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对马唐(Digitaria sanguinalis)叶肉细胞原生质体胞质pH的流式细胞术分析。

Flow cytometric analysis of cytosolic pH of mesophyll cell protoplasts from the crabgrass Digitaria sanguinalis.

作者信息

Giglioli-Guivarc'h N, Pierre J N, Vidal J, Brown S

机构信息

Institut de Biotechnologie des Plantes, Universite de Paris-Sud, Orsay, France.

出版信息

Cytometry. 1996 Mar 1;23(3):241-9. doi: 10.1002/(SICI)1097-0320(19960301)23:3<241::AID-CYTO7>3.0.CO;2-L.

Abstract

Phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) is a key enzyme of photosynthesis in C4 plants; it is specifically localized in the cytosol of mesophyll cells and is regulated by a phosphorylation/dephosphorylation process. The light-dependent phosphorylation of PEPC is triggered by an increase in the cytosolic pH (pHc) of mesophyll cell protoplasts. An epifluorescence and confocal microscopy analysis showed that the specific pH probe 2',7'-bis-(2-carboxyethyl)-5-(and-6) carboxyfluorescein, acetoxymethyl ester (BCECF-AM), when used at low concentration, was essentially localized in the protoplast cytosol. By the nigericin null-point method and flow cytometry, the pHc of freshly isolated protoplasts was estimated to be 6.4. To observe the full activity of PEPC kinase and maximal phosphorylation of PEPC in vivo, such protoplast suspensions must first be treated with a permeant weak base. The present report shows that 20 mM NH4Cl raised the final pHc to 7.4. This method can be useful for estimating rapid changes of pHc in plant cells.

摘要

磷酸烯醇式丙酮酸羧化酶(PEPC,EC 4.1.1.31)是C4植物光合作用的关键酶;它特异性地定位于叶肉细胞的细胞质中,并受磷酸化/去磷酸化过程的调节。PEPC的光依赖性磷酸化由叶肉细胞原生质体细胞质pH值(pHc)的升高触发。落射荧光和共聚焦显微镜分析表明,低浓度使用时,特异性pH探针2',7'-双(2-羧乙基)-5-(和-6)羧基荧光素乙酰氧基甲酯(BCECF-AM)主要定位于原生质体细胞质中。通过尼日利亚菌素零点法和流式细胞术,新鲜分离的原生质体的pHc估计为6.4。为了在体内观察PEPC激酶的完全活性和PEPC的最大磷酸化,此类原生质体悬浮液必须首先用渗透性弱碱处理。本报告表明,20 mM NH4Cl可将最终pHc提高到7.4。该方法可用于估计植物细胞中pHc的快速变化。

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