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      Exogenously applied growth regulators protect the cotton crop from heat-induced injury by modulating plant defense mechanism

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          Abstract

          Episodes of extremely high temperature during reproductive stages of cotton crops are common in many parts of the world. Heat stress negatively influences plant growth, physiology and ultimately lint yield. This study attempts to modulate heat-induced damage to cotton crops via application of growth regulators e.g. hydrogen peroxide (H 2O 2 30ppm), salicylic acid (SA 50ppm), moringa leaf extract (MLE 30 times diluted) and ascorbic acid (ASA 70ppm). Cotton plants were exposed to different thermal regimes by staggering sowing time (field) or exposing to elevated temperatures (38/24 °C and 45/30 °C) for one week during reproductive growth stages (glasshouse). Elevated temperatures significantly induced lipid membrane damage, which was evident from an increased malondialdehyde (MDA) level in cotton leaves. Heat-stressed plants also experienced a significant reduction in leaf chlorophyll contents, net photosynthetic rate and lint yield. Hydrogen peroxide outclassed all the other regulators in increasing leaf SOD, CAT activity, chlorophyll contents, net photosynthetic rate, number of sympodial branches, boll weight and fiber quality components. For example, hydrogen peroxide improved boll weight of heat stressed plants by 32% (supra), 12% (sub) under glasshouse and 18% (supra) under field conditions compared with water treated plants under the same temperatures. Growth regulators, specifically, H 2O 2 protected physiological processes of cotton from heat-induced injury by capturing reactive oxygen species and modulating antioxidant enzymes. Thus, cotton performance in the future warmer climates may be improved through regulation (endogenous) or application (exogenous) hormones during reproductive phases.

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          Most cited references39

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          Production of reactive oxygen intermediates (O(2)(.-), H(2)O(2), and (.)OH) by maize roots and their role in wall loosening and elongation growth.

          Cell extension in the growing zone of plant roots typically takes place with a maximum local growth rate of 50% length increase per hour. The biochemical mechanism of this dramatic growth process is still poorly understood. Here we test the hypothesis that the wall-loosening reaction controlling root elongation is effected by the production of reactive oxygen intermediates, initiated by a NAD(P)H oxidase-catalyzed formation of superoxide radicals (O(2)(.-)) at the plasma membrane and culminating in the generation of polysaccharide-cleaving hydroxyl radicals ((.)OH) by cell wall peroxidase. The following results were obtained using primary roots of maize (Zea mays) seedlings as experimental material. (1) Production of O(2)(.-), H(2)O(2), and (.)OH can be demonstrated in the growing zone using specific histochemical assays and electron paramagnetic resonance spectroscopy. (2) Auxin-induced inhibition of growth is accompanied by a reduction of O(2)(.-) production. (3) Experimental generation of (.)OH in the cell walls with the Fenton reaction causes wall loosening (cell wall creep), specifically in the growing zone. Alternatively, wall loosening can be induced by (.)OH produced by endogenous cell wall peroxidase in the presence of NADH and H(2)O(2). (4) Inhibition of endogenous (.)OH formation by O(2)(.-) or (.)OH scavengers, or inhibitors of NAD(P)H oxidase or peroxidase activity, suppress elongation growth. These results show that juvenile root cells transiently express the ability to generate (.)OH, and to respond to (.)OH by wall loosening, in passing through the growing zone. Moreover, inhibitor studies indicate that (.)OH formation is essential for normal root growth.
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            ROS signalling--specificity is required.

            Reactive oxygen species (ROS) production increases in plants under stress. ROS can damage cellular components, but they can also act in signal transduction to help the cell counteract the oxidative damage in the stressed compartment. H(2)O(2) might induce a general stress response, but it does not have the required specificity to selectively regulate nuclear genes required for dealing with localized stress, e.g. in chloroplasts or mitochondria. Here we argue that peptides deriving from proteolytic breakdown of oxidatively damaged proteins have the requisite specificity to act as secondary ROS messengers and regulate source-specific genes and in this way contribute to retrograde ROS signalling during oxidative stress. Likewise, unmodified peptides deriving from the breakdown of redundant proteins could help coordinate organellar and nuclear gene expression.
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              Thermotolerance and antioxidant systems in Agrostis stolonifera: involvement of salicylic acid, abscisic acid, calcium, hydrogen peroxide, and ethylene.

              This study investigated whether pre-treating plants with specific putative signaling components and heat acclimation would induce tolerance of a cool-season grass, creeping bentgrass (Agrostis stolonifera var. palustris), to subsequent heat stress and whether thermotolerance induction of those pretreatments was associated with the regulation of antioxidant regenerating enzymes. The treatments included foliar application of salicylic acid (SA), abscisic acid (ABA), calcium chloride (CaCl2), hydrogen peroxide (H2O2), 1-aminocyclopropane-1-carboxylic acid (ACC, a precursor of ethylene prior to the exposure of plants to heat stress (35 degrees C) in a growth chamber. Physiological measurements including turf quality, leaf photosynthetic rate, and levels of oxidative damage demonstrated that all treatments increased heat tolerance. The better heat tolerance for pre-treated plants as compared to controls was related to the protection of oxidative damage under heat stress. APX activity increased over the first 2 days and 5 days of heating for ACC and CaCl2 respectively, but for only 12 h for H2O2. SA and ABA pre-treatments had no effects on APX activity earlier, but maintained APX activity at a significantly higher level than in controls after 24 h of heating. SA and ABA pre-treatments had no effects on POX activity. ACC treatment significantly increased POX activity. Pre-treatment with CaCl2, H2O2, and HA reduced POX activity, particularly during the later phase of heating. Plants treated with SA, CaCl2, H2O2 and HA had lower CAT activity than their control plants prior to heating and within 48 h of heat stress. ABA and ACC pre-treatments maintained higher CAT activity than the controls after 48 h of heating. ACC, CaCl2, or HA pre-treatments increased SOD activity only before 5 days of heat stress. SA and ABA pre-treatments had less effect on APX activity earlier under heat stress. These results suggest that specific groups of potential signaling molecules may induce tolerance of creeping bentgrass to heat stress by reducing oxidative damage.
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                Author and article information

                Contributors
                shafaqataligill@yahoo.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                20 November 2018
                20 November 2018
                2018
                : 8
                : 17086
                Affiliations
                [1 ]GRID grid.464523.2, Agronomic Research Institute, , Ayub Agricultural Research Institute, ; Faisalabad, Pakistan
                [2 ]ISNI 0000 0004 0607 1563, GRID grid.413016.1, Department of Agronomy, , University of Agriculture Faisalabad, ; Faisalabad, Pakistan
                [3 ]ISNI 0000 0000 9320 7537, GRID grid.1003.2, Queensland Alliance for Agriculture and Food Innovation, Centre for Plant Science, , The University of Queensland Wilsonton Heights, ; Toowoomba, QLD 4350 Australia
                [4 ]ISNI 0000 0004 0637 891X, GRID grid.411786.d, Department of Environmental Sciences and Engineering, , Government College University Allama Iqbal Road, ; 38000 Faisalabad, Pakistan
                [5 ]ISNI 0000 0004 0607 1563, GRID grid.413016.1, Institute of Soil and Environmental Sciences, , University of Agriculture, ; Faisalabad, 38000 Pakistan
                [6 ]ISNI 0000 0004 1773 5396, GRID grid.56302.32, Department of Botany and Microbiology, , College of Science, King Saud University, ; Riyadh, Saudi Arabia
                [7 ]Department of Botany, S.P. College, Maulana Azad Road, Srinagar, Jammu and Kashmir 190001 India
                Author information
                http://orcid.org/0000-0001-6775-3937
                http://orcid.org/0000-0003-2734-4180
                Article
                35420
                10.1038/s41598-018-35420-5
                6244283
                30459328
                0a47dbca-aed8-47d9-b49b-17a5c8a6ad76
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 8 August 2018
                : 5 November 2018
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