Slavík J, Kotyk A
Biochim Biophys Acta. 1984 Sep 27;766(3):679-84. doi: 10.1016/0005-2728(84)90129-4.
The pH-dependent fluorescence excitation of fluorescein located intracellularly and in the vicinity of cells of the yeast Saccharomyces cerevisiae and Endomyces magnusii was used to obtain local pH values at a linear resolution 0.2 micron. Cells suspended in water or in a diluted (5 mM) acidic buffer had a relatively alkaline interior (about 7.0-7.5) with pH decreasing gradually toward the periphery and further out through the cell wall to the value of the bulk solution. In slightly alkaline weak buffers the cells also showed an alkaline center and a slightly acidic ring-shaped area, but the peripheral region close to the membrane was again alkaline with pH increasing toward the bulk solution. The heterogeneity of intracellular pH was reduced or nearly abolished in starved or antimycin-treated cell. Suspension of cells in strong (200 mM) buffer resulted within 15-20 min in a nearly homogeneous pH pattern throughout the cell, attaining pH values of 5.5-7.5, depending on the pH of the buffer. Addition of glucose with concomitant pH decrease of the extracellular medium did not change appreciably the intracellular pattern for 20-30 min, except with diethylstilbestrol (inhibitor of proton-extruding ATPase) when the cell became more acidic. It appears that the delta pH measurements between the cell as a whole and the bulk solution (as are used for the calculation of the electrochemical potential of protons in proton-driven transports) are not substantiated, the probable pH difference across the plasma membrane being substantially smaller than previously supposed.
利用位于酿酒酵母和大形内孢霉细胞内及细胞附近的荧光素的pH依赖性荧光激发,以0.2微米的线性分辨率获取局部pH值。悬浮于水或稀释(5 mM)酸性缓冲液中的细胞内部相对呈碱性(约7.0 - 7.5),pH值朝着周边逐渐降低,并通过细胞壁进一步向外降至整体溶液的值。在微碱性的弱缓冲液中,细胞也显示出碱性中心和微酸性的环形区域,但靠近膜的周边区域再次呈碱性,pH值朝着整体溶液增加。在饥饿或经抗霉素处理的细胞中,细胞内pH的异质性降低或几乎消除。将细胞悬浮于强(200 mM)缓冲液中,15 - 20分钟内细胞内会形成几乎均匀的pH模式,pH值达到5.5 - 7.5,具体取决于缓冲液的pH值。添加葡萄糖并伴随细胞外培养基pH降低,在20 - 30分钟内细胞内模式没有明显变化,但使用己烯雌酚(质子泵出ATP酶抑制剂)时细胞会变得更酸。似乎整体细胞与整体溶液之间的ΔpH测量值(用于计算质子驱动转运中质子的电化学势)没有依据,质膜两侧可能的pH差异远小于先前的推测。