Document Type : Original Article

Authors

1 Ph.D. student, Dept. of Plant Production and Genetics, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran

2 Dept. of Plant Production and Genetics, Faculty of Agriculture and Natural Resources, University of Mohaghegh Ardabili, Ardabil, Iran

3 Horticulture Crops Research Department, Ardabil Agricultural and Natural Resources Research Centre, AREEO, Ardabil, Iran

4 Meshgin Shahr Faculty of Agriculture, University of Mohaghegh Ardabili, Meshgin Shahr, Iran

Abstract

Introduction
Potato is an important food crop with high yields. However, when exposed to drought it suffers major yield losses. Considering its global importance and the increasing incidence of drought due to climate change, research toward drought tolerance in potatoes remains imperative. In vertebrates, estrogen, and androgen steroidal hormones have important functions in development and reproduction. Estrogens and estrogen-like compounds (xenoestrogens) from livestock manure, animal waste, and human waste (especially pharmaceutical waste), are being disposed of and excreted at high rates into the agricultural soil and groundwater all over the world. The aim of this study was to investigate the effect of the β-estradiol application on the tolerance of different potato genotypes to water deficit stress.
 
Materials and Methods
To study the effect of β-estradiol application in enhancement of drought tolerance in different potato genotypes, an experiment was conducted as a factorial split-plot arrangement with three replications in the greenhouse of Zare Gostar Arta Technology Company in Ardabil. Treatment of drought stress was reducing the amount of irrigation water (100, 60, and 40% of available water) and β-estradiol hormone at three levels of zero (control), 10-6 and 10-12 molar both in the main plots and 10 potato genotypes were placed in sub-plots. In the present study plant height, leaf relative water content, number of tubers per plant, tubers weight per plant, mean tubers weight, reducing sugar percentage, dry matter percent, protein tubers percent, starch percent, proline content, superoxide dismutase, catalase activity, and polyphenol oxidase were measured. Data were analyzed by using SAS software, 9.2, and also the mean of the studied traits were compared by LSD test at 5% probability level.
 
 Results and discussion
The results of the analysis of variance showed that there was a significant difference among the drought levels in terms of all studied traits. Difference between β-estradiol levels in terms of plant height, number of tubers per plant, the weight of tubers per plant, mean tuber weight, the relative water content of leaves, tuber dry matter percent, protein tuber percent, percentage of starch, and catalase, polyphenol oxidase and superoxide dismutase contents was significant. Interaction effect of drought and hormone on plant height, tuber weight per plant, mean tuber weight, number of tubers per plant, tuber dry matter percent, the relative water content of leaves, reducing sugar percent, starch percent, catalase and polyphenol oxidase was significant. There was a significant difference between the studied genotypes in terms of all studied traits. Interaction effect of genotype × drought on plant height, the relative leaf water content, number of tubers per plant, tuber weight per plant, mean tuber weight, tuber dry matter percentage, protein percent, starch percent, proline content, catalase, and superoxide dismutase was also significant. Finally, the interaction of genotype × hormone on plant height, relative leaf water content, number of tubers per plant, tuber weight per plant, tuber weight mean, dry matter percent, protein percent and catalase content was significant. In all three drought levels, the highest number of tubers per plant allocated to two genotypes of G3 and G6. The highest relative water content was assigned to the G6 genotype, the highest percentage of regenerating sugar and the percentage of the dry matter assigned to the G3 genotype and the highest plant height, the percentage of starch and the percentage of protein assigned to the G4 genotype.
The results showed that under normal conditions, G6, G4, and G3 genotypes (with an average of 96.90, 93.77, and 92.04 g/plant respectively) had the highest tuber weight per plant. In drought treatment of 60% of usable water supply, although the highest tuber weight was assigned to G1 genotype, there was no significant differences between the mentioned genotype and G2, G3, G5, and G6 genotypes. Also, in drought treatment of 40% of usable water supply, there was only significantly difference between G6 and G9 genotypes. In this study, the use of β-estradiol (especially the level of 10-12 molar) in all three water deficit treatments significantly increased the plant height, mean tuber weight, relative water content, dry matter percentage, starch percentage, proline, catalase and polyphenol oxidase contents as compared with the control. Finally, the highest plant height, number of tubers per plant, tubers weight per plant, dry matter percentage, and protein content were assigned to the G4 genotype with 10-12 molar of β-estradiol. Finally, among the studied genotypes, G4 at the level of 10-12 (with an average of 62.21 g/plant) had the highest tuber weight per plant.
 
Conclusions
 Based on the results of the present study, it can be stated that both G3 and G6 genotypes can be promising genotypes for cultivation under normal conditions and mild drought stress in the study area. In the drought treatment of 40% of usable water supply, only a significant difference was seen between G6 and G9 genotypes. It can be concluded that the response of the 10 genotypes to severe drought stress conditions was almost similar. Also, the genetic potential of G4 and G6 genotypes for uptake and use of β-estradiol was higher compared to other genotypes. Furthermore, the use of β-estradiol hormone can improve the quantitative and qualitative characteristics of potato genotypes under water deficit conditions.
 

Keywords

Main Subjects

Agili, S., Aggrey, B.N., Ngamau, K., Masinde, W.P., 2015. In vitro evaluation of orange-fleshed sweet potato genotypes for drought tolerance using polyethylene glycol. Potato and Sweet Potato in Africa: Transforming the Value Chains for Food and Nutrition Security. 30th June to 4th July 20139, the Triennial Conference of APA, Naivasha, Kenya
Ayas, S., 2013. The effects of different regimes on potato (Solanum tuberosum L. Hermes) yield and quality characteristics under unheated greenhouse conditions. Bulgarian Journal of Agricultural Science. 19, 87-95.
Ayas, S., Korukcu, A., 2010. Water-yield relationships in deficit irrigated potato. Journal of Agricultural Faculty of Uludag University. 24, 23-26.
Bates, L.S., Waldren, R.P., Teare, I.D., 1973. Rapid determination of free proline for water stress studies. Plant and Soil. 39, 205-207.
Bhattacharya, B., Gupta, K., 1981. Steroid hormone effects on growth and apical dominance of sunflower. Phytochemistry. 20, 989-991.
Bradford, M.M., 1976. A rapid and sensitive method for the qualify cation of microgram quantities of protein utilizing the principle of protein dye binding. Analytical Biochemistry. 72, 248-254.
 Brown, C., 2006. The effects of estrogen on the growth and tuberization of potato plants (Solanum tuberosum cv. ‘Iwa’) grown in liquid tissue culture media. A thesis for the Degree of Master of Science in Plant Biotechnology. University of Canterbury School of Biological Sciences. 128P
Cantore, V., Wassar, F., Yamaç, S.S., Sellami, M. H., Albrizio, R., Stellacci, A.M., Todorovic, M., 2014. Yield and water use efficiency of early potato grown under different irrigation regimes. International Journal of Plant Production. 8, 409-428.
Carli, C., Yuldashev, F., Khalikov, Condori, B., Mares, V., and Monneveux, A., 2014. Effects of different irrigation regimes on yield, water use efficiency and quality of potato in the lowlands of Tashkent, Uzbekistan: A field and modeling perspective. Field Crops Research 163, 90-99.
Carreau, S., Delalande, C., Silandre, D., Bourguiba, S. Lambard, S., 2004. Aromatase and estrogen receptors in male reproduction. Molecular and Cellular Endocrinology. 246, 65-68.
Chance, B., Maehley, A., 1955. Assay of catalases and peroxidase, Methods in Enzymology. 2, 764–775.
Chaoui, A., El Ferjani, E., 2013. β-Estradiol protects embryo growth from heavy-metal toxicity in germinating lentil seeds. Journal of Plant Growth Regulation. 32, 1-16.
Chaves, M.M., Maroco, J.P., Pereira, J.S., 2003. Understanding plant responses to drought from genes to the whole plant. Functional Plant Biology. 30, 239-264.
Choudhary, S.P., Oral, H.V., Bhardwaj, R., Yu, J.Q., Tran, L.S.P. 2012. Interaction of brassinosteroids and polyamines enhances copper stress tolerance in Raphanus sativus. Journal of Experimental Botany. 63, 5659–5675
Crusciol, C.A.C., Pulz, A.L., Lemos, L.B., Soratto, R.P. Lima, G.P.P., 2009. Effects of silicon and drought stress on tuber yield and leaf biochemical characteristics in potato. Crop Science. 49, 949-954.
Eisenbarth D.A., Weig A.R., 2005. Dynamics of aquaporins and water relations during hypocotyl elongation in Ricinus communis L. seedlings. Journal of Experimental Botany. 56, 1831–1842.
Erdal S., 2011. Alleviation of salt stress in wheat seedlings by mammalian sex hormones, Journal of the Science of Food and Agriculture. 92, 1411-1416.
Erdal, S., 2012a. Androsterone-induced molecular and physiological changes in maize seedlings in response to chilling stress. Plant Physiology and Biochemistry. 57, 1-7.
Erdal, S., 2012b. Exogenous mammalian sex hormones mitigate inhibition in growth by enhancing antioxidant activity and synthesis reactions in germinating maize seeds under salt stress. Journal of the Science of Food and Agriculture. 92, 839-843
Erdal, S., Dumlupinar, R., 2011. Mammalian sex hormones stimulate antioxidant system and enhance growth of chickpea plants. Acta Physiologiae Plantarum. 33, 1011–1017
Food and Agriculture Organization. 2018. FAOSTAT, Retrieved January 12, 2018, from http://faostat.fao.org/site/291/default.aspx. (Accessed 10 September 2018).
Giannopolitis, C.N., Ries. S.K., 1977. Superoxide dismutases I. occurrence in higher plants. Plant Physiology. 59, 309-14.
 Golestani Kermani, S., Nouri Imamzadehei, M., Shayannezhad, M., Shahnazari, A., Mohammadkhani, A., 2014. Effects of water stress on quantitative and qualitative properties of potato crop (c.v. Agria) in deficit irrigation and partial root zone drying techniques. Journal of Irrigation Sciences and Engineering, 37, 123-135.
Gu F., Hata R., Toku K., Yang L., Ma Y.J., Maeda, N., 2003. Testosterone up-regulates aquaporin-4 expression in cultured astrocytes. Journal of Neuroscience Research. 72, 709-715.
Hamzehei, R., Davtyan, V. A., Ghobadi, M. E., Parvizi, KH., Ghadami-Firoozabadi, A., 2017. Effect of deficit irrigation on some physiological characteristics and yield in two potato (Solanum tuberosum L.) cultivars. Plant Production Technology. 17, 15-26. [In Persian with English summary]
Hanselman, T.A., Graetz, D.A. Wilkie, A.C., 2003. Manure-borne estrogens as potential environmental contaminants: A review. Environmental Science and Technology. 37, 5471-5478.
Hassanpanah, D., 2009. In vitro and in vivo screening of potato cultivars plantlets against water stress by polyethylene glycol and potassium humate. Biotechnology. 8, 132-137.
Hassanpanah, D., 2010. Evaluation of potato advanced cultivars against water deficit stress under in vitro and in vivo condition. Biotechnology. 9, 164-169.
Hassanpanah, D., Asghari Zakaria, R., 2018. Evaluation of radiated potato genotypes with gamma rays in water deficit stress. Agricultural Science and Sustainable Production. 28, 107-122. [In Persian with English summary].
Hassanpanah, D., Hassanabadi, H., 2011. Evaluating tolerance of potato cultivars and promising clones to water deficit in Ardabil region. Journal of Crop and Weed Ecophysiology. 4, 1-18. [In Persian with English summary].
Janeczko A., Tóbiás I., Skoczowski A., Dubert F., Gullner G, Barna B., 2012. Progesterone attenuates both cell membrane damage and loss of photosynthetic efficiency caused by infection with Pseudomonas bacteria in Arabidopsis thaliana. Biologia Plantarum. 56, 192–196
Janeczko, A., 2000. Influence of selected steroids on plant physiological processes especially flowering induction. Ph.D. Thesis, Agriculture University, Krakow.
Janeczko, A., Filek, W., Biesaga-Kościelniak, J., Marcińska, I., Janeczko, Z., 2003. The influence of animal sex hormones on the Iinduction of fowering in Arabidopsis thaliana: comparison with the effect of 24-Epibrassinolide. Plant Cell, Tissue and Organ Culture. 72, 147-151
Janeczko, A., Kocurek, M., Marcińska, I., 2012. Mammalian androgen stimulates photosynthesis in drought-stressed soybean. Central European Journal of Biology. 7, 902-909.
Janeczko, A., Skoczowski, A., 2005. Mammalian sex hormones in plants. Folia Histochemica ET Cytobiologica. 43, 71-79.
Jensen, C.R., Battilani, A., Plauborg, F., Psarras, G., Chartzoulakis, K., Jovanovic, Z. Li, G., Andersen, M.N., 2010. Deficit irrigation based on drought tolerance and root signaling in potatoes and tomatoes. Agricultural Water Management. 98, 403-413.
Jovanovic, Z., Stikic, R., Vucelic-Radovic, B., Paukovic, M., Brocic, Z., Matoric, G., Rovcanin, S., Mojevic, M., 2010. Partial root zone drying increases WUE, N and antioxidant content in field potatoes. European Journal of Agronomy. 33, 124-131.
Khan, H., Link, U., Hocking, W., Stoddard, F., 2007. Evaluation of physiological traits for improving drought tolerance in faba bean (Vicia faba L.). Plant and Soil. 292, 205-217.
Khaninejad, S., Khazaie, H.R., Nabati, J., Kafi, M., 2017. Effect of three species of Mycorrhiza inoculation on yield and some physiological properties of two potato cultivars under drought stress in controlled conditions. Iranian Journal of Field Crops Research. 14, 558-574. [In Persian with English summary].
Liu, F., Shahnazri, A., Andersen, M.N., Jacobsen, S.E., Jensen, C.R., 2006. Effects of deficit irrigation (DI) and partial root drying (PRD) on gas exchange, biomass partitioning and water use efficiency in potato. Scientia Horticulturae. 109, 113-117.
Mac-Adam J. W., Nelson C.J., Sharp R.E., 1992. Peroxidase activity in the leaf elongation zone of tall fescue I. Spatial distribution of ionically bound peroxidase activity in genotypes differing in length of the elongation zone. Plant Physiology, 99, 872-878.
Martre P., Morillon R., Barrieu F., North G.B., Nobel P.S., Chrispeels M.J., 2002. Plasma membrane aquaporins play a significant role during recovery from water deficit. Plant Physiology. 130, 2101–2110.
Masoudi-Sadaghiani, F., Abdollahi- Mandoulakani, B., Zardoshti, M. R., Rasouli-Sadaghiani, M. H. and Tavakoli, A., 2011. Response of proline, soluble sugars, photosynthetic pigments and antioxidant enzymes in potato (Solanum tuberosum L.) to different irrigation regimes in greenhouse condition. Australian Journal of Crop Science. 5, 55-60.
Morillon R., Catterou M., Sangwan R.S., Sangwan B.S., Lassalles J.P., 2001. Brassinolide may control aquaporin activities in Arabidopsis thaliana. Planta. 212, 199-204
Nouri, A., Ahmad Nezami, A., Kafi, M, Hassanpanah. D., 2016. Evaluation of water deficit tolerance of 10 potato cultivars based on some physiological traits and (Solanum tuberosum L.) tuber yield in Ardabil region. Journal of Crop Ecophysiology. 1, 243-268. [In Persian with English summary].
Nozari, E., Asghari-Zakaria, R., Jahanbakhsh, S., Zare, N., 2018. The effect of steroidal testosterone hormone on seedling growth, antioxidant enzymes activity and callus induction in German chamomile (Matricaria chamomilla L.). Journal of Crop Breeding. 10, 31-38. [In Persian with English summary].
Papdi, C.A.,´ Braha´m, E., Joseph, M.P., Popescu, C., Koncz, C., Szabados, L., 2008. Functional identification of Arabidopsis stress regulatory genes using the controlled cDNA overexpression system. Plant Physiology. 147, 528–542.
Raymond J., Rakariyatham, N., Azanza J. L., 1993. Purification and some properties of polyphenoloxidase from sunflower seeds. Phytochemistry. 34, 927–931.
Rykaczewska, K., 2013. The impact of high temperature during growing season on potato cultivars with different response to environmental stresses. American Journal of Plant Sciences. 04, 2386–2393.
Samaee, M., Mohammad Modarres-Sanavy, S. A., Mousapour Gorji. A., Zand, E., 2016. Water use efficiency and water productivity in potato genotypes under water stress conditions. Journal of Water and Soil Conservation. 6, 15-31. [In Persian].
Schultz, M.M., Minarik, T.A., Martinovic-Weigelt, D., Curran, E.M., Bartell, S.E., Schoenfuss, H.L., 2013. Environmental estrogens in an urban aquatic ecosystem: II. Biological effects. Environment International. 61, 138-149.
Shore, L.S., Kapulink, Y., Ben-Dor, B., Fridman, Y., Winninger, S., Shenesh, M., 1992. Effects of estrone and 17-β-estradiol on vegetative growth of Medicago sativa. Plant Physiology. 84, 217-222.
Singh, J., Kaur, L., Mc carthy, O. J., Moughan, P. J., Singh, H., 2009. Development and characterization of extruded snacks from New Zealand taewa (Maori potato) flours. Food Research International. 42, 663-673.
Sriom, S., Mishra, D. P., Rajbhar, P., Singh, D., Singh, R. K., Mishra, S. K., 2017. Effect of different levels of nitrogen on growth and yield in potato (Solanum Tuberosum L.) Cv. Kufri Khyati. International Journal of Current Microbiology and Applied Sciences, 6, 1456–1460.
Steyn, J.M., Kagabo, D.M., Annandale, J.G., 2007.Potato growth and yield responses to irrigation regimes in contrasting seasons a subtropical region. African Crop Science Conference Proceeding. 8, 1647-1651.
Sumpter, J.P. and Jobling, S., 2013. The occurrence, causes and consequences of estrogens in the aquatic environment. Environmental Toxicology and Chemistry, 32, 249-251.
Ylstra, B., Touraev, A., Brinkmann, A.O., Heberle-Bors, E. Tunen, A., 1995. Steroid hormones stimulate germination and tube growth of in vitro matured tobacco pollen. Plant Physiology. 107, 639-643.