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首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >Proton flows across the plasma membrane in microperforated characean internodes: tonoplast injury and involvement of cytoplasmic streaming
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Proton flows across the plasma membrane in microperforated characean internodes: tonoplast injury and involvement of cytoplasmic streaming

机译:质子流过微孔查理人节间质膜:液泡膜损伤和胞浆流

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摘要

Microperforation of characean cell wallwith a glass micropipette in the absence of the tonoplast impalement was found to cause rapid alkalinization of the apoplast by 2–3 pH units, which may rigidify the cell wall structure, thus protecting the cell from further injury. A similar but a deeper insertion of a microneedle, associated with piercing the tonoplast and with an action potential generation, led to a considerable delay in the apoplast alkalinization without affecting the amplitude of the eventual increase in pH. The retardation by the mechanically elicited action potential of the incisionmediated pH transients in the apoplast contrasted sharply to the enhancement of these pH transients by the action potential triggered electrically before the microperforation. Hence, the delay of the apoplast alkalinization was not related to basic ionic mechanisms of plant action potentials.Measurements of the vacuolar pH after mechanical elicitation of an action potential indicate that the tonoplast piercing was accompanied by leakage of protons from the vacuole into the cytoplasm, which may strongly acidify the cytoplasm around the wounded area, thus collapsing the driving force for H~+ influx from the medium into the cytoplasm. The lag period preceding the onset of external alkalinization was found linearly related to the duration of temporal cessation of cytoplasmic streaming. The results suggest that the delayed alkalinization of the apoplast in the region of tonoplast wounding reflects the localized recovery of the proton motive force across the plasmalemma during replacement of the acidic cytoplasm with fresh portions of unimpaired cytoplasm upon restoration of cytoplasmic streaming.
机译:发现在没有液泡膜穿刺的情况下,用玻璃微量移液器对查理亚细胞壁进行微穿孔会导致质子体迅速碱化2-3个pH单位,这可能会使细胞壁结构变硬,从而保护细胞免受进一步伤害。微针的类似但更深的插入,与刺穿液泡膜并产生动作电位有关,导致质外体碱化的相当大的延迟,而不会影响pH最终升高的幅度。由机械诱导的外生质子中切口介导的pH瞬变引起的阻滞与微穿孔前电触发的动作电位对这些pH瞬变的增强形成鲜明对比。因此,质外体碱化的延迟与植物动作电位的基本离子机制无关。机械激发动作电位后液泡pH的测量表明,液泡膜的刺穿伴随着质子从液泡渗入细胞质,这可能会强烈酸化伤口周围的细胞质,从而使H〜+从培养基流入细胞质的驱动力瓦解。发现外部碱化开始之前的滞后时间与细胞质流暂时停止的时间线性相关。结果表明,在液泡膜损伤区域中的质外体的延迟碱化反映了在细胞质流恢复后,用新鲜的未受损细胞质部分替换酸性细胞质时,质子动力跨质膜局部恢复。

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