Co-exposure impact of nickel oxide nanomaterials and Bacillus subtilis on soybean growth and nitrogen assimilation dynamics.

IF 6.9 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2024-12-23 DOI:10.1093/plphys/kiae638
Kashif Khan, Zhen Wei Li, Rayyan Khan, Shahid Ali, Haseeb Ahmad, Muhammad Ali Shah, Xun Bo Zhou
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Abstract

Nickel oxide nanoparticles (NiO-NPs) pose potential threats to agricultural production. Bacillus subtilis has emerged as a stress-mitigating microbe that alleviates the phytotoxicity caused by NiO-NPs. However, the mechanisms underlying its effectiveness, particularly in root-nodule symbiosis and biological N2-fixation (BNF), remain unclear. Here, we tested the combined exposure of NiO-NPs (50 mg kg-1) and B. subtilis on soybean (Glycine max L.) growth and BNF. Combined exposure increased root length, shoot length, root biomass, and shoot biomass by 19% to 26%, while Ni (200 mg kg-1) reduced them by 38% to 53% compared to the control. NiO-NPs at 100 and 200 mg kg-1 significantly (P < 0.05) reduced nodule formation by 16% and 58% and Nitrogen assimilation enzyme activities levels (urease, nitrate reductase, glutamine synthetase, and glutamate synthetase) by 13% to 57%. However, co-exposure with B. subtilis improved nodule formation by 22% to 44%. Co-exposure of NiO-NPs (200 mg kg-1) with B. subtilis increased peroxidase, catalase, and glutathione peroxidase activity levels by 20%, 16%, and 14% while reducing malondialdehyde (14%) and hydrogen peroxide (12%) levels compared to NiO-NPs alone. Additionally, co-exposure of NiO-NPs (100 and 200 mg kg-1) with B. subtilis enhanced the relative abundance of Stenotrophomonas, Gemmatimonas, and B. subtilis, is associated with N2-cycling and N2-fixation potential. This study confirms that B. subtilis effectively mitigates NiO-NP toxicity in soybean, offering a sustainable method to enhance BNF and crop growth and contribute to addressing global food insecurity.

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氧化镍纳米材料与枯草芽孢杆菌共暴露对大豆生长和氮同化动力学的影响
纳米氧化镍(NiO-NPs)对农业生产构成潜在威胁。枯草芽孢杆菌(Bacillus subtilis)已成为一种压力缓解微生物,可减轻NiO-NPs造成的植物毒性。然而,枯草芽孢杆菌的作用机制,尤其是在根-节共生和生物固氮(BNF)方面的作用机制仍不清楚。在此,我们测试了 NiO-NPs(50 mg kg-1)和枯草芽孢杆菌的联合接触对大豆(Glycine max L.)生长和生物固氮的影响。与对照相比,联合接触可使根长、芽长、根生物量和芽生物量增加 19-26%,而 Ni(200 mg kg-1)则使其减少 38-53%。100 和 200 毫克/千克的 NiO-NPs 能显著(P < 0.05)减少 16% 和 58% 的结核形成和 13-57% 的氮同化酶活性水平(UE、NR、HS 和 GOGAT)。然而,与枯草芽孢杆菌共同暴露可使结核形成提高 22-44%。与单独施用 NiO-NPs 相比,与枯草芽孢杆菌共同施用 NiO-NPs(200 毫克/千克)可提高 POD、CAT 和 GSH-Px 活性水平 20%、16% 和 14%,同时降低 MDA(14%)和 H₂O₂ (12%)水平。此外,NiO-NPs(100 和 200 毫克/千克-1)与枯草芽孢杆菌的共同暴露提高了 Stenotrophomonas、Gemmatimonas 和枯草芽孢杆菌的相对丰度,这与 N2 循环和 N2 固定潜力有关。这项研究证实,枯草芽孢杆菌能有效减轻大豆中的NiO-NP毒性,为提高BNF和作物生长提供了一种可持续的方法,有助于解决全球粮食不安全问题。
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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
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