PlantStress&Biodiversity Lab, Linking Landscape, Environment, Agriculture and Food (LEAF), Instituto Superior de Agronomia (ISA), Universidade de Lisboa, Tapada da Ajuda, 1349-017 Lisbon, Portugal.
Plant Biochemistry Lab, Instituto de Tecnologia Química e Biológica, Universidade NOVA de Lisboa, Av. República, Quinta do Marquês, 2780-157 Oeiras, Portugal.
Int J Mol Sci. 2019 Dec 20;21(1):78. doi: 10.3390/ijms21010078.
displays high levels of salt tolerance, but very little is known about how this tree adapts to saline conditions. To understand the molecular basis of C. glauca response to salt stress, we have analyzed the proteome from branchlets of plants nodulated by nitrogen-fixing Frankia Thr bacteria (NOD) and non-nodulated plants supplied with KNO (KNO), exposed to 0, 200, 400, and 600 mM NaCl. Proteins were identified by Short Gel, Long Gradient Liquid Chromatography coupled to Tandem Mass Spectrometry and quantified by Sequential Window Acquisition of All Theoretical Mass Spectra -Mass Spectrometry. 600 proteins were identified and 357 quantified. Differentially Expressed Proteins (DEPs) were multifunctional and mainly involved in Carbohydrate Metabolism, Cellular Processes, and Environmental Information Processing. The number of DEPs increased gradually with stress severity: (i) from 7 (200 mM NaCl) to 40 (600 mM NaCl) in KNO; and (ii) from 6 (200 mM NaCl) to 23 (600 mM NaCl) in NOD. Protein-protein interaction analysis identified different interacting proteins involved in general metabolic pathways as well as in the biosynthesis of secondary metabolites with different response networks related to salt stress. Salt tolerance in is related to a moderate impact on the photosynthetic machinery (one of the first and most important stress targets) as well as to an enhancement of the antioxidant status that maintains cellular homeostasis.
表现出很高的耐盐性,但对于这种树如何适应盐渍条件知之甚少。为了了解 C. glauca 对盐胁迫的分子基础,我们分析了固氮弗兰克氏菌 Thr 细菌(NOD)接种和非接种植物枝条的蛋白质组,这些植物用 KNO(KNO)供应,并暴露于 0、200、400 和 600 mM NaCl 下。通过短凝胶、长梯度液相色谱与串联质谱联用和顺序窗口采集所有理论质谱 - 质谱定量法鉴定蛋白质。鉴定了 600 种蛋白质,定量了 357 种蛋白质。差异表达蛋白(DEPs)具有多功能性,主要参与碳水化合物代谢、细胞过程和环境信息处理。随着胁迫严重程度的增加,DEPs 的数量逐渐增加:(i)在 KNO 中从 7(200 mM NaCl)增加到 40(600 mM NaCl);(ii)在 NOD 中从 6(200 mM NaCl)增加到 23(600 mM NaCl)。蛋白质-蛋白质相互作用分析确定了不同的相互作用蛋白,它们参与一般代谢途径以及次生代谢物的生物合成,具有不同的与盐胁迫相关的反应网络。对盐的耐受性与对光合作用机制(最早和最重要的应激靶标之一)的适度影响有关,以及抗氧化状态的增强,从而维持细胞内稳态。