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A Plasmamembrane Redox System and Proton Transport in Isolated Mesophyll Cells

机译:质膜氧化还原系统和质子在孤立的叶肉细胞中的运输。

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摘要

Potassium ferricyanide (K3Fe[CN]6) was added to aerated and stirred nonbuffered suspensions of mechanically isolated photosynthetically competent Asparagus sprengeri Regel mesophyll cells. Rates of Fe(CN)63− reduction and H+ efflux were measured with or without illumination. On the addition of 1 millimolar Fe(CN)63− to nonilluminated cell suspensions acidification of the medium indicated an H+ efflux of 1.54 nanomoles H+/106 cells per minute. Simultaneous Fe(CN)63− reduction occurred at a rate of 1.55 nanomoles Fe(CN)63−/106 cells per minute. Illumination stimulated these rates 14 to 17 times and corresponding values were 26.1 nanomoles H+/106 cells per minute and 22.9 nanomoles Fe(CN)63−/106 cells per minute. These two processes appeared to be tightly coupled and were rapidly inhibited when illuminated suspensions were transferred to darkness or treated with 1 micromolar 3-(3,4-dichlorophenyl)-1,1 dimethylurea. Addition of 0.1 millimolar diethylstilbestrol eliminated ATP dependent H+ efflux in illuminated or nonilluminated cells but had no influence on Fe(CN)63− dependent H+ efflux. Recent reports indicate that a transmembrane redox system spans the plasma membrane of root cells and is coupled to the efflux of H+. The present report extends these observations to photosynthetically competent mesophyll cells. The results indicate a transport process independent of ATP driven H+ efflux which operates with a H+/e stoichiometry of one.
机译:将铁氰化钾(K3Fe [CN] 6)添加到机械分离的光合作用的芦笋瑞格勒Regel叶肉细胞的充气和搅拌的非缓冲悬浮液中。在有或没有照明的情况下测量Fe(CN)6 3-的还原率和H + 的外排率。在未光照的细胞悬浮液中添加1毫摩尔Fe(CN)6 3-时,介质的酸化表明H + 的流出量为1.54纳摩尔H + / 10 6 个细胞。 Fe(CN)6 3-的同时还原速率为1.55纳摩尔Fe(CN)6 3- / 10 6 细胞/分钟。照明将这些速率刺激了14到17倍,相应的值为每分钟26.1纳摩尔H + / 10 6 细胞和22.9纳摩尔Fe(CN)6 3− < / sup> / 10 6 每分钟。当将照明的悬浮液转移到黑暗中或用1微摩尔的3-(3,4-二氯苯基)-1,1二甲基脲处理时,这两个过程似乎紧密耦合并被迅速抑制。添加0.1毫摩尔的己烯雌酚可消除光照或未光照细胞中ATP依赖的H + 外流,但对Fe(CN)6 3 − 依赖的H + 无影响sup>外排。最近的报道表明跨膜氧化还原系统跨过根细胞的质膜,并与H + 的流出有关。本报告将这些发现扩展到光合作用的叶肉细胞。结果表明运输过程独立于ATP驱动的H + 外排,其化学计量比为H + / e -

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