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      Integrative roles of nitric oxide and hydrogen sulfide in melatonin‐induced tolerance of pepper ( Capsicum annuum L.) plants to iron deficiency and salt stress alone or in combination

      1 , 2 , 3 , 4 , 4 , 5
      Physiologia Plantarum
      Wiley

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          Abstract

          <p class="first" id="d5840571e117">There seems to be no report in the literature on the effect of melatonin (MT) in relieving the detrimental effects of combined application of salt stress (SS) and iron deficiency (ID). Therefore, the effect of MT on the accumulation/synthesis of endogenous nitric oxide (NO) and hydrogen sulphide (H2 S) and how far these molecules are involved in MT-improved tolerance to the combined application of ID and SS in pepper (Capsicum annuum L) were tested. Hence, two individual trials were set up. The treatments in the first experiment comprised: Control, ID (0.1 mM FeSO4 ), SS (100 mM NaCl) and ID + SS. The detrimental effects of combined stresses were more prominent than those by either of the single stress, with respect to growth, oxidative stress and antioxidant defense attributes. Single stress or both in combination improved the endogenous H2 S and NO, and foliar-applied MT (100 µM) led to a further increase in NO and H2 S levels. In the second experiment, 0.1 mM scavenger of NO, 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide potassium salt (cPTIO) and that of H2 S, hypotuarine (HT) were applied along with MT to get further evidence whether NO and H2 S are involved in MT-induced tolerance to ID and SS. MT combined with cPTIO and HT under a single or combined stress showed that NO effect was reversed by the NO scavenger, cPTIO, alone but the H2 S effect was inhibited by both scavengers. These findings suggested that tolerance to ID and SS induced by MT may be involved in downstream signal crosstalk between NO and H2 S. </p>

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          Most cited references14

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          Identification of melatonin in plants and its effects on plasma melatonin levels and binding to melatonin receptors in vertebrates.

          Twenty-four edible plants were investigated for the presence of melatonin, heretofore considered to be a molecule found only in the animal kingdom. The amount of melatonin in different plants varied greatly with highest melatonin being present in plants of the rice family. Melatonin was identified by radioimmunoassay and verified by high performance liquid chromatography with fluorescence detection. Feeding a diet containing plant products rich in melatonin to chicks increased radioimmunoassayable levels of melatonin in their blood. Likewise, melatonin extracted from plants inhibited binding of [125I]iodomelatonin to rabbit brain. Thus, melatonin ingested in foodstuffs enters the blood and is capable of binding to melatonin binding sites in the brain of mammals.
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            Exogenous Melatonin Confers Salt Stress Tolerance to Watermelon by Improving Photosynthesis and Redox Homeostasis

            Melatonin, a pleiotropic signal molecule, has been shown to play important roles in the regulation of plant growth, development, and responses to environmental stresses. Since a few species have been investigated to unveil the effect of exogenous melatonin on salt stress, the underlying mechanism of melatonin-mediated salt stress tolerance in other plant species still remains largely unknown. In this study, the effects of melatonin on leaf photosynthesis and redox homeostasis in watermelon were examined under salt stress (300 mM NaCl) along with different doses of melatonin (50, 150, and 500 μM) pretreatment. NaCl stress inhibited photosynthesis and increased accumulation of reactive oxygen species and membrane damage in leaves of watermelon seedlings. However, pretreatment with melatonin on roots alleviated NaCl-induced decrease in photosynthetic rate and oxidative stress in a dose-dependent manner. The protection of photosynthesis by melatonin was closely associated with the inhibition of stomatal closure and improved light energy absorption and electron transport in photosystem II, while the reduction of oxidative stress by melatonin was attributed to the improved redox homeostasis coupled with the enhanced activities of antioxidant enzymes. This study unraveled crucial role of melatonin in salt stress mitigation and thus can be implicated in the management of salinity in watermelon cultivation.
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              Alleviation of aluminum toxicity by hydrogen sulfide is related to elevated ATPase, and suppressed aluminum uptake and oxidative stress in barley.

              Greenhouse hydroponic experiments were performed to evaluate potential role of H(2)S on Al toxicity in barley seedlings. Seedlings pretreated with 200 μM NaHS as a donor of H(2)S for 24h and subsequently exposed to 100 μM AlCl(3) for 24h had significantly longer roots than those without NaHS. The promoted root elongation was correlated with a substantial decrease in Al-induced overproduction of lipid peroxidation, electrolyte leakage and Al accumulation in roots, and a marked increase in Al-induced depress activities of Na(+)K(+)-ATPase and H(+)-ATPase. The alleviating role of H(2)S on Al-induced toxicity was also found in a time- and dose-dependent experiment. Addition of 200 and 400 μM NaHS to 100 μM AlCl(3) effectively alleviated Al-toxicity, markedly diminished Al-induced MDA accumulation, and increased chlorophyll content, net photosynthetic rate (Pn) and maximal photochemical efficiency (Fv/Fm) compared with Al alone. Exogenous H(2)S significantly elevated depressed CAT activities, and further improved root POD activity. Moreover, NaHS decreased Al accumulation, but elevated concentrations of S, P, Ca, Mg and Fe in plants. These data suggest that H(2)S-induced alleviation in Al toxicity is attributed to reduced Al uptake and MDA accumulation, improved uptake of P, Ca, Mg and Fe, and elevated ATPase and photosynthetic performance. Copyright © 2012 Elsevier B.V. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Physiologia Plantarum
                Physiol Plantarum
                Wiley
                0031-9317
                1399-3054
                May 07 2019
                May 07 2019
                Affiliations
                [1 ]Soil Science and Plant Nutrition DepartmentHarran University Sanliurfa Turkey
                [2 ]Department of Biological &amp; Environmental SciencesUniversity of Hertfordshire Hatfield AL10 9AB UK
                [3 ]Institute of Molecular Biology and BiotechnologyThe University of Lahore Lahore Pakistan
                [4 ]Botany and Microbiology DepartmentCollege of Science, King Saud University Riyadh Saudi Arabia
                [5 ]Department of BotanyS.P. College Srinagar Jammu and Kashmir India
                Article
                10.1111/ppl.12976
                30980533
                6d41d94d-6b79-48f3-b4a1-c8ae8a3c8a28
                © 2019

                http://doi.wiley.com/10.1002/tdm_license_1.1

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