Storey B T
Plant Physiol. 1970 Apr;45(4):447-54. doi: 10.1104/pp.45.4.447.
The half-time for oxidation of cytochrome b(557) in mitochondria from etiolated mung bean (Phaseolus aureus) hypocotyls is 5.8 milliseconds at 24 Celsius in the absence or presence of 0.3 mm KCN, when the oxidation is carried out by injecting a small amount of oxygenated medium into a suspension of mitochondria made anaerobic in the presence of succinate plus malonate. Since oxygen is consumed by the alternate, cyanide-insensitive respiratory pathway of these mitochondria, cycles of oxidation and reduction can be obtained with the oxygen pulses when cyanide is present. Reduced cytochromes (a + a(3)) also become oxidized at nearly the uninhibited rate under these conditions, a(3) completely and a partially. The half-time for oxidation of c(547) is also unaffected by 0.3 mm KCN, but c(549) has a half-time equal to that of c(547) in the presence of KCN, compared to the shorter one observed in the absence of inhibitor. The maximum extent of oxidation of the cytochromes c is about 70% in the presence of 0.3 mm KCN; this oxidation is rapidly followed by an extensive reduction which is synchronous with the reduction of cytochrome a observed under the same conditions. In the presence of cyanide, it appears likely that the cytochromes c and b(557) are oxidized by cytochrome oxidase in oxygen pulse experiments, rather than by the alternate oxidase. The oxidation of cytochrome b(553) is partially inhibited by KCN, but complete oxidation is attained in the aerobic steady state with excess oxygen. If the oxygen pulse experiment is carried out in the presence of sufficient malonate so that entry of reducing equivalents into the respiratory chain occurs at a rate negligible compared to inter-carrier electron transport, the half-time for flavoprotein oxidation is unaffected by 0.3 mm KCN while that for ubiquinone oxidation is but 2-fold larger. The observed net oxidation rate of these two carriers in mung bean mitochondria is more sensitive to the entry rate of reducing equivalents, as set by succinate concentration and malonate to succinate ratio, then it is in skunk cabbage (Symplocarpus foetidus) mitochondria. These observations are interpreted in terms of a respiratory carrier Y, placed between flavoprotein plus ubiquinone and the cytochromes, which is the fork in the split respiratory pathway to the two terminal oxidases and which has lower electron transport capacity in mung bean mitochondria than in skunk cabbage mitochondria.
在24摄氏度下,当通过向在琥珀酸加丙二酸存在下已变为厌氧的线粒体悬浮液中注入少量充氧培养基来进行氧化时,在有无0.3 mM KCN的情况下,黄化绿豆(Phaseolus aureus)下胚轴线粒体中细胞色素b(557)氧化的半衰期为5.8毫秒。由于这些线粒体的交替、对氰化物不敏感的呼吸途径会消耗氧气,因此当存在氰化物时,通过氧气脉冲可获得氧化和还原循环。在这些条件下,还原型细胞色素(a + a(3))也以接近未受抑制的速率被氧化,a(3)完全被氧化,a部分被氧化。细胞色素c(547)氧化的半衰期也不受0.3 mM KCN的影响,但与在无抑制剂时观察到的较短半衰期相比,细胞色素c(549)在有KCN存在时的半衰期与c(547)相同。在0.3 mM KCN存在下,细胞色素c的最大氧化程度约为70%;这种氧化之后迅速伴随着广泛的还原,这与在相同条件下观察到的细胞色素a的还原是同步的。在有氰化物存在的情况下,在氧气脉冲实验中,细胞色素c和b(557)似乎是被细胞色素氧化酶氧化,而不是被交替氧化酶氧化。细胞色素b(553)的氧化受到KCN的部分抑制,但在有氧稳态且有过量氧气的情况下可实现完全氧化。如果在存在足够丙二酸的情况下进行氧气脉冲实验,使得还原当量进入呼吸链的速率与载体间电子传递速率相比可忽略不计,那么黄素蛋白氧化的半衰期不受0.3 mM KCN的影响,而泛醌氧化的半衰期仅增大2倍。在绿豆线粒体中观察到的这两种载体的净氧化速率对还原当量的进入速率更为敏感,还原当量的进入速率由琥珀酸浓度和丙二酸与琥珀酸的比例决定,这一点比在臭菘(Symplocarpus foetidus)线粒体中更明显。这些观察结果是根据呼吸载体Y来解释的,Y位于黄素蛋白加泛醌和细胞色素之间,是通向两种末端氧化酶的分支呼吸途径中的分支点,并且在绿豆线粒体中的电子传递能力低于臭菘线粒体。