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Selectivity of alkali cation influx across the plasma membrane of oat roots: cation specificity of the plasma membrane ATPase.选择通过燕麦根质膜的碱金属阳离子内流:质膜 ATP 酶的阳离子特异性。
Plant Physiol. 1977 Apr;59(4):641-6. doi: 10.1104/pp.59.4.641.
2
Characterization of Plasma Membrane-associated Adenosine Triphosphase Activity of Oat Roots.燕麦根质膜结合腺苷三磷酸酶活性的表征。
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Inhibition of adenosine triphosphatase activity of the plasma membrane fraction of oat roots by diethylstilbestrol.二苯乙烯基雌二醇对燕麦根质膜部分三磷酸腺苷酶活性的抑制作用。
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Effect of diethylstilbestrol on ion fluxes in oat roots.己烯雌酚对燕麦根离子通量的影响。
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Purification of plasma membranes from roots of barley: specificity of the phosphotungstic Acid-chromic Acid stain.大麦根质膜的纯化:磷钨酸-铬酸染色的特异性
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本文引用的文献

1
Characterization of Plasma Membrane-associated Adenosine Triphosphase Activity of Oat Roots.燕麦根质膜结合腺苷三磷酸酶活性的表征。
Plant Physiol. 1973 Jul;52(1):6-12. doi: 10.1104/pp.52.1.6.
2
Some Observations on Absorption of Cesium by Excised Barley Roots.关于大麦离体根对铯吸收的一些观察
Plant Physiol. 1960 Sep;35(5):605-8. doi: 10.1104/pp.35.5.605.
3
Role of Calcium in Absorption of Monovalent Cations.钙在单价阳离子吸收中的作用。
Plant Physiol. 1960 May;35(3):352-8. doi: 10.1104/pp.35.3.352.
4
A KINETIC STUDY OF THE ABSORPTION OF ALKALI CATIONS BY BARLEY ROOTS.大麦根对碱金属阳离子吸收的动力学研究
Plant Physiol. 1952 Jul;27(3):457-74. doi: 10.1104/pp.27.3.457.
5
SELECTIVE ABSORPTION OF CATIONS BY HIGHER PLANTS.高等植物对阳离子的选择性吸收
Plant Physiol. 1941 Oct;16(4):691-720. doi: 10.1104/pp.16.4.691.
6
Purification of an ion-stimulated adenosine triphosphatase from plant roots: association with plasma membranes.从植物根系中纯化离子刺激的三磷酸腺苷酶:与质膜的关联
Proc Natl Acad Sci U S A. 1972 Nov;69(11):3307-11. doi: 10.1073/pnas.69.11.3307.
7
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
8
Cation selective glass electrodes and their mode of operation.阳离子选择性玻璃电极及其工作模式。
Biophys J. 1962 Mar;2(2 Pt 2):259-323. doi: 10.1016/s0006-3495(62)86959-8.
9
Chemiosmotic coupling in oxidative and photosynthetic phosphorylation.氧化磷酸化和光合磷酸化中的化学渗透偶联
Biol Rev Camb Philos Soc. 1966 Aug;41(3):445-502. doi: 10.1111/j.1469-185x.1966.tb01501.x.
10
Biological membranes: the physical basis of ion and nonelectrolyte selectivity.生物膜:离子与非电解质选择性的物理基础。
Annu Rev Physiol. 1969;31:581-646. doi: 10.1146/annurev.ph.31.030169.003053.

选择通过燕麦根质膜的碱金属阳离子内流:质膜 ATP 酶的阳离子特异性。

Selectivity of alkali cation influx across the plasma membrane of oat roots: cation specificity of the plasma membrane ATPase.

机构信息

Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907.

出版信息

Plant Physiol. 1977 Apr;59(4):641-6. doi: 10.1104/pp.59.4.641.

DOI:10.1104/pp.59.4.641
PMID:16659910
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC542465/
Abstract

Influx of alkali cations (Li(+), Na(+), K(+), Rb(+), Cs(+)) across plasma membranes of cells of excised roots of Avena sativa cv. Goodfield was selective, but different, in the absence and in the presence of 1 mm CaSO(4). Ca(2+) reduced the influx rates of all of the alkali cations-especially Na(+) and Li(+). Transport selectivity changed as the external concentrations of the alkali cations increased.Plasma membrane ATPase, purified from Avena sativa roots, was differentially stimulated by alkali cations. This specificity, however, was not altered by Ca(2+) or the external cation concentrations. A close correspondence existed between the relative influx rates of K(+), Rb(+), and Cs(+) and the relative stimulation of the ATPase by these cations. A similar correspondence did not occur for Na(+) and Li(+).Selective cation transport in oat roots could result, in part, from the specificity of the plasma membrane ATPase, but other factors such as specific carriers or porters or differential diffusion rates must also be involved.

摘要

细胞外碱金属阳离子(Li(+)、Na(+)、K(+)、Rb(+)、Cs(+))流入燕麦 cv. Goodfield 去根切段细胞的质膜是有选择性的,但在 1mm CaSO(4) 存在或不存在的情况下,这种选择性是不同的。Ca(2+) 降低了所有碱金属阳离子的流入速率——尤其是 Na(+) 和 Li(+)。随着外部碱金属阳离子浓度的增加,运输选择性发生了变化。从燕麦根中纯化的质膜 ATP 酶被碱金属阳离子不同程度地刺激。然而,Ca(2+) 或外部阳离子浓度并没有改变这种特异性。K(+)、Rb(+) 和 Cs(+) 的相对流入速率与这些阳离子对 ATP 酶的相对刺激之间存在密切的相关性。Na(+) 和 Li(+) 则没有出现这种相关性。燕麦根中的选择性阳离子转运可能部分归因于质膜 ATP 酶的特异性,但也必须涉及其他因素,如特定的载体或门控蛋白或不同的扩散速率。