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NO3−/H+ Antiport in the Tonoplast of Cucumber Root Cells Is Stimulated by Nitrate Supply: Evidence for a Reversible Nitrate-Induced Phosphorylation of Vacuolar NO3−/H+ Antiport

机译:3号硝酸盐供应刺激黄瓜根细胞液泡膜中的-/ H +反向转运:硝酸盐诱导的空泡NO3磷酸化的证据。-/ H +反端口

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摘要

Studies in the last few years have shed light on the process of nitrate accumulation within plant cells, achieving molecular identification and partial characterization of the genes and proteins involved in this process. However, contrary to the plasma membrane-localized nitrate transport activities, the kinetics of active nitrate influx into the vacuole and its adaptation to external nitrate availability remain poorly understood. In this work, we have investigated the activity and regulation of the tonoplast-localized H+/NO3 antiport in cucumber roots in response to N starvation and NO3 induction. The time course of nitrate availability strongly influenced H+/NO3 antiport activity at the tonoplast of root cells. However, under N starvation active nitrate accumulation within the vacuole still occurred. Hence, either a constitutive H+-coupled transport system specific for nitrate operates at the tonoplast, or nitrate uses another transport protein of broader specificity to different anions to enter the vacuole via a proton-dependent process. H+/NO3 antiport in cucumber was significantly stimulated in NO3 -induced plants that were supplied with nitrate for 24 hours following 6-day-long N starvation. The cytosolic fraction isolated from the roots of NO3 -induced plants significantly stimulated H+/NO3 antiport in tonoplast membranes isolated from cucumbers growing on nitrate. The stimulatory effect of the cytosolic fraction was completely abolished by EGTA and the protein kinase inhibitor staurosporine and slightly enhanced by the phosphatase inhibitors okadaic acid and cantharidin. Hence, we conclude that stimulation of H+/NO3 antiport at the tonoplast of cucumber roots in response to nitrate provision may occur through the phosphorylation of a membrane antiporter involving Ca-dependent, staurosporine-sensitive protein kinase.
机译:最近几年的研究揭示了植物细胞内硝酸盐积累的过程,实现了对该过程中涉及的基因和蛋白质的分子鉴定和部分表征。但是,与质膜局部硝酸盐转运活性相反,活性硝酸盐流入液泡的动力学及其对外部硝酸盐有效性的适应性仍然知之甚少。在这项工作中,我们研究了黄瓜根中液泡膜定位的H + / NO3 -反向转运对N饥饿和NO3 -的活性和调控归纳。硝酸盐有效性的时间过程强烈影响根细胞液泡膜中H + / NO3 -的反转运活性。然而,在氮饥饿下,液泡内仍发生活性硝酸盐积累。因此,要么专门用于硝酸盐的组成型H + 偶联转运系统在液泡膜中运行,要么硝酸盐使用另一种对不同阴离子具有更广泛特异性的转运蛋白通过质子依赖过程进入液泡。 NO 3 -诱导的植株在6天后的24小时内被补充了硝酸盐,可显着刺激黄瓜中H + / NO3 -的反向转运。 -长N饥饿。从NO3 -诱导植物的根中分离出的胞质级分显着刺激了黄瓜生长的液泡膜中的H + / NO3 -反向转运。硝酸盐EGTA和蛋白激酶抑制剂星形孢菌素完全消除了胞质部分的刺激作用,而磷酸酶抑制剂冈田酸和邻苯二酚则略微增强了胞浆部分的刺激作用。因此,我们得出结论,硝酸盐对黄瓜根部液泡膜上H + / NO3 -反向转运的刺激可能是通过涉及Ca-的膜反向转运蛋白的磷酸化而发生的。依赖的星形孢菌素敏感性蛋白激酶。

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