Samuilov V D, Barsky E L
Department of Cell Physiology and Immunology, Moscow State University, Russian Federation.
FEBS Lett. 1993 Apr 5;320(2):118-20. doi: 10.1016/0014-5793(93)80074-5.
We show that CCCP, known as an uncoupler of photophosphorylation and an ADRY agent, inhibits FeCy photoreduction and coupled O2 evolution by isolated chloroplasts equally (I50 approximately 2 microM), but is practically without effect on the O2 evolution coupled with SiMo reduction within the 0.2-10 microM concentration range. CCCP has no effect on the nanosecond chlorophyll fluorescence in chloroplasts incubated at low light intensity, but decreases it at high light intensity. The electron transfer from reduced TMPD or duroquinol to methylviologen is resistant to CCCP. The efficiency of the CCCP inhibitory action on the FeCy photoreduction depends on the rate of electron flow, which is controlled by the light intensity. The data obtained show that CCCP is oxidized by the photosystem II donor side and is reduced by QP, competing for electrons with FeCy and the cytochrome blf complex.
我们发现,作为光合磷酸化解偶联剂和一种ADRY试剂的CCCP,对分离的叶绿体抑制铁氰化物光还原和偶联的氧气释放具有同等效力(I50约为2 microM),但在0.2 - 10 microM浓度范围内对与硅钼酸盐还原偶联的氧气释放几乎没有影响。CCCP对在低光强度下孵育的叶绿体中的纳秒叶绿素荧光没有影响,但在高光强度下会使其降低。从还原的四甲基对苯二胺或杜罗醌到甲基紫精的电子转移对CCCP具有抗性。CCCP对铁氰化物光还原的抑制作用效率取决于电子流动速率,而电子流动速率由光强度控制。所获得的数据表明,CCCP在光系统II供体侧被氧化,并被QP还原,与铁氰化物和细胞色素blf复合物竞争电子。