{"title":"H+-ATPase and Auxin-stimulated ATPase in Membrane Fractions from Zucchini (Cucurbita pepo L.) and Pumpkin (Cucurbita maxima L.) hypocotyls","authors":"G.F.E. Scherer","doi":"10.1016/S0044-328X(84)80016-1","DOIUrl":null,"url":null,"abstract":"<div><p>We separated two membrane fractions containing H<sup>+</sup>-ATPase. One fraction with H<sup>+</sup>-ATPase was enriched in plasma membranes while the other one contained no plasma membranes. Since mitochondrial or plastidial origin of H<sup>+</sup>-ATPase could be excluded, the latter one presumably contained H<sup>+</sup>-ATPase in tonoplast vesicles.</p><p>With a plasma membrane-enriched fraction, the effect of auxin on ATPase activity was investigated. Auxin decreased the apparent K<sub>M</sub> of ATPase so that auxin stimulation of ATPase activity can be measured best at very low ATP concentrations (< 50 μM). The stimulation of ATPase activity is specific for auxin in that 2,3-dichlorophenoxyacetic acid, a weak auxin, had a much lower effects than 2,4-dichlorophenoxyacetic acid or indolyl-3-acetic acid.</p><p>These experiments support the hypothesis that auxin stimulates H<sup>+</sup>-extrusion by stimulation of a H<sup>+</sup>-ATPase <em>in vivo</em> and <em>in vitro</em>.</p></div>","PeriodicalId":23797,"journal":{"name":"Zeitschrift für Pflanzenphysiologie","volume":"114 3","pages":"Pages 233-237"},"PeriodicalIF":0.0000,"publicationDate":"1984-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0044-328X(84)80016-1","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für Pflanzenphysiologie","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0044328X84800161","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 14
Abstract
We separated two membrane fractions containing H+-ATPase. One fraction with H+-ATPase was enriched in plasma membranes while the other one contained no plasma membranes. Since mitochondrial or plastidial origin of H+-ATPase could be excluded, the latter one presumably contained H+-ATPase in tonoplast vesicles.
With a plasma membrane-enriched fraction, the effect of auxin on ATPase activity was investigated. Auxin decreased the apparent KM of ATPase so that auxin stimulation of ATPase activity can be measured best at very low ATP concentrations (< 50 μM). The stimulation of ATPase activity is specific for auxin in that 2,3-dichlorophenoxyacetic acid, a weak auxin, had a much lower effects than 2,4-dichlorophenoxyacetic acid or indolyl-3-acetic acid.
These experiments support the hypothesis that auxin stimulates H+-extrusion by stimulation of a H+-ATPase in vivo and in vitro.