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Acta Physiologiae Plantarum

, 40:203 | Cite as

Protective effect of a natural ally on simultaneous mild heat and salt episodes in maize seedlings

  • Necla PehlivanEmail author
  • Neslihan S. GulerEmail author
Original Article
  • 81 Downloads

Abstract

Abiotic stresses occur together in several combinations in nature and do not usually act alone. However, studies on plants mainly are limited to a single stress type. Yet, atmospheric trends make it indispensable to expand approaches to investigate physiological consequences under multiple abiotic stresses. The potential of Melatonin (Mel) hydropriming on photosynthetic machinery and antioxidant system was investigated in this study. Mel hydropriming (0.1 mmol/mL) resulted in leaf photochemistry protection, which is characterized by maximum photochemical efficiency of PSII, photosynthetic pigments intactness, reactive oxygen species (ROS) scavenging enzymes activation accompanying depressed levels of endogenous hydrogen peroxide (H2O2) and membrane oxidation in maize seedlings at early vegetative stage under combination of 150 mM NaCl and 37 ± 3 °C mild heat. Mimicking nature by combining stresses is more realistic to study abiotic stress responses. High antioxidant capacity of melatonin can serve as a hydropriming substance to withstand simultaneous heat and salt stress.

Keywords

Melatonin Free radical Photosystem Maize Combined stresses 

Notes

Acknowledgements

This work was conducted with the grant provided by the Research Fund of Recep Tayyip Erdogan University (Project ID: 645).

References

  1. Aebi H (1983) Catalase. In: Bergmeyer H (ed) Methods of enzymatic analysis. Weinheim-Verlag Chemie, Weinheim, pp 273–286Google Scholar
  2. Arnao MB, Hernández-Ruiz J (2006) The physiological function of melatonin in plants. Plant Signal Behav 1:89–95PubMedPubMedCentralCrossRefGoogle Scholar
  3. Ashraf M (2010) Inducing drought tolerance in plants: recent advances. Biotechnol Adv 28:169–183PubMedCrossRefGoogle Scholar
  4. Ashraf M, Harris PJC (2013) Photosynthesis under stressful environments: an overview. Photosynthetica 51:163–190CrossRefGoogle Scholar
  5. Beauchamp C, Fridovich I (1971) Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal Biochem 44:276–287PubMedCrossRefGoogle Scholar
  6. Bokszczanin KL, Fragkostefanakis S (2013) Perspectives on deciphering mechanisms underlying plant heat stress response and thermotolerance. Front Plant Sci 4:315PubMedPubMedCentralCrossRefGoogle Scholar
  7. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Anal Biochem 72:248–254PubMedCrossRefGoogle Scholar
  8. Dawood MG, El-Awadi ME (2015) Alleviation of salinity stress on Vicia faba L. plants via seed priming with melatonin. Acta Biol Colomb 20(2):223–235Google Scholar
  9. FAO (Food and Agriculture Organization of the United Nations) (2016) Save and grow in practice maize rice wheat a guide to sustainable cereal production, Rome. http://www.fao.org/3/a i4009e.pdf. Accessed 4 Apr 2018
  10. Foyer CH, Halliwell B (1976) Presence of glutathione and glutathione reductase in chloroplast: a proposed role in ascorbic acid metabolism. Planta 133:21–25PubMedCrossRefGoogle Scholar
  11. Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. I. Kinetics and stoichiometry of fatty acid peroxidation. Arch Biochem Biophys 125:189–198PubMedCrossRefGoogle Scholar
  12. Janas KM, Posmyk MM (2013) Melatonin, an underestimated natural substance with great potential for agricultural application. Acta Physiol Plant 35:3285–3292CrossRefGoogle Scholar
  13. Kataria S, Jajoo A, Guruprasad KN (2014) Impact of increasing ultraviolet-B (UV-B) radiation on photosynthetic processes. J Photochem Photobiol B 137:55–66PubMedCrossRefGoogle Scholar
  14. Kolodziejczyk I, Dzitko K, Szewcyk R, Posmyk MM (2016) Exogenous melatonin improves corn (Zea mays L.) embryo proteome in seeds subjected to chilling stress. J Plant Physiol 193:47–56PubMedCrossRefGoogle Scholar
  15. Lack B, Daya S, Nyokong T (2001) Interaction of serotonin and melatonin with sodium, potassium, calcium, lithium and aluminium. J Pineal Res 31:102–108PubMedCrossRefGoogle Scholar
  16. Li W, Zhang C, Lu Q, Wen X, Lu C (2011) The combined effect of salt stress and heat shock on proteome profiling in Suaeda salsa. J Plant Physiol 168:1743–1752PubMedCrossRefGoogle Scholar
  17. Li X, Wei JP, Scott ER et al (2018) Exogenous melatonin alleviates cold stress by promoting antioxidant defense and redox homeostasis in Camellia sinensis L. Molecules 23:165PubMedCentralCrossRefGoogle Scholar
  18. Liang D, Gao F, Ni Z, Lin Z, Deng Q, Tang Y et al (2018) Melatonin improves heat tolerance in kiwifruit seedlings through promoting antioxidant enzymatic activity and glutathione s-transferase transcription. Molecules 6:23Google Scholar
  19. Martinez V, Nieves-Cordones M, Lopez-Delacalle M et al (2018) Tolerance to stress combination in tomato plants: new insights in the protective role of melatonin. Molecules 23:535PubMedCentralCrossRefGoogle Scholar
  20. Nar H, Saglam A, Terzi R, Várkonyi Z, Kadioglu A (2009) Leaf rolling and photosystem II efficiency in Ctenanthe setosa exposed to drought stress. Photosynthetica 47:429–436CrossRefGoogle Scholar
  21. Pandey P, Ramegowda V, Senthil-Kumar M (2015) Shared and unique responses of plants to multiple individual stresses and stress combinations: physiological and molecular mechanisms. Front Plant Sci 36:6e14Google Scholar
  22. Paredes DS, Reiter RJ (2010) Melatonin: Helping cells cope with oxidative disaster. Cell Membr Free Radic Res 2:99–108Google Scholar
  23. Porra RJ, Thompson WA, Kriendemann PE (1989) Determination of accurate extinction coefficients and simultaneous equations for assaying chlorophyll a and b extracted with four different solvents: verification of the concentration of chlorophyll standards by atomic absorption spectroscopy. Biochim Biophys Acta 975:384–394CrossRefGoogle Scholar
  24. Reiter RJ, Tan DX, Galano A (2014) Melatonin reduces lipid peroxidation and membrane viscosity. Front Physiol 5:1–4CrossRefGoogle Scholar
  25. Rivero RM, Mestre TC, Mittler R, Rubio F, Garcia-Sanchez F, Martinez V (2014) The combined effect of salinity and heat reveals a specific physiological, biochemical and molecular response in tomato plants. Plant Cell Environ 37:1059–1073PubMedCrossRefGoogle Scholar
  26. Rukavtsova EB, Lebedeva AA, Zakharchenko NS, Buryanov YI (2013) The ways to produce biologically safe marker-free transgenic plants. Russ J Plant Physiol 60:14–26CrossRefGoogle Scholar
  27. Saraswat S, Yadav AK, Sirohi P, Singh NK (2017) Role of epigenetics in crop improvement: water and heat stress. J Plant Biol 60:231–240CrossRefGoogle Scholar
  28. Shi H, Jiang C, Ye T, Tan DX et al (2015) Comparative physiological, metabolomic, and transcriptomic analyses reveal mechanisms of improved abiotic stress resistance in bermudagrass [Cynodon dactylon (L). Pers.] by exogenous melatonin. J Exp Bot 66:681–694PubMedCrossRefGoogle Scholar
  29. Urbanek H, Kuzniak-Gebarowska E, Herka K (1991) Elicitation of defense responses in bean leaves by Botrytis cinerea polygalacturonase. Acta Physiol Plant 13:43–50Google Scholar
  30. 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 Sci 151:59–66CrossRefGoogle Scholar
  31. Wang P, Sun X, Li C, Wei Z, Liang D, Ma F (2013a) Long-term exogenous application of melatonin delays drought-induced leaf senescence in apple. J Pineal Res 54:292–302PubMedCrossRefGoogle Scholar
  32. Zhang J, Li H, Xu B, Li J, Huang B (2016) Exogenous melatonin suppresses dark-induced leaf senescence by activating the superoxide dismutase-catalase antioxidant pathway and down-regulating chlorophyll degradation in excised leaves of perennial ryegrass (Lolium perenne L.). Front Plant Sci 7:1500PubMedPubMedCentralGoogle Scholar
  33. Zhang YP, Yang SJ, Chen YY (2017) Effects of melatonin on photosynthetic performance and antioxidants in melon during cold and recovery. Biol Plant 61:571–578CrossRefGoogle Scholar
  34. Zheng XD, Tan DX, Allan AC, Zuo BX, Zhao Y, Reiter RJ, Wang L, Wang Z, Guo Y, Zhou JZ, Shan DQ, Li QT, Han ZH, Kong J (2017) Chloroplastic biosynthesis of melatonin and its involvement in protection of plants from salt stress. Sci Rep 7:41236PubMedPubMedCentralCrossRefGoogle Scholar

Copyright information

© Franciszek Górski Institute of Plant Physiology, Polish Academy of Sciences, Kraków 2018

Authors and Affiliations

  1. 1.Department of Biology, Faculty of Arts and SciencesRecep Tayyip Erdogan UniversityRizeTurkey
  2. 2.Department of Nutrition and Dietetics, Faculty of Health SciencesKaradeniz Technical UniversityTrabzonTurkey

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