Junge W, Ausländer W, McGeer A J, Runge T
Biochim Biophys Acta. 1979 Apr 11;546(1):121-41. doi: 10.1016/0005-2728(79)90175-0.
The buffering capacity inside thylakoids is determined and the magnitude of flash-induced pH changes inside is calibrated in the pH range from 6.4 to 8.1. The work is based on flash-induced absorption changes of neutral red in a chloroplast suspension in which the outer phase is strongly buffered by bovine serum albumin. It is shown that neutral red is bound inside thylakoids. The binding can be described by a simple isotherm with an apparent Km = 4 microM and satruation at 1 neutral red per 17 chlorophylls. The apparent pK of neutral red is shifted from 6.6 in solution to 7.25 when bound inside. It is demonstrated that neutral red is a clean indicator of pH changes inside, i.e. when properly used it shows no response to other events. Although bound it reports pH changes which occur in the internal osmolar (aqueous) volume of thylakoids. This is obvious from the influence of chemically very different buffers on the magnitude of the absorption changes of neutral red. These act in a manner proportional to their calculated buffering capacity in aqueous solution. The intrinsic buffering capacity of the internal phase is determined with the aid of these buffers, at pH 7.2 it is between 0.8 and 1 mM (at 60 mosM). The absence of large variations in the buffering capacity in the range from pH 6.4 to 8.1 suggests that proteinaceous groups are involved in addition to the lipids which may dominate the buffering capacity at lower pH. The magnitude of the internal pH change is arrpox. 0.6 (at pH 7.3) under stimulation of both photosystems with a short xenon flash of light.
测定了类囊体内部的缓冲能力,并在6.4至8.1的pH范围内校准了闪光诱导的内部pH变化幅度。这项工作基于叶绿体悬浮液中中性红的闪光诱导吸收变化,其中外部相由牛血清白蛋白强烈缓冲。结果表明中性红结合在类囊体内部。这种结合可用一个简单的等温线来描述,表观Km = 4 microM,每17个叶绿素结合1个中性红时达到饱和。中性红的表观pK从溶液中的6.6移至结合在内部时的7.25。结果表明中性红是内部pH变化的一个纯净指示剂,即正确使用时它对其他事件无响应。尽管它是结合的,但能报告类囊体内部渗透(水相)体积中发生的pH变化。从化学性质差异很大的缓冲剂对中性红吸收变化幅度的影响可以明显看出这一点。这些缓冲剂的作用方式与其在水溶液中的计算缓冲能力成正比。借助这些缓冲剂确定了内相的固有缓冲能力,在pH 7.2时为0.8至1 mM(在60 mosM时)。在pH 6.4至8.1范围内缓冲能力没有大的变化,这表明除了在较低pH时可能主导缓冲能力的脂质外,蛋白质基团也参与其中。用短氙闪光同时刺激两个光系统时,内部pH变化幅度约为0.6(在pH 7.3时)。