1950. https://doi.org/10.1093/jxb/eri189
Xia, Z., Zhang, G., Zhang, S., Wang, Q., Fu, Y., Lu, H., 2021. Efficacy of root zone temperature increase in root and shoot development and hormone changes in different maize genotypes. Agriculture. 11, 477. https://doi.org/10.3390/agriculture11060477
Xia, Z., Zhang, S., Wang, Q., Zhang, G., Fu, Y., Lu, H., 2021. Effects of root zone warming on maize seedling growth and photosynthetic characteristics under different phosphorus levels. Frontiers in Plant Science, 12, 746152. https://doi.org/10.3389/fpls.2021.746152
Yaghotipoor, A., Farshadfar, E., Saeidi, M., 2017. Evaluation of phenotypic stability in bread wheat accessions using parametric and non-parametric methods. The Journal of Animal & Plant Sciences, 27, 1269-1275.
Yang, S., Ulhassan, Z., Shah, A.M., Khan, A.R., Azhar, W., Hamid, Y., Hussain, S., Sheteiwy, M.S., Salam, A., Zhou, W., 2021. Salicylic acid underpins silicon in ameliorating chromium toxicity in rice by modulating antioxidant defense, ion homeostasis and cellular ultrastructure. Plant Physiology and Biochemistry, 166, 1001-1013. https://doi.org/10.1016/j.plaphy.2021.07.013
Yang, G., Yu, L., Zhang, K., Zhao, Y., Guo, Y., Gao, C., 2017. A ThDREB gene from Tamarix hispida improved the salt and drought tolerance of transgenic tobacco and T. hispida. Plant Physiology and Biochemistry, 113, 187-197. https://doi.org/10.1016/j.plaphy.2017.02.007
Zhang, K., Liu, H., Tao, P., Chen, H., 2014. Comparative proteomic analyses provide new insights into low phosphorus stress responses in maize leaves. PLoS One, 9, e98215. https://doi.org/10.1371/journal.pone.0098215
Zhu, X.G., Long, S.P., Ort, D.R., 2010. Improving photosynthetic efficiency for greater yield. Annual review of plant biology, 61, 235-261.  https://doi.org/10.1146/annurev-arplant-042809-112206