耐盐芽孢杆菌 RA 株协调肌醇代谢,赋予番茄耐盐性。

IF 9.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Integrative Plant Biology Pub Date : 2024-07-05 DOI:10.1111/jipb.13733
Fenghui Wu, Zengting Chen, Xiaotong Xu, Xin Xue, Yanling Zhang, Na Sui
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引用次数: 0

摘要

土壤盐碱化是威胁作物产量的世界性问题。一些植物生长促进根瘤菌(PGPR)可以在高盐环境中存活,并帮助植物适应胁迫。然而,这些细菌的基因组和代谢特征以及促进植物耐盐性的调控机制在很大程度上仍然未知。在目前的研究中,一种新型耐盐 PGPR 菌株--芽孢杆菌菌株 RA 能增强番茄对盐胁迫的耐受性。菌株 RA 与其近缘种的基因组比较分析表明,菌株特异性基因表现出高度的进化可塑性,纯化选择驱动的进化限制促进了其基因组对盐分影响土壤的适应。转录组进一步表明,RA菌株可以通过重新规划生物合成途径来平衡能量代谢,从而耐受盐胁迫。植物会释放出大量代谢物,这些代谢物会对植物的适应性产生重大影响。在盐胁迫条件下,叶片中肌醇的积累被观察到,从而促进了由芽孢杆菌 RA 菌株引发的植物生长。重要的是,肌醇在植物叶球微生物组的组装和有益植物物种的招募中起着选择性作用。它能促进植物圈细菌共生网络的不稳定性,但不能促进真菌网络的不稳定性。此外,肌醇还能加强细菌和真菌之间的域间相互作用,以应对盐胁迫。这项研究强调了 RA 对盐分影响土壤的遗传适应性,以及 RA 通过调节肌醇代谢物影响叶球微生物的能力,从而赋予番茄持久的抗盐胁迫能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Halotolerant Bacillus sp. strain RA coordinates myo-inositol metabolism to confer salt tolerance to tomato

Soil salinity is a worldwide problem threatening crop yields. Some plant growth-promoting rhizobacteria (PGPR) could survive in high salt environment and assist plant adaptation to stress. Nevertheless, the genomic and metabolic features, as well as the regulatory mechanisms promoting salt tolerance in plants by these bacteria remain largely unknown. In the current work, a novel halotolerant PGPR strain, namely, Bacillus sp. strain RA can enhance tomato tolerance to salt stress. Comparative genomic analysis of strain RA with its closely related species indicated a high level of evolutionary plasticity exhibited by strain-specific genes and evolutionary constraints driven by purifying selection, which facilitated its genomic adaptation to salt-affected soils. The transcriptome further showed that strain RA could tolerate salt stress by balancing energy metabolism via the reprogramming of biosynthetic pathways. Plants exude a plethora of metabolites that can strongly influence plant fitness. The accumulation of myo-inositol in leaves under salt stress was observed, leading to the promotion of plant growth triggered by Bacillus sp. strain RA. Importantly, myo-inositol serves as a selective force in the assembly of the phyllosphere microbiome and the recruitment of plant-beneficial species. It promotes destabilizing properties in phyllosphere bacterial co-occurrence networks, but not in fungal networks. Furthermore, interdomain interactions between bacteria and fungi were strengthened by myo-inositol in response to salt stress. This work highlights the genetic adaptation of RA to salt-affected soils and its ability to impact phyllosphere microorganisms through the adjustment of myo-inositol metabolites, thereby imparting enduring resistance against salt stress in tomato.

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来源期刊
Journal of Integrative Plant Biology
Journal of Integrative Plant Biology 生物-生化与分子生物学
CiteScore
18.00
自引率
5.30%
发文量
220
审稿时长
3 months
期刊介绍: Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.
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