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金黄色葡萄球菌的膜电位与庆大霉素摄取

Membrane potential and gentamicin uptake in Staphylococcus aureus.

作者信息

Mates S M, Eisenberg E S, Mandel L J, Patel L, Kaback H R, Miller M H

出版信息

Proc Natl Acad Sci U S A. 1982 Nov;79(21):6693-7. doi: 10.1073/pnas.79.21.6693.

Abstract

At pH 5.0, the electrical potential (delta psi, interior negative) across the plasma membrane of Staphylococcus aureus exhibits a minimum of -85 to -90 mV; the pH gradient (delta pH, interior alkaline) across the membrane approximates a maximum of about -100 mV. Under these conditions, uptake of the aminoglycoside gentamicin is negligible, and viability of the organism is not impaired by the antibiotic. In contrast, at pH 7.5, at which delta psi is about -130 mV and delta pH is 0, gentamicin uptake is observed and the drug markedly decreases viability. Dramatically, when the ionophore nigericin is added at pH 5.0, gentamicin uptake is induced, there is a striking decrease in viability, and the effect is associated with an increase in delta psi at the expense of delta pH. Consistently, valinomycin, which dissipates delta psi in the presence of potassium, abolishes gentamicin uptake and killing. In addition, from pH 5.0 to pH 7.5, there is a direct relationship between the magnitude of delta psi and both gentamicin uptake and its bactericidal effect. However, a threshold delta psi of -75 to -90 mV is apparently necessary to initiate uptake and killing. These observations provide a strong indication that delta psi plays a critical role in the uptake and antibacterial action of gentamicin and suggest that nigericin-like ionophores may be clinically useful in synergy with aminoglycosides.

摘要

在pH 5.0时,金黄色葡萄球菌质膜上的电势(Δψ,内部为负)呈现出-85至-90 mV的最小值;跨膜的pH梯度(ΔpH,内部为碱性)最大约为-100 mV。在这些条件下,氨基糖苷类庆大霉素的摄取可忽略不计,且该生物体的活力不受抗生素损害。相比之下,在pH 7.5时,Δψ约为-130 mV且ΔpH为0,此时可观察到庆大霉素的摄取,且该药物显著降低了活力。引人注目的是,当在pH 5.0时添加离子载体尼日利亚菌素,可诱导庆大霉素的摄取,活力显著下降,且这种效应与以ΔpH为代价的Δψ增加有关。一致地,在有钾存在时会消除Δψ的缬氨霉素,会消除庆大霉素的摄取和杀伤作用。此外,从pH 5.0到pH 7.5,Δψ的大小与庆大霉素的摄取及其杀菌作用之间存在直接关系。然而,启动摄取和杀伤作用显然需要-75至-90 mV的阈值Δψ。这些观察结果有力地表明,Δψ在庆大霉素的摄取和抗菌作用中起关键作用,并表明尼日利亚菌素样离子载体可能在与氨基糖苷类药物协同作用时具有临床应用价值。

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