离子稳态、碳水化合物代谢和氧化平衡是野生大豆抗低钾胁迫的基础。

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Mingxia Li, Sunchen Pan, Nuobing Li, Lihui Zhang, Guangye Wang, Yinan Ding, Tian Luan, Yongjun Hu
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引用次数: 0

摘要

农田土壤钾资源的短缺对全球粮食安全构成了重大挑战。野生大豆(Glycine soja)是一种与栽培大豆相关的珍贵野生种质,具有较高的抗逆性和适应性。本研究从生长参数、光合生理、矿质离子及代谢物含量、基因表达等方面对两种野生大豆生态型进行综合比较,旨在阐明野生大豆幼苗叶片抗低钾胁迫的调控机制。结果表明,在耐瘠瘠性野生大豆(GS2)中,与钾离子运输相关的基因显著上调。这促进钾的吸收和运输,保持较高的K+浓度和K+/Na+比。碳水化合物合成在GS2中增强,蔗糖和棉子糖积累增加,三羧酸(TCA)循环更活跃。GS2还能增强抗坏血酸-谷胱甘肽(ASA-GSH)循环,促进水杨酸和4-氨基丁酸GABA合成,增强抗氧化能力和清除活性氧(ROS),维持氧化平衡。在低钾胁迫下,GS2积累不饱和脂肪酸,增强细胞膜流动性,提供抗应力结构屏障。本研究为优质野生大豆资源开发和低钾胁迫抗性基因探索提供了基础,有助于提高栽培大豆对缺钾土壤的适应性,保障全球粮食生产稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ionic Homeostasis, Carbohydrate Metabolism, and Oxidative Balance Underlie Wild Soybean Resistance to Low Potassium Stress.

The scarcity of potassium resources in farmland soils poses a major challenge to global food security. Wild soybean (Glycine soja), a valuable wild germplasm related to cultivated soybeans, is known for its high-stress resistance and adaptability. This study comprehensively compares two wild soybean ecotypes in terms of growth parameters, photosynthetic physiology, mineral ions and metabolite contents, and gene expression, aiming to clarify the regulatory mechanisms of low potassium stress tolerance in wild soybean seedlings' leaves. Results show that in barren-tolerant wild soybean (GS2), genes involved in potassium ion transport were significantly upregulated. This promotes potassium absorption and transport, maintaining a high K+ concentration and K+/Na+ ratio. Carbohydrate synthesis is enhanced in GS2, with increased sucrose and raffinose accumulation and a more active tricarboxylic acid (TCA) cycle. GS2 also strengthens the ascorbic acid-glutathione (ASA-GSH) cycle, along with promoting salicylic acid and 4-aminobutyric acid GABA synthesis, which boosts antioxidant capacity and reactive oxygen species (ROS) scavenging, maintaining oxidative balance. Under low potassium stress, GS2 accumulates unsaturated fatty acids, enhancing cell-membrane fluidity and providing a stress-resistant structural barrier. Overall, this study provides a basis for developing high-quality wild soybean resources and exploring genes for low potassium stress tolerance, which could contribute to improving cultivated soybeans' adaptability to potassium-deficient soils and ensuring global food production stability.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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