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      Drought and Salinity Stresses Response in Three Korean Native Herbaceous Plants and Their Suitability as Garden Plants

      , , , , ,
      Horticulturae
      MDPI AG

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          Abstract

          Native garden plants significantly contribute to the conservation of biodiversity and ecosystem functions in urban environments. This study aimed to identify the physiochemical differences among native herbaceous plants subjected to drought or salinity stress and to assess their potential as garden plants adaptable to outdoor conditions and global climate change. Physiological parameters, such as chlorophyll (SD; −86.7% and −61.5%, SS: −85% and −76.5%) and carotenoid (SD; −84.5% and −58.3%, SS; −80.5% and −76%), decreased in Melica grandiflora and Carex forficula in severe drought or salinity treatment. In contrast, Carex boottiana maintained high water-use efficiency (SD: +97.5%, SS: +262.9%) under severe drought or salinity conditions, with no significant changes observed in chlorophyll (SD: +9.5%, SS: −3.7%) or carotenoid levels (SD: +35.2%, SS: +0.3%) compared to the WW or UT conditions. Biochemical analyses indicated that C. boottiana exhibited lower or slightly higher levels of malondialdehyde in SS (−22.5%) and reactive oxygen species such as O2− (SD: +9.9%; SS: −9.4%) than those observed in the other species under severe stress conditions. Principal component analysis revealed clear differences in tolerance levels among the native species. C. boottiana demonstrated high adaptability to both drought and salinity stress, indicating its potential as a sustainable and resilient garden material for urban landscapes facing severe climatic challenges.

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          Mechanisms of salinity tolerance.

          The physiological and molecular mechanisms of tolerance to osmotic and ionic components of salinity stress are reviewed at the cellular, organ, and whole-plant level. Plant growth responds to salinity in two phases: a rapid, osmotic phase that inhibits growth of young leaves, and a slower, ionic phase that accelerates senescence of mature leaves. Plant adaptations to salinity are of three distinct types: osmotic stress tolerance, Na(+) or Cl() exclusion, and the tolerance of tissue to accumulated Na(+) or Cl(). Our understanding of the role of the HKT gene family in Na(+) exclusion from leaves is increasing, as is the understanding of the molecular bases for many other transport processes at the cellular level. However, we have a limited molecular understanding of the overall control of Na(+) accumulation and of osmotic stress tolerance at the whole-plant level. Molecular genetics and functional genomics provide a new opportunity to synthesize molecular and physiological knowledge to improve the salinity tolerance of plants relevant to food production and environmental sustainability.
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            Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants.

            Various abiotic stresses lead to the overproduction of reactive oxygen species (ROS) in plants which are highly reactive and toxic and cause damage to proteins, lipids, carbohydrates and DNA which ultimately results in oxidative stress. The ROS comprises both free radical (O(2)(-), superoxide radicals; OH, hydroxyl radical; HO(2), perhydroxy radical and RO, alkoxy radicals) and non-radical (molecular) forms (H(2)O(2), hydrogen peroxide and (1)O(2), singlet oxygen). In chloroplasts, photosystem I and II (PSI and PSII) are the major sites for the production of (1)O(2) and O(2)(-). In mitochondria, complex I, ubiquinone and complex III of electron transport chain (ETC) are the major sites for the generation of O(2)(-). The antioxidant defense machinery protects plants against oxidative stress damages. Plants possess very efficient enzymatic (superoxide dismutase, SOD; catalase, CAT; ascorbate peroxidase, APX; glutathione reductase, GR; monodehydroascorbate reductase, MDHAR; dehydroascorbate reductase, DHAR; glutathione peroxidase, GPX; guaicol peroxidase, GOPX and glutathione-S- transferase, GST) and non-enzymatic (ascorbic acid, ASH; glutathione, GSH; phenolic compounds, alkaloids, non-protein amino acids and α-tocopherols) antioxidant defense systems which work in concert to control the cascades of uncontrolled oxidation and protect plant cells from oxidative damage by scavenging of ROS. ROS also influence the expression of a number of genes and therefore control the many processes like growth, cell cycle, programmed cell death (PCD), abiotic stress responses, pathogen defense, systemic signaling and development. In this review, we describe the biochemistry of ROS and their production sites, and ROS scavenging antioxidant defense machinery. Copyright © 2010 Elsevier Masson SAS. All rights reserved.
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              COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS

              D ARNON (1949)

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                Contributors
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                Journal
                HORTCF
                Horticulturae
                Horticulturae
                MDPI AG
                2311-7524
                November 2024
                November 19 2024
                : 10
                : 11
                : 1225
                Article
                10.3390/horticulturae10111225
                2ac5e92a-955a-495d-937a-8debe508d93d
                © 2024

                https://creativecommons.org/licenses/by/4.0/

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