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Exogenously applied glycinebetaine induced alteration in some key physio-biochemical attributes and plant anatomical features in water stressed oat (Avena sativa L.) plants

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Abstract

Although exogenous application of glycinebetaine (GB) is widely reported to regulate a myriad of physio-biochemical attributes in plants under stressful environments including drought stress, there is little information available in the literature on how and up to what extent GB can induce changes in anatomical features in water starved plants. Thus, the present research work was conducted to assess the GB-induced changes in growth, physio-biochemical, and anatomical characteristics in two cultivars (CK-1 and F-411) of oat (Avena sativa L.) under limited water supply. After exposure to water stress, a considerable reduction was observed in plant growth in terms of lengths and weights of shoot and roots, leaf mesophyll thickness, leaf midrib thickness, root cortex thickness, root diameter, stem diameter, stem phloem area, and stem vascular bundle area in both oat cultivars. However, water stress resulted in a significant increase in leaf total phenolics, hydrogen peroxide (H2O2), ascorbic acid (AsA), GB contents, activities of enzymes (CAT, SOD and POD), total soluble proteins, leaf epidermis (abaxial and adaxial) thickness, bulliform cell area, sclerenchyma thickness, root endodermis and epidermis thickness, root metaxylem area, stem metaxylem area and stem sclerenchyma thickness in both oat cultivars. Foliar-applied 100 mM GB suppressed H2O2 contents, while improved growth attributes, free proline and GB contents, activity of SOD enzyme, leaf abaxial epidermis thickness, leaf bulliform cell area, leaf midrib thickness, leaf sclerenchyma thickness, root cortex thickness, root endodermis, epidermis thickness, root stele diameter, stem diameter, stem epidermis thickness, stem metaxylem area, and stem phloem and vascular bundle area in both oat cultivars. For both oat cultivars, CK-1 was superior to F-411 in leaf abaxial epidermis thickness, leaf mesophyll, leaf sclerenchyma, root metaxylem area, stem diameter, stem epidermis, sclerenchyma thickness, stem metaxylem area, and stem vascular bundle area. Overall, both oat cultivars showed inconsistent behavior to water stress and foliar-applied GB in terms of different physio-biochemical attributes, however, CK-1 was superior to F-411 in a number of anatomical features of leaf, root, and stem.

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References

  • Abdel C G, Al-Rawi I M T. 2011. Anatomical alteration in response to irrigation and water stress in some legume crops. American Journal of Experimental Agriculture, 1(4): 231–264.

    Article  Google Scholar 

  • Ahmad P, Rasool S, Gul A, et al. 2016. Jasmonates: Multifunctional roles in stress tolerance. Frontiers in Plant Science, 7: 813.

    Google Scholar 

  • Ahmed M F E M, Mac D M, Bashir A A G. 2011. Effect of water stress at different periods on seed yield and water use efficiency of guar under Shambat conditions. Agricultural Sciences, 2(3): 262–266.

    Article  Google Scholar 

  • Akram N A, Shahbaz M, Ashraf M. 2007. Relationship of photosynthetic capacity and proline accumulation with the growth of differently adapted populations of two potential grasses (Cynodon dactylon (L.) Pers. and Cenchrus ciliaris L.) to drought stress. Pakistan Journal of Botany, 39(3): 777–786.

    Google Scholar 

  • Akram N A, Noreen S, Noreen T, et al. 2015. Exogenous application of trehalose alters growth, physiology and nutrient composition in radish (Raphanus sativus L.) plants under water deficit conditions. Brazilian Journal of Botany, 38(3): 431–439.

    Article  Google Scholar 

  • Akram N A, Shafiq S, Ashraf M, et al. 2016. Drought-induced anatomical changes in radish (Raphanus sativus L.) leaves supplied with trehalose through different modes. Arid Land Research and Management, 30(4): 412–420.

    Article  Google Scholar 

  • Aldesuquy H S, Abbas M A, Abo-Hamed S A, et al. 2013. Does glycine betaine and salicylic acid ameliorate the negative effect of drought on wheat by regulating osmotic adjustment through solutes accumulation? Journal of Stress Physiology and Biochemistry, 9(3): 5–22.

    Google Scholar 

  • Arnon D I. 1949. Copper enzymes in isolated chloroplast, polyphenoloxidase in Beta vulgaris L. Journal of Plant Physiology, 24(1): 1–15.

    Article  Google Scholar 

  • Ashikari M, Feng-Ma J. 2015. Exploring the power of plants to overcome environmental stresses. Rice (NY), 8: 10.

    Article  Google Scholar 

  • Ashraf M, Foolad M R. 2007. Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany, 59(2): 206–216.

    Article  Google Scholar 

  • Ashraf M, Athar H R, Harris P J C, et al. 2008. Some prospective strategies for improving crop salt tolerance. Advances in Agronomy, 97: 45–110.

    Article  Google Scholar 

  • Ashraf M. 2010. Inducing drought tolerance in plants: recent advances. Biotechnology Advances, 28(1): 169–183.

    Article  Google Scholar 

  • Ashraf M, Akram N A, Al-Qurainy F, et al. 2011. Drought tolerance: Roles of organic osmolytes, growth regulators, and mineral nutrients. Advances in Agronomy, 111: 249–296.

    Article  Google Scholar 

  • Ashraf M, Harris P J C. 2013. Photosynthesis under stressful environments: An overview. Photosynthetica, 51(2): 163–190.

    Article  Google Scholar 

  • Balsamo R A, Willigen C V, Baue A M, et al. 2006. Drought tolerance of selected Eragrostis species correlates with leaf tensile properties. Annals of Botany, 97(6): 985–991.

    Article  Google Scholar 

  • Bates L S, Waldren R P, Teare I D. 1973. Rapid determination of free proline for water stress studies. Plant and Soil, 39(1): 205–207.

    Article  Google Scholar 

  • Behnamnia M, Kalantari K M, Rezanejad F. 2009. Exogenous application of brassinosteroid alleviates drought-induced oxidative stress in Lycopersicon esculentum L. General and Applied Plant Physiology, 35(1–2): 22–34.

    Google Scholar 

  • Bloch D, Hoffmann C M, Märander B. 2006. Impact of water supply on photosynthesis, water use and carbon isotope discrimination of sugar beet genotypes. European Journal of Agronomy, 24(3): 218–225.

    Article  Google Scholar 

  • Boughalleb F, Abdellaoui R, Brahim N, et al. 2014. Anatomical adaptations of Astragalus gombiformis Pomel. under drought stress. Central European Journal of Biology, 9(12): 1215–1225.

    Google Scholar 

  • Bradford M M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Annual Biochemistry, 72(1–2): 248–254.

    Article  Google Scholar 

  • Carmak I, Horst W J. 1991. Effects of aluminum on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max). Physiologia Plantarum, 83(3): 463–468.

    Article  Google Scholar 

  • Chance B, Maehly A C. 1955. Assay of catalases and peroxidases. Methods in Enzymology, 2: 764–775.

    Article  Google Scholar 

  • Cha-um S, Kirdmanee C. 2010. Effect of glycinebetaine on proline, water use, and photosynthetic efficiencies, and growth of rice seedlings under salt stress. Turkish Journal of Agriculture and Forestry, 34: 517–527.

    Google Scholar 

  • Chaves M M, Oliveira M M. 2004. Mechanisms underlying plant resilience to water deficits: Prospects for water-saving agriculture. Journal of Experimental Botany, 55(407): 2365–2384.

    Article  Google Scholar 

  • Chen T H H, Murata N. 2008. Glycinebetaine: an effective protectant against abiotic stress in plants. Trends in Plant Science, 13(9): 499–505.

    Article  Google Scholar 

  • Farooq M, Basra S M A, Wahid A, et al. 2008. Physiological role of exogenously applied glycinebetaine to improve drought tolerance in fine grain aromatic rice (Oryza sativa L.). Journal of Agronomy and Crop Sciences, 194(5): 325–333.

    Article  Google Scholar 

  • Ghorbanli M, Gafarabad M, Amirkian T, et al. 2013. Investigation of proline, total protein, chlorophyll, ascorbate and dehydroascorbate changes under drought stress in Akria and Mobil tomato cultivars. Iranian Journal of Plant Physiology, 3(2): 651–658.

    Google Scholar 

  • Giannopolitis C N, Ries S K. 1977. Superoxide dismutase. I. Occurrence in higher plants. Plant Physiology, 59(2): 309–314.

    Article  Google Scholar 

  • Giri J. 2011. Glycinebetaine and biotic stress tolerance in plants. Plant Signaling & Behavior, 6(11): 1746–1751.

    Article  Google Scholar 

  • Grieve C M, Grattan S R. 1983. Rapid assay for determination of water soluble quaternary ammonium compounds. Plant and Soil, 70(2): 303–307.

    Article  Google Scholar 

  • Hameed A, Goher M, Iqbal N. 2013. Drought induced programmed cell death and associated changes in antioxidants, proteases, and lipid peroxidation in wheat leaves. Biologia Plantarum, 57(2): 370–374.

    Article  Google Scholar 

  • Hamidou F, Zombre G, Diouf O, et al. 2007. Physiological, biochemical and agro-morphological responses of five cowpea genotypes (Vigna unguiculata (L.) Walp.) to water deficit under glasshouse conditions. Biotechnology, Agronomie, Societie and Environment, 11(3): 225–234.

    Google Scholar 

  • Hasheminasab H, Assad M T, Aliakbari A, et al. 2012. Influence of drought stress on oxidative damage and antioxidant defense systems in tolerant and susceptible wheat genotypes. Journal of Agricultural Science, 4(8): 20–30.

    Article  Google Scholar 

  • Hossain M A, Fujita M. 2010. Evidence for a role of exogenous glycinebetaine and proline in antioxidant defense and methylglyoxal detoxification systems in mung bean seedlings under salt stress. Physiology and Molecular Biology of Plants, 16(1): 19–29.

    Article  Google Scholar 

  • Hussain M, Malik M A, Farooq M, et al. 2008. Improving drought tolerance by exogenous application of glycinebetaine and salicylic acid in sunflower. Journal of Agronomy and Crop Science 194(3): 193–199.

    Article  Google Scholar 

  • Iqbal N, Ashraf M, Ashraf M Y. 2009. Influence of exogenous glycine betaine on gas exchange and biomass production in sunflower (Helianthus annuus L.) under water limited conditions. Journal of Agronomy and Crop Science, 195(6): 420–426.

    Article  Google Scholar 

  • Jatoi W A, Baloch M J, Kumbhar M B, et al. 2011. Effect of water stress on physiological and yield parameters at anthesis stage in elite spring wheat cultivars. Sarhad Journal of Agriculture, 27: 59–65.

    Google Scholar 

  • Julkunen-Tiitto R. 1985. Phenolic constituents in the leaves of north willows: methods for the analysis of certain phenolics. Journal of Agricultural and Food Chemistry, 33(2): 213–217.

    Article  Google Scholar 

  • Khan M A, Shirazi M U, Khan M A, et al. 2009. Role of proline, K/Na ratio and chlorophyll content in salt tolerance of wheat (Triticum aestivum L.). Pakistan Journal of Botany, 41(2): 633–638.

    Google Scholar 

  • Kumar R R, Karajol K, Naik G R. 2011. Effect of polyethylene glycol induced water stress on physiological and biochemical responses in pigeon pea (Cajanus cajan L. Mill sp.). Recent Research in Science & Technology, 3: 148–152.

    Google Scholar 

  • Lum M S, Hanafi M M, Rafii Y M, et al. 2014. Effect of drought stress on growth, proline and antioxidant enzyme activities of upland rice. Journal of Animal and Plant Sciences, 24(5): 1487–1493.

    Google Scholar 

  • Ma Q Q, Wang W, Li Y H, et al. 2006. Alleviation of photoinhibition in drought-stressed wheat (Triticum aestivum L.) by foliar-applied glycinebetaine. Journal of Plant Physiology, 163(2): 165–175.

    Article  Google Scholar 

  • Ma X L, Wang Y J, Xie S L, et al. 2007. Glycinebetaine application ameliorates negative effects of drought stress in tobacco. Russian Journal of Plant Physiology, 54: 472–479.

    Article  Google Scholar 

  • Mafakheri A, Siosemardeh A, Bahramnejad B, et al. 2010. Effect of drought stress on yield, proline and chlorophyll contents in three chickpea cultivars. Australian Journal of Crop Science, 4(8): 580–585.

    Google Scholar 

  • Mahmood T, Ashraf M, Shahbaz M. 2009. Does exogenous application of glycinebetaine as a pre-sowing seed treatment improve growth and regulate some key physiological attributes in wheat plants grown under water deficit conditions? Pakistan Journal of Botany, 41(3): 1291–1302.

    Google Scholar 

  • Makbul S, Coskuncelebi K, Turkmen Z, et al. 2006. Morphology and anatomy of Scrophularia L. (Scrophulariaceae) taxa from NE anatolia. Acta Biologica Cracoviensia Series Botanica, 48(1): 33–43.

    Google Scholar 

  • Makbul S, Türkmen Z, Coskuncelebi K, et al. 2008. Anatomical and pollen characters in the genus Epilobium L. (Onagraceae) from northeast anatolia. Acta Biologica Cracoviensia Series Botanica, 50(1): 51–62.

    Google Scholar 

  • Makbul S, Guler N S, Durmus N, et al. 2011. Changes in anatomical and physiological parameters of soybean under drought stress. Turkish Journal of Botany, 35: 369–377.

    Google Scholar 

  • Mukherjee S P, Chouduri M A. 1983. Implications of water stress induced changes in the levels of endogenous ascorbic acid and hydrogen peroxide in Vigna seedlings. Physiologia Plantarum, 58(2): 166–170.

    Article  Google Scholar 

  • Mwenye O J, van Rensburg L, van Biljon A, et al. 2016. The role of proline and root traits on selection for drought-stress tolerance in soybeans: A review. South African Journal of Plant and Soil, 33(4): 245–256.

    Article  Google Scholar 

  • Nawaz K, Ashraf M. 2010. Exogenous application of glycinebetaine modulates activities of antioxidants in maize plants subjected to salt stress. Journal of Agronomy and Crop Science, 196(1): 28–37.

    Article  Google Scholar 

  • Nawaz T, Hameed M, Ashraf M, et al. 2013. Modifications in root and stem anatomy for water conservation in some diverse blue panic (Panicum antidotale Retz.) ecotypes under drought stress. Arid Land Research and Management, 27(3): 286–297.

    Article  Google Scholar 

  • Nemeskéri E, Sárdi É, Remenyik J, et al. 2010. Study of the defensive mechanism against drought in French bean (Phaseolus vulgaris L.) varieties. Acta Physiologia Plantarum, 32(6): 1125–1134.

    Article  Google Scholar 

  • Omar A A. 2012. Impact of drought stress on germination and seedling growth parameters of some wheat cultivars. Life Science Journal, 9(1): 590–598.

    Google Scholar 

  • Ozorgucu B, Gemici Y, Turkan I. 1991. Comparative Plant Anatomy. İzmir: Ege University Faculty of Science Publication No: 129. (in Turkish)

    Google Scholar 

  • Pratap V, Sharma Y K. 2010. Impact of osmotic stress on seed germination and seedling growth in black gram (Phaseolus mungo). Journal of Environmental Biology, 31(5): 721–726.

    Google Scholar 

  • Raza M A S, Saleem M F, Khan I H, et al. 2012. Evaluating the drought stress tolerance efficiency of wheat (Triticum aestivum L.) cultivars. Russian Journal of Agricultural and Socio-Economic Science, 12(12): 41–46.

    Google Scholar 

  • Rezaei M A, Kaviani B, Masouleh A K. 2012. The effect of exogenous glycine betaine on yield of soybean (Glycine max (L.) Merr.) in two contrasting cultivars Pershing and DPX under soil salinity stress. Plant Omics Journal, 5(2): 87–93.

    Google Scholar 

  • Ruzin S E. 1999. Plant Microtechnique and Microscopy. New York: Oxford University Press, 322.

    Google Scholar 

  • Sadiq M, Akram N A, Ashraf M. 2017. Foliar applications of alpha-tocopherol improve the composition of fresh pods of Vigna radiata subjected to water deficiency. Turkish Journal of Botany, 41: 244–252.

    Article  Google Scholar 

  • Saeed N, Maqbool N, Haseeb M, et al. 2016. Morpho-anatomical changes in roots of chickpea (Cicer arietinum L.) under drought stress condition. Journal of Agricultural Science and Technology, 6: 1–9.

    Google Scholar 

  • Seki M, Kamei A, Yamaguchi-Shinozaki K, et al. 2003. Molecular responses to drought, salinity and frost: common and different paths for plant protection. Current Opinion in Biotechnology, 14(2): 194–199.

    Article  Google Scholar 

  • Shafiq S, Akram N A, Ashraf M. 2015. Does exogenously-applied trehalose alter oxidative defense system in the edible part of radish (Raphanus sativus L.) under water-deficit conditions? Scientia Horticulturae, 185: 68–75.

    Article  Google Scholar 

  • Shahbaz M, Masood Y, Ashraf M. 2011. Is foliar-applied glycinebetaine effective in mitigating the adverse effects of drought stress on wheat (Triticum aestivum L.)? Journal of Applied Botany and Food Quality, 84(2): 192–199.

    Google Scholar 

  • Snedecor G W, Cochran W G. 1980. Statistical Methods (7th ed.). Ames: Iowa State University Press, 97.

    Google Scholar 

  • Subbarao G V, Wheeler R M, Levine L H, et al. 2001. Glycine betaine accumulation, ionic and water relations of red-beet at contrasting levels of sodium supply. Journal of Plant Physiology, 158(6): 767–776.

    Article  Google Scholar 

  • Vasellati V, Oesterheld M, Medan D, et al. 2001. Effects of flooding and drought on the anatomy of Paspalum dilatatum. Annals of Botany, 88(3): 355–360.

    Article  Google Scholar 

  • Velikova V, Yordanov I, Edreva A. 2000. Oxidative stress and some antioxidant systems in acid rain-treated bean plants: Protective role of exogenous polyamines. Plant Science, 151(1): 59–66.

    Article  Google Scholar 

  • Wang W, Vinocur B, Altman A. 2003. Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance. Planta, 218(1): 1–14.

    Article  Google Scholar 

  • Zhang L, Gao M, Hu J, et al. 2012. Modulation role of abscisic acid (ABA) on growth, water relations and glycinebetaine metabolism in two maize (Zea mays L.) cultivars under drought stress. International Journal of Molecular Sciences, 13: 3189–3202.

    Article  Google Scholar 

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Acknowledgments

The research work presented in this manuscript was financially supported by the Department of Botany, Government College University, Faisalabad, Pakistan.

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Shehzadi, A., Akram, N.A., Ali, A. et al. Exogenously applied glycinebetaine induced alteration in some key physio-biochemical attributes and plant anatomical features in water stressed oat (Avena sativa L.) plants. J. Arid Land 11, 292–305 (2019). https://doi.org/10.1007/s40333-019-0007-8

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