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      Eustress with H 2O 2 Facilitates Plant Growth by Improving Tolerance to Salt Stress in Two Wheat Cultivars

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          Abstract

          In this study, the positive role of hydrogen peroxide (H 2O 2) pretreatment in mitigating the adverse impacts of seawater stress has been evaluated in two wheat ( Triticum aestivum L.) cultivars, namely Gemmiza 11 as a salt-sensitive and Misr 1 as a salt-tolerant cultivar, with contrasting phenotypes in response to the salinity stress. Under normal conditions, wheat seeds eustress with H 2O 2 have shown significant effects on the improvement of plant growth parameters, such as dry weight and root and shoot lengths. Under salt stress conditions, seeds eustress with H 2O 2 have shown a reduction in damage to plant growth and physiological parameters as compared to the seeds kept as un-primed in both wheat cultivars. In addition, eustress of seeds with H 2O 2 has induced an increment in the pigments content, proline level and mineral uptake (K +, Ca 2+ and Mg 2+). Moreover, seeds eustress with H 2O 2 have shown significant decrement in Na + content uptake in plants and that subsequently reduced lipid peroxidation. Seawater stress has increased the activity of the antioxidant system based on catalase (CAT), peroxidase (POD) and ascorbate peroxidase (APX) in both cultivars, except POD in Gemmiza 11. Similarly, the application of H 2O 2 has further enhanced the activity of the antioxidant system in stressed plants and this enhancement of the antioxidant system further reduced Na + content in plants and subsequently increased the growth parameters. Results of inter-simple sequence repeat (ISSR) markers have shown clear differentiation among the treatments and have provided strong evidence in support of the hypothesis proposed in this study that H 2O 2 eustress improves seed tolerance and enhances plant growth parameters under seawater stress.

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          Rapid determination of free proline for water-stress studies

          Plant and Soil, 39(1), 205-207
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            Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants.

            Despite the recognition of H(2)O(2) as a central signaling molecule in stress and wounding responses, pathogen defense, and regulation of cell cycle and cell death, little is known about how the H(2)O(2) signal is perceived and transduced in plant cells. We report here that H(2)O(2) is a potent activator of mitogen-activated protein kinases (MAPKs) in Arabidopsis leaf cells. Using epitope tagging and a protoplast transient expression assay, we show that H(2)O(2) can activate a specific Arabidopsis mitogen-activated protein kinase kinase kinase, ANP1, which initiates a phosphorylation cascade involving two stress MAPKs, AtMPK3 and AtMPK6. Constitutively active ANP1 mimics the H(2)O(2) effect and initiates the MAPK cascade that induces specific stress-responsive genes, but it blocks the action of auxin, a plant mitogen and growth hormone. The latter observation provides a molecular link between oxidative stress and auxin signal transduction. Finally, we show that transgenic tobacco plants that express a constitutively active tobacco ANP1 orthologue, NPK1, display enhanced tolerance to multiple environmental stress conditions without activating previously described drought, cold, and abscisic acid signaling pathways. Thus, manipulation of key regulators of an oxidative stress signaling pathway, such as ANP1/NPK1, provides a strategy for engineering multiple stress tolerance that may greatly benefit agriculture.
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              Regulation and function of ascorbate peroxidase isoenzymes.

              Even under optimal conditions, many metabolic processes, including the chloroplastic, mitochondrial, and plasma membrane-linked electron transport systems of higher plants, produce active oxygen species (AOS). Furthermore, the imposition of biotic and abiotic stress conditions can give rise to excess concentrations of AOS, resulting in oxidative damage at the cellular level. Therefore, antioxidants and antioxidant enzymes function to interrupt the cascades of uncontrolled oxidation in each organelle. Ascorbate peroxidase (APX) exists as isoenzymes and plays an important role in the metabolism of H(2)O(2) in higher plants. APX is also found in eukaryotic algae. The characterization of APX isoenzymes and the sequence analysis of their clones have led to a number of investigations that have yielded interesting and novel information on these enzymes. Interestingly, APX isoenzymes of chloroplasts in higher plants are encoded by only one gene, and their mRNAs are generated by alternative splicing of the gene's two 3'-terminal exons. Manipulation of the expression of the enzymes involved in the AOS-scavenging systems by gene-transfer technology has provided a powerful tool for increasing the present understanding of the potential of the defence network against oxidative damage caused by environmental stresses. Transgenic plants expressing E. coli catalase to chloroplasts with increased tolerance to oxidative stress indicate that AOS-scavenging enzymes, especially chloroplastic APX isoenzymes are sensitive under oxidative stress conditions. It is clear that a high level of endogenous ascorbate is essential effectively to maintain the antioxidant system that protects plants from oxidative damage due to biotic and abiotic stresses.
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                Author and article information

                Journal
                Plants (Basel)
                Plants (Basel)
                plants
                Plants
                MDPI
                2223-7747
                27 August 2019
                September 2019
                : 8
                : 9
                : 303
                Affiliations
                [1 ]Botany and Microbiology Department, Faculty of Science, South Valley University, 83523 Qena, Egypt
                [2 ]Biology Department, Turabah University College, Taif University, Turabah Branch, 21955 Taif, Saudi Arabia
                [3 ]Department of Plant Biotechnology, Faculty of Agricultural Sciences, University of Guilan, P.O. Box 41635-1314 Rasht, Iran
                [4 ]Rice Research Institute of Iran, Agricultural Research, Education and Extension Organization (AREEO), P.O. Box 41996-13475 Rasht, Iran
                [5 ]Department of Environmental Sciences, COMSATS University Islamabad, Vehari-Campus, Vehari 61100, Pakistan
                [6 ]National Products Department, National Centre for Radiation Research and Technology (NCRRT), Egyptian Atomic Energy Authority, Nasr City, 11787 Cairo, Egypt
                Author notes
                [* ]Correspondence: arafat.moawad@ 123456sci.svu.edu.eg or moawad76@ 123456gmail.com or a.moawd@ 123456tu.edu.sa ; Tel.: +20-11-4132-3284 or +966-50-162-8042
                Author information
                https://orcid.org/0000-0001-5244-4832
                https://orcid.org/0000-0003-0314-1354
                https://orcid.org/0000-0002-1655-2657
                https://orcid.org/0000-0003-0191-1431
                Article
                plants-08-00303
                10.3390/plants8090303
                6783893
                31461870
                eacd6021-f32a-43da-aabd-4956f52974fc
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 16 July 2019
                : 19 August 2019
                Categories
                Article

                antioxidant enzymes,h2o2,inter-simple sequence repeat (issr),eustress,seawater,wheat

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