在大气CO2浓度升高的情况下,缓生根瘤菌和固氮螺旋菌共接种可减轻大豆内涝的有害影响

IF 5.7 2区 生物学 Q1 PLANT SCIENCES
Eduardo Pereira Shimoia , Douglas Antônio Posso , Cristiane Jovelina da-Silva , Adriano Udich Bester , Nathalia Dalla Corte Bernardi , Junior Borella , Ivan Ricardo Carvalho , Ana Claudia Barneche de Oliveira , Luis Antonio de Avila , Luciano do Amarante
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引用次数: 0

摘要

大气中二氧化碳浓度的上升直接影响C3植物的光合作用和生产力,导致全球变暖和水文循环的改变,进而增加极端降雨事件。大豆是一种对涝渍敏感的作物,在这种条件下产量明显下降。豆科植物与重氮营养菌建立共生关系,并越来越多地与植物生长促进菌(PGPB)共接种,以增强逆境适应能力。虽然升高的CO2 (e[CO2])和PGPB通常会刺激光合作用和生长,但内涝常常通过增强光呼吸活动抵消这些益处。研究了在涝渍和e[CO2] (750 μmol mol−1 vs环境420 μmol mol−1)条件下,接种慢生根瘤菌(IB)和共接种巴西偶氮螺旋菌(CA)对大豆碳氮代谢的影响。在V4期,植物经历了7天的涝渍,然后4天的排水。测量包括气体交换、乙醇酸氧化酶(GO)、谷氨酰胺合成酶(GS)、谷氨酸合成酶(GOGAT)和生物特征。e[CO2]显著增强了气体交换,CA进一步放大了这一效应。e[CO2]和CA之间的协同作用提高了胁迫和恢复期间的光合性能。在CA和e[CO2]作用下,氧化石墨烯活性降低,但在涝渍作用下,氧化石墨烯活性短暂升高。涝渍上调GS-GOGAT活性,排水后GS-GOGAT活性恢复到基线水平。在e[CO2]处理下,GS-GOGAT活性下降,但CA保持比IB更高的活性。共接种植株在所有条件下都改善了生长指标,e[CO2]进一步提高了性能。总的来说,e[CO2]改善了光合作用,抑制了光呼吸,而CA减轻了涝渍诱导的光呼吸应激,并保持了氮代谢。这些结果表明,共接种固氮螺旋菌和e[CO2]可协同提高大豆的抗涝能力,为气候智慧型农业提供可持续战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-inoculation of Bradyrhizobium and Azospirillum mitigates the deleterious effects of waterlogging in soybean plants in a scenario of enhanced atmospheric CO2
Rising atmospheric CO2 concentrations directly influence photosynthesis and productivity in C3 plants, contributing to global warming and altering hydrological cycles, which in turn increase extreme rainfall events. Soybean, a waterlogging-sensitive crop, exhibits marked yield reductions under such conditions. Legumes establish symbioses with diazotrophic bacteria and are increasingly co-inoculated with plant growth-promoting bacteria (PGPB) to enhance stress resilience. While elevated CO2 (e[CO2]) and PGPB generally stimulate photosynthesis and growth, waterlogging often counteracts these benefits by intensifying photorespiratory activity. This study investigated the effects of Bradyrhizobium inoculation (IB) and co-inoculation with Azospirillum brasilense (CA) on soybean carbon and nitrogen metabolism under waterlogging and e[CO2] (750 μmol mol−1 vs. ambient 420 μmol mol−1). At the V4 stage, plants were subjected to seven days of waterlogging followed by four days of drainage. Measurements included gas exchange, glycolate oxidase (GO), glutamine synthetase (GS), glutamate synthase (GOGAT), and biometric traits. e[CO2] significantly enhanced gas exchange, an effect further amplified by CA. The synergistic interaction between e[CO2] and CA improved photosynthetic performance during both stress and recovery. GO activity was reduced under CA and e[CO2], though it increased transiently under waterlogging. Waterlogging upregulated GS-GOGAT activity, which returned to baseline after the post-drainage. Under e[CO2], GS-GOGAT activity declined, but CA maintained higher activity than IB. Co-inoculated plants improved the growth metrics under all conditions, with e[CO2] further enhancing performance. Overall, e[CO2] improved photosynthesis and suppressed photorespiration, while CA mitigated waterlogging-induced photorespiratory stress and preserved nitrogen metabolism. These results demonstrate that co-inoculation with Azospirillum and e[CO2] synergistically enhances soybean resilience to waterlogging, offering a sustainable strategy for climate-smart agriculture.
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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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