Camarasa C, Prieto S, Ros R, Salmon J M, Barre P
Institut des Produits de la Vigne, Institut de la Recherche Agronomique, Montpellier, France.
Yeast. 1996 Oct;12(13):1301-13. doi: 10.1002/(SICI)1097-0061(199610)12:13%3C1301::AID-YEA18%3E3.0.CO;2-A.
The existence of a K+/H+ transport system in plasma membrane vesicles from Saccharomyces cerevisiae is demonstrated using fluorimetric monitoring of proton fluxes across vesicles (ACMA fluorescence quenching). Plasma membrane vesicles used for this study were obtained by a purification/reconstitution protocol based on differential and discontinuous sucrose gradient centrifugations followed by an octylglucoside dilution/gel filtration procedure. This method produces a high percentage of tightly-sealed inside-out plasma membrane vesicles. In these vesicles, the K+/H+ transport system, which is able to catalyse both K+ influx and efflux, is mainly driven by the K+ transmembrane gradient and can function even if the plasma membrane H(+)-ATPase is not active. Using the anionic oxonol VI and the cationic DISC2(5) probes, it was shown that a membrane potential is not created during K+ fluxes. Such a dye response argues for the presence of a K+/H+ exchange system in S. cerevisiae plasma membrane and established the non-electrogenic character of the transport. The maximal rate of exchange is obtained at pH 6.8. This reversible transport system presents a high selectivity for K+ among other monovalent cations and a higher affinity for the K+ influx into the vesicles (exit from cells). The possible role of this K+/H+ exchange system in regulation of internal potassium concentration in S. cerevisiae is discussed.
通过荧光监测质子跨囊泡通量(ACMA荧光猝灭),证明了酿酒酵母质膜囊泡中存在K⁺/H⁺转运系统。用于本研究的质膜囊泡是通过基于差速和不连续蔗糖梯度离心,随后进行辛基葡糖苷稀释/凝胶过滤程序的纯化/重组方案获得的。该方法产生高比例的紧密密封的内向外质膜囊泡。在这些囊泡中,能够催化K⁺流入和流出的K⁺/H⁺转运系统主要由K⁺跨膜梯度驱动,即使质膜H⁺-ATP酶不活跃也能发挥作用。使用阴离子氧杂萘邻酮VI和阳离子DISC2(5)探针表明,在K⁺通量期间不会产生膜电位。这种染料反应表明酿酒酵母质膜中存在K⁺/H⁺交换系统,并确定了转运的非电生性特征。在pH 6.8时获得最大交换速率。这种可逆转运系统对其他单价阳离子中的K⁺具有高选择性,并且对K⁺流入囊泡(从细胞中流出)具有更高的亲和力。讨论了这种K⁺/H⁺交换系统在调节酿酒酵母内部钾浓度中的可能作用。