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植物细胞表面的静电效应与酶反应动力学。1. 复杂多酶系统的离子控制理论。

Electrostatic effects and the dynamics of enzyme reactions at the surface of plant cells. 1. A theory of the ionic control of a complex multi-enzyme system.

作者信息

Ricard J, Noat G

出版信息

Eur J Biochem. 1986 Feb 17;155(1):183-90. doi: 10.1111/j.1432-1033.1986.tb09475.x.

Abstract

A theory is proposed to explain the physical bases of the ionic control of the activity of an enzyme system, located on a plant cell surface, and probably involved in cell-wall synthesis and extension. The model, which is based on various previously published experimental results, involves several assumptions: a cell-wall pectin methyl esterase de-esterifies pectins and thus creates the fixed negative charges of the cell wall; various enzymes incorporate uncharged carbohydrates in cell-wall material; cell-wall extension implies the sliding of cellulose microfibrils; the enzymes responsible for carbohydrate incorporation are activated by protons in the pH range 4-8 and have very similar pH dependencies: the cell-wall pectin methyl esterase is inhibited by protons in the same pH range. The mathematical derivation of this model, written in the form of a hypercycle, indicates that it is equivalent to a set of two antagonistic enzyme reactions: an enzyme reaction conditioned by pectin methyl esterase which results in the increase of fixed charge density of the cell wall; a number of 'growth enzymes', which produce extension and building up of the cell wall and therefore a decrease of charge density. The mathematical study of this model shows it may display a very high co-operativity of its response to slight changes of pH. This cooperativity means that the cell wall charge density may dramatically increase or decrease, within a very narrow pH range. The steep response of this system appears to be the direct consequence of different pH sensitivities of pectin methyl esterase and of the other cell-wall enzymes involved in cell growth. Calcium, which tightly binds to the cell wall, may diminish or even suppress this abrupt charge transition. This model suggests a novel theory of the ionic control of cell-wall expansion. The very basis of this theory is the existence of an electrostatic potential difference, delta psi, between the inside and the outside of the cell wall. When this delta psi value is large, the local proton concentration is high. Therefore the enzymes involved in cell wall extension and building up are active, but pectin methyl esterase is not. Therefore, the cell wall extends and the charge density decreases. The delta psi value then declines, as well as the local proton concentration. Under these conditions, the pectin methyl esterase becomes activated, whereas the 'growth enzymes' are not. This activation of pectin methyl esterase restores the initial, or an even higher, electrostatic potential difference, which in turn results in a decrease of local pH.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本文提出了一种理论,用以解释位于植物细胞表面、可能参与细胞壁合成与伸展的酶系统离子控制的物理基础。该模型基于先前发表的各种实验结果,包含几个假设:细胞壁果胶甲基酯酶使果胶脱酯,从而产生细胞壁的固定负电荷;多种酶将不带电荷的碳水化合物掺入细胞壁物质中;细胞壁伸展意味着纤维素微纤丝的滑动;负责碳水化合物掺入的酶在pH值4 - 8范围内被质子激活,且具有非常相似的pH依赖性:细胞壁果胶甲基酯酶在相同pH范围内被质子抑制。以超循环形式编写的该模型的数学推导表明,它等同于一组两个拮抗的酶反应:由果胶甲基酯酶调节的酶反应导致细胞壁固定电荷密度增加;多种“生长酶”,它们促进细胞壁的伸展和构建,从而使电荷密度降低。对该模型的数学研究表明,它对pH的微小变化可能表现出非常高的协同性。这种协同性意味着细胞壁电荷密度可能在非常窄的pH范围内急剧增加或减少。该系统的陡峭响应似乎是果胶甲基酯酶和参与细胞生长的其他细胞壁酶不同pH敏感性的直接结果。紧密结合在细胞壁上的钙可能会减少甚至抑制这种突然的电荷转变。该模型提出了一种细胞壁扩张离子控制的新理论。该理论的基础是细胞壁内外存在静电势差Δψ。当这个Δψ值很大时,局部质子浓度很高。因此,参与细胞壁伸展和构建的酶是活跃的,但果胶甲基酯酶不活跃。因此,细胞壁伸展且电荷密度降低。然后,Δψ值下降,局部质子浓度也下降。在这些条件下,果胶甲基酯酶被激活,而“生长酶”不被激活。果胶甲基酯酶的这种激活恢复了初始的或更高的静电势差,这反过来又导致局部pH值降低。(摘要截选至400字)

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