一个功能性的光呼吸循环对拟南芥表皮依赖光的气孔打开至关重要。

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Azhin Mortezazadeh, Michael Hodges, Mathieu Jossier
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引用次数: 0

摘要

传统上认为光呼吸是一种浪费的途径,但它在细胞代谢和应激反应中起着重要作用。虽然其在叶肉细胞中的作用已被明确,但其在叶表皮保护细胞中的功能及其与气孔打开的关系尚不清楚。通过数据挖掘,所有的光呼吸基因都得到了表达,并且它们各自的蛋白都存在于拟南芥保护细胞中,从而表明存在一个完整的光呼吸循环。羟吡啶-甲烷-磺酸(HPMS)或氨基乙酸-腈(AAN)对甘氨酸脱羧酶复合物(GDC)的抑制作用降低了拟南芥叶片表皮表皮的气孔开度。丝氨酸、3-磷酸甘油酸或苹果酸的外源供应减轻了这种抑制作用。因此,保护细胞的光呼吸代谢通过支持对保护细胞膨胀调节至关重要的代谢物通量来促进光诱导的气孔打开。这些发现强调了气孔动力学中功能性保护细胞光呼吸循环的重要性,它可能在植物对环境刺激的反应中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Functional Photorespiratory Cycle Is Essential for Light-Dependent Stomata Opening in Epidermal Peels of Arabidopsis thaliana.

Traditionally viewed as a wasteful pathway, photorespiration plays essential roles in cellular metabolism and stress responses. While its role in leaf mesophyll cells is well characterized, its functioning in leaf epidermal guard cells and its involvement in stomatal opening remain poorly understood. Using data mining, all photorespiratory genes were expressed, and their respective proteins were present in Arabidopsis thaliana guard cells, thus indicating the presence of a complete photorespiratory cycle. The inhibition of glycolate oxidase (GOX) by hydroxy-pyridyl-methane-sulfonic acid (HPMS) or the glycine decarboxylase complex (GDC) by amino-aceto-nitrile (AAN) reduced light-induced stomatal opening in Arabidopsis thaliana leaf epidermal peels. The exogenous supply of serine, 3-phosphoglycerate, or malate alleviated this inhibition. It is proposed that guard cell photorespiratory metabolism contributes to light-induced stomatal opening by supporting metabolite fluxes crucial for the regulation of guard cell turgor. These findings highlight the importance of a functional guard cell photorespiratory cycle in stomatal dynamics that could play a role in plant responses to environmental stimuli.

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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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