Hunter D R, Segel I H
J Bacteriol. 1973 Mar;113(3):1184-92. doi: 10.1128/jb.113.3.1184-1192.1973.
A variety of weak acids at and below their pK(a) are potent inhibitors of transport in Penicillium chrysogenum. The effective compounds include sorbate, benzoate, and propionate (common antifungal agents), indoleacetate (a plant hormone), acetylsalicylate (aspirin), hexachlorophene, and a yellow pigment produced by the mycelia under nutrient-deficient conditions, as well as the classical uncouplers 2,4-dinitrophenol, p-nitrophenol, and azide. The results suggest that a proton gradient or charge gradient is involved in energizing membrane transport in P. chrysogenum. The unionized form of the weak acids could discharge the gradient by diffusing through the membrane and ionizing when they reach an interior compartment of higher pH. Experiments with 2,4-dinitrophenol and p-nitrophenol established that the ionized species are not absorbed by the mycelium to any great extent. The transport inhibitors also caused a decrease in cellular adenosine 5'-triphosphate (ATP) levels, but there was no constant correlation between inhibition of transport and suppression of cellular ATP. A decrease in aeration of the mycelial suspension had the same effect on transport and ATP levels as the addition of a weak organic acid. The effects on transport rates and ATP levels were reversible. The instantaneous inhibition of [(14)C]l-leucine transport by NH(4) (-) (and vice-versa) in nitrogen-starved mycelia at pH values of 7 or below can be explained by competition for a common energy-coupling system. The inhibition is not observed in carbon-starved mycelia in which the NH(4) (+) transport system is absent or inactive (but the general amino acid transport is fully active), or in iodoacetate-treated mycelia in which the NH(4) (+) transport system has been differentially inactivated. At pH values greater than 7.0, NH(3) and HPO(4) (2-) inhibit transport, presumably by discharging the membrane proton or charge gradient. Aniline counteracts the inhibitory effect of NH(3) and HPO(4) (2-) possibly by acting as a proton reservoir or buffer within the membrane.
多种处于或低于其pK(a)值的弱酸是产黄青霉中转运的有效抑制剂。有效化合物包括山梨酸、苯甲酸和丙酸(常见的抗真菌剂)、吲哚乙酸(一种植物激素)、乙酰水杨酸(阿司匹林)、六氯酚以及在营养缺乏条件下由菌丝体产生的一种黄色色素,还有经典的解偶联剂2,4 - 二硝基苯酚、对硝基苯酚和叠氮化物。结果表明质子梯度或电荷梯度参与了产黄青霉中膜转运的能量供应。弱酸的 unionized形式可以通过扩散穿过膜并在到达较高pH值的内部隔室时电离来消除梯度。用2,4 - 二硝基苯酚和对硝基苯酚进行的实验表明,离子化形式在很大程度上不会被菌丝体吸收。转运抑制剂还导致细胞腺苷5'-三磷酸(ATP)水平降低,但转运抑制与细胞ATP抑制之间没有恒定的相关性。菌丝体悬浮液通气减少对转运和ATP水平的影响与添加弱有机酸相同。对转运速率和ATP水平的影响是可逆的。在pH值为7或更低时,氮饥饿菌丝体中NH(4) (-) 对[(14)C]l - 亮氨酸转运的瞬时抑制(反之亦然)可以通过对共同能量偶联系统的竞争来解释。在碳饥饿菌丝体中未观察到这种抑制,其中NH(4) (+) 转运系统不存在或无活性(但一般氨基酸转运完全活跃),或者在碘乙酸处理的菌丝体中,NH(4) (+) 转运系统已被差异失活。在pH值大于7.0时,NH(3) 和HPO(4) (2-) 抑制转运,可能是通过消除膜质子或电荷梯度。苯胺可能通过作为膜内的质子储存器或缓冲剂来抵消NH(3) 和HPO(4) (2-) 的抑制作用。