Modulation of plant polyamine and ethylene biosynthesis; and brassinosteroid signaling during Bacillus endophyticus J13-mediated salinity tolerance in Arabidopsis thaliana

IF 4 3区 生物学 Q1 PLANT SCIENCES Journal of plant physiology Pub Date : 2024-06-29 DOI:10.1016/j.jplph.2024.154304
P.T. Nikhil, Umema Faiz, Raunak Sharma, Sridev Mohapatra
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Abstract

Salinity stress adversely impacts plant growth and development. Plant growth-promoting rhizobacteria (PGPR) are known to confer salinity stress tolerance in plants through several mechanisms. Here, we report the role of an abiotic stress-tolerant PGPR strain, Bacillus endophyticus J13, in promoting salinity stress tolerance in Arabidopsis thaliana, by elucidating its impact on physiological responses, polyamine (PA) and ethylene biosynthesis, and brassinosteroid signaling. Physiological analysis revealed that J13 can significantly improve the overall plant growth under salt stress by increasing the biomass, relative water content, and chlorophyll content, decreasing membrane damage and lipid peroxidation, and modulating proline homeostasis in plants. Evaluation of shoot polyamine levels upon J13 inoculation revealed an overall decrease in the levels of the three major PAs, putrescine (Put), spermidine (Spd), and spermine (Spm), under non-stressed conditions. Salt stress significantly increased the levels of Put and Spm, while decreasing the Spd levels in the plants. J13 inoculation under salt-stressed conditions, significantly decreased the Put levels, bringing them closer to those of the untreated control plants, whereas Spd and Spm levels did not change relative to the non-inoculated salt-stressed plants. The modulation of PA levels was accompanied by changes in the expressions of key PA biosynthetic genes under all treatments. Among the ethylene biosynthetic genes that we studied, ACS1 was induced by J13 inoculation under salt stress. J13 inoculation under salt stress resulted in the modulation of the expressions of BR-signaling genes, upregulating the expressions of the positive regulators of BR-signaling (BZR1 and BES2) and downregulating that of the negative regulator (BIN2). Our results provide a new avenue for J13-mediated salt stress amelioration in Arabidopsis, via tight control of polyamine and ethylene biosynthesis and enhanced brassinosteroid signaling.

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拟南芥在内生芽孢杆菌 J13 介导的耐盐性过程中对植物多胺和乙烯生物合成以及铜绿素信号的调节
盐度胁迫对植物的生长和发育有不利影响。众所周知,植物生长促进根瘤菌(PGPR)可通过多种机制赋予植物耐盐碱胁迫的能力。在这里,我们报告了一种耐受非生物胁迫的 PGPR 菌株--内生芽孢杆菌 J13 在促进拟南芥耐盐碱胁迫中的作用,阐明了它对生理反应、多胺(PA)和乙烯生物合成以及类黄铜素信号转导的影响。生理学分析表明,J13能提高植物的生物量、相对含水量和叶绿素含量,减少膜损伤和脂质过氧化反应,调节植物体内的脯氨酸平衡,从而显著改善植物在盐胁迫下的整体生长状况。对接种 J13 后嫩枝多胺水平的评估表明,在非胁迫条件下,三种主要多胺--腐胺(Put)、亚精胺(Spd)和精胺(Spm)的水平总体下降。盐胁迫明显增加了植株中 Put 和 Spm 的含量,同时降低了 Spd 的含量。在盐胁迫条件下接种 J13 能明显降低 Put 的含量,使其接近未处理的对照植株,而 Spd 和 Spm 的含量与未接种的盐胁迫植株相比没有变化。在所有处理下,PA 水平的调节都伴随着关键 PA 生物合成基因表达量的变化。在我们研究的乙烯生物合成基因中,盐胁迫下接种 J13 会诱导 ACS1。在盐胁迫下接种 J13 可调节 BR 信号转导基因的表达,上调 BR 信号转导正调控因子(BZR1 和 BES2)的表达,下调负调控因子(BIN2)的表达。我们的研究结果为 J13 介导的拟南芥盐胁迫改善提供了一条新途径,即通过严格控制多胺和乙烯的生物合成以及增强铜绿素类固醇信号转导。
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来源期刊
Journal of plant physiology
Journal of plant physiology 生物-植物科学
CiteScore
7.20
自引率
4.70%
发文量
196
审稿时长
32 days
期刊介绍: The Journal of Plant Physiology is a broad-spectrum journal that welcomes high-quality submissions in all major areas of plant physiology, including plant biochemistry, functional biotechnology, computational and synthetic plant biology, growth and development, photosynthesis and respiration, transport and translocation, plant-microbe interactions, biotic and abiotic stress. Studies are welcome at all levels of integration ranging from molecules and cells to organisms and their environments and are expected to use state-of-the-art methodologies. Pure gene expression studies are not within the focus of our journal. To be considered for publication, papers must significantly contribute to the mechanistic understanding of physiological processes, and not be merely descriptive, or confirmatory of previous results. We encourage the submission of papers that explore the physiology of non-model as well as accepted model species and those that bridge basic and applied research. For instance, studies on agricultural plants that show new physiological mechanisms to improve agricultural efficiency are welcome. Studies performed under uncontrolled situations (e.g. field conditions) not providing mechanistic insight will not be considered for publication. The Journal of Plant Physiology publishes several types of articles: Original Research Articles, Reviews, Perspectives Articles, and Short Communications. Reviews and Perspectives will be solicited by the Editors; unsolicited reviews are also welcome but only from authors with a strong track record in the field of the review. Original research papers comprise the majority of published contributions.
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