Altendorf K, Hirata H, Harold F M
J Biol Chem. 1975 Feb 25;250(4):1405-12.
We have studied the accumulation of dibenzyldimethyl-ammonium ion (DDA+) by respiring membrane vesicles of Escherichia coli, as an index of the generation of an electrical gradient during respiration. Nonrespiring vesicles accumulated DDA+ when K+ efflux was induced by valinomycin or monactin. By various criteria this was shown to be the exchange of one cation for another, independent of metabolism and coupled entirely by electrical forces. Uptake of DDA+ by respiring vesicles was inhibited by ionophores that translocate electrical charge and by reagents that block the respiratory chain. Oxamate and p-chloromercuribenzoate inhibited accumulation of DDA+ but did not dissipate a preformed pool; the reason appears to be that these reagents are less inhibitory to transport after lactate oxidation has begun than they are in resting vesicles. Uptake does not appear to involve a biological carrier, but requires trace amounts of a lipid-soluble anion such as tetraphenylboron, which has a catalytic role in DDA+ translocation. Respiring K+ vesicles accumulated substantially less DDA+ than did Na+ vesicles. Na+ was expelled from the vesicles concurrently with DDA+ uptake, whereas Rb+ and K+ were not. Thus, DDA+ uptake, whereas Rb+ and K+ were not. Thus, DDA+ uptake may be limited in the latter case by the availability of anionic groups. This explanation was supported by the finding that the addition of nigericin doubled the capacity of K+ vesicles to take up DDA+, presumably by providing a route for K+ to exit in exchange for H+. Parallel experiments on the valinomycin-dependent accumulation of Rb+ by respiring vesicles indicate that this process is analogous to the uptake of DDA+. Ionophores that elicit electrogenic K+ movement also induced respiration-linked transport. Proton-conducting ionophores and several inhibitors of respiration block Rb+ uptake and dissipated a preformed gradient. Preincubation of the vesicles with oxamate or p-chloromercuribenzoate inhibited Rb+ uptake, but their addition to respiring vesicles again did not cause efflux. Rb+ and DDA+ complete for uptake when present simultaneously. We conclude that the accumulation of both DDA+ and Rb+ occurs in response to an electrical gradient, vesicle interior negative, produced by respiration.
我们研究了大肠杆菌呼吸膜囊泡对二苄基二甲基铵离子(DDA+)的积累情况,以此作为呼吸过程中产生电梯度的指标。当缬氨霉素或莫能菌素诱导钾离子外流时,不呼吸的囊泡会积累DDA+。通过各种标准表明,这是一种阳离子与另一种阳离子的交换,与代谢无关,完全由电力耦合。呼吸囊泡对DDA+的摄取受到能转运电荷的离子载体和阻断呼吸链的试剂的抑制。草氨酸盐和对氯汞苯甲酸抑制DDA+的积累,但不会消耗预先形成的池;原因似乎是这些试剂在乳酸氧化开始后对转运的抑制作用比对静止囊泡中的抑制作用小。摄取似乎不涉及生物载体,但需要微量的脂溶性阴离子,如四苯基硼,它在DDA+转运中起催化作用。呼吸的钾离子囊泡积累的DDA+比钠离子囊泡少得多。钠离子在DDA+摄取的同时从囊泡中排出,而铷离子和钾离子则不会。因此,在后一种情况下,DDA+的摄取可能受到阴离子基团可用性的限制。这一解释得到了以下发现的支持:添加尼日利亚菌素使钾离子囊泡摄取DDA+的能力增加了一倍,大概是通过提供一条钾离子以交换氢离子的方式排出的途径。对呼吸囊泡中缬氨霉素依赖性铷离子积累的平行实验表明,这个过程类似于DDA+的摄取。引发电致钾离子运动的离子载体也诱导了呼吸相关的转运。质子传导离子载体和几种呼吸抑制剂阻断铷离子摄取并消除预先形成的梯度。用草氨酸盐或对氯汞苯甲酸对囊泡进行预孵育会抑制铷离子摄取,但将它们添加到呼吸囊泡中同样不会导致外流。当同时存在时,铷离子和DDA+竞争摄取。我们得出结论,DDA+和铷离子的积累都是对呼吸产生的电梯度(囊泡内部为负)的反应。