Fe3O4-NPs 和肠杆菌在缓解小麦(Triticum aestivum L.)汞胁迫方面的协同效应:形态-生理-生化属性的启示

IF 6.1 2区 生物学 Q1 PLANT SCIENCES
Wenhan Dong
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A pot experiment was conducted over 60 days using wheat (<em>Triticum aestivum</em> L.) to investigate the effects of varying Hg levels (0, 50 and 100 mg kg<sup>⎯1</sup>) combined with different concentrations of Fe<sub>3</sub>O<sub>4</sub>–NPs (25 and 50 mg L<sup>-1</sup>) and <em>E. cloacae</em> (10 and 20 ppm) on various morpho−physio−biochemical responses. The research outcomes indicated that elevated levels of Hg stress in the soil significantly (<em>P</em> &lt; 0.05) decreased plant growth and biomass, photosynthetic pigments, nutrients uptake and gas exchange attributes. However, Hg stress also induced oxidative stress in the plants by increasing malondialdehyde (MDA) and hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), which also induced increased compounds of various enzymatic and non-enzymatic antioxidants and also the gene expression and sugar content. 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Synergistic effects of Fe3O4–NPs and Enterobacter cloacae in alleviating mercury stress in wheat (Triticum aestivum L.): Insights into morpho–physio–biochemicals attributes

Synergistic effects of Fe3O4–NPs and Enterobacter cloacae in alleviating mercury stress in wheat (Triticum aestivum L.): Insights into morpho–physio–biochemicals attributes
In the current industrial scenario, mercury (Hg) as a metal is of great importance but poses a major threat to the ecosystem because of its toxicity, but fewer studies have been conducted on its effects and alleviation strategies by using nanoparticles (NPs) and plant growth promoting rhizobacteria (PGPR). Taking into consideration the positive effects of iron oxide (Fe3O4)⎯NPs and Enterobacter cloacae rhizobacteria in reducing Hg toxicity in plants, the present study was conducted. A pot experiment was conducted over 60 days using wheat (Triticum aestivum L.) to investigate the effects of varying Hg levels (0, 50 and 100 mg kg⎯1) combined with different concentrations of Fe3O4–NPs (25 and 50 mg L-1) and E. cloacae (10 and 20 ppm) on various morpho−physio−biochemical responses. The research outcomes indicated that elevated levels of Hg stress in the soil significantly (P < 0.05) decreased plant growth and biomass, photosynthetic pigments, nutrients uptake and gas exchange attributes. However, Hg stress also induced oxidative stress in the plants by increasing malondialdehyde (MDA) and hydrogen peroxide (H2O2), which also induced increased compounds of various enzymatic and non-enzymatic antioxidants and also the gene expression and sugar content. Furthermore, a significant (P < 0.05) increase in proline metabolism, the ascorbate-glutathione (AsA–GSH) cycle were observed. Although, the application of Fe3O4–NPs and E. cloacae showed a significant (P < 0.05) increase in plant growth and biomass, nutrients uptake, gas exchange characteristics, enzymatic and non-enzymatic compounds, and their gene expression and also decreased oxidative stress. In addition, the application of Fe3O4–NPs and E. cloacae enhanced cellular fractionation and decreased the proline metabolism and AsA–GSH cycle in T. aestivum seedlings. Research findings, therefore, suggest that the application of Fe3O4–NPs and E. cloacae can ameliorate Hg toxicity in T. aestivum seedlings, resulting in improved plant growth and composition under metal stress, as depicted by balanced antioxidant defense mechanism.
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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
期刊介绍: Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement. Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB. Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.
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