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      Drought Tolerance of Soybean ( Glycine max L. Merr.) by Improved Photosynthetic Characteristics and an Efficient Antioxidant Enzyme Activities Under a Split-Root System

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          Abstract

          Water deficiency significantly affects photosynthetic characteristics. However, there is little information about variations in antioxidant enzyme activities and photosynthetic characteristics of soybean under imbalanced water deficit conditions (WDC). We therefore investigated the changes in photosynthetic and chlorophyll fluorescence characteristics, total soluble protein, Rubisco activity (RA), and enzymatic activities of two soybean varieties subjected to four different types of imbalanced WDC under a split-root system. The results indicated that the response of both cultivars was significant for all the measured parameters and the degree of response differed between cultivars under imbalanced WDC. The maximum values of enzymatic activities (SOD, CAT, GR, APX, and POD), chlorophyll fluorescence (Fv/Fm, qP, ɸPSII, and ETR), proline, RA, and total soluble protein were obtained with a drought-tolerant cultivar (ND-12). Among imbalanced WDC, the enhanced net photosynthesis, transpiration, and stomatal conductance rates in T2 allowed the production of higher total soluble protein after 5 days of stress, which compensated for the negative effects of imbalanced WDC. Treatment T4 exhibited greater potential for proline accumulation than treatment T1 at 0, 1, 3, and 5 days after treatment, thus showing the severity of the water stress conditions. In addition, the chlorophyll fluorescence values of FvFm, ɸPSII, qP, and ETR decreased as the imbalanced WDC increased, with lower values noted under treatment T4. Soybean plants grown in imbalanced WDC (T2, T3, and T4) exhibited signs of oxidative stress such as decreased chlorophyll content. Nevertheless, soybean plants developed their antioxidative defense-mechanisms, including the accelerated activities of these enzymes. Comparatively, the leaves of soybean plants in T2 displayed lower antioxidative enzymes activities than the leaves of T4 plants showing that soybean plants experienced less WDC in T2 compared to in T4. We therefore suggest that appropriate soybean cultivars and T2 treatments could mitigate abiotic stresses under imbalanced WDC, especially in intercropping.

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          Rapid determination of free proline for water-stress studies

          Plant and Soil, 39(1), 205-207
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            Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells.

            Drought is a major threat to agricultural production. Plants synthesize the hormone abscisic acid (ABA) in response to drought, triggering a signalling cascade in guard cells that results in stomatal closure, thus reducing water loss. ABA triggers an increase in cytosolic calcium in guard cells ([Ca2+]cyt) that has been proposed to include Ca2+ influx across the plasma membrane. However, direct recordings of Ca2+ currents have been limited and the upstream activation mechanisms of plasma membrane Ca2+ channels remain unknown. Here we report activation of Ca2+-permeable channels in the plasma membrane of Arabidopsis guard cells by hydrogen peroxide. The H2O2-activated Ca2+ channels mediate both influx of Ca2+ in protoplasts and increases in [Ca2+]cyt in intact guard cells. ABA induces the production of H2O2 in guard cells. If H2O2 production is blocked, ABA-induced closure of stomata is inhibited. Moreover, activation of Ca2+ channels by H2O2 and ABA- and H2O2-induced stomatal closing are disrupted in the recessive ABA-insensitive mutant gca2. These data indicate that ABA-induced H2O2 production and the H2O2-activated Ca2+ channels are important mechanisms for ABA-induced stomatal closing.
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              Roles of enzymatic and nonenzymatic antioxidants in plants during abiotic stress.

              Reactive oxygen species (ROS) are produced in plants as byproducts during many metabolic reactions, such as photosynthesis and respiration. Oxidative stress occurs when there is a serious imbalance between the production of ROS and antioxidant defense. Generation of ROS causes rapid cell damage by triggering a chain reaction. Cells have evolved an elaborate system of enzymatic and nonenzymatic antioxidants which help to scavenge these indigenously generated ROS. Various enzymes involved in ROS-scavenging have been manipulated, over expressed or downregulated to add to the present knowledge and understanding the role of the antioxidant systems. The present article reviews the manipulation of enzymatic and nonenzymatic antioxidants in plants to enhance the environmental stress tolerance and also throws light on ROS and redox signaling, calcium signaling, and ABA signaling.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                03 July 2019
                2019
                : 10
                : 786
                Affiliations
                [1] 1Key Laboratory of Crop Ecophysiology and Farming System in Southwest, Ministry of Agriculture, College of Agronomy, Sichuan Agricultural University , Chengdu, China
                [2] 2Department of Agronomy, College of Agriculture, University of Sargodha , Sargodha, Pakistan
                [3] 3Department of Plant Physiology, Slovak University of Agriculture , Nitra, Slovakia
                [4] 4Department of Botany and Plant Physiology, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Science Prague , Prague, Czechia
                [5] 5Institute of Ecological Agriculture, Sichuan Agricultural University , Chengdu, China
                Author notes

                Edited by: Ankush Prasad, Palacký University Olomouc, Czechia

                Reviewed by: Rakesh Kumar Sinha, Biology Centre (ASCR), Czechia; Parvaiz Ahmad, Sri Pratap College Srinagar, India

                *Correspondence: Wenyu Yang, mssiyangwy@ 123456sicau.edu.cn

                These authors have contributed equally to this work

                This article was submitted to Oxidant Physiology, a section of the journal Frontiers in Physiology

                Article
                10.3389/fphys.2019.00786
                6621490
                31333479
                99d51743-8bae-4b10-81ed-6debb7672946
                Copyright © 2019 Iqbal, Hussain, Raza, Yang, Safdar, Brestic, Aziz, Hayyat, Asghar, Wang, Zhang, Yang and Liu.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 07 February 2019
                : 04 June 2019
                Page count
                Figures: 6, Tables: 0, Equations: 0, References: 56, Pages: 13, Words: 7690
                Funding
                Funded by: National Key Research and Development Program of China 10.13039/501100012166
                Award ID: 2016YFD0300209
                Funded by: China Agriculture Research System
                Award ID: CARS-04-PS19
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 31301277
                Categories
                Physiology
                Original Research

                Anatomy & Physiology
                enzymatic activity,chlorophyll fluorescence,polyethylene glycol,reactive oxygen species,rubisco activity

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