Rose K A, Bearden A
Biochim Biophys Acta. 1980 Dec 3;593(2):342-52. doi: 10.1016/0005-2728(80)90071-7.
Electron paramagnetic resonance (EPR) power saturation and saturation recovery methods have been used to determine the spin lattice, T1, and spin-spin, T2, relaxation times of P-700+ reaction-center chlorophyll in Photosystem I of plant chloroplasts for 10 K less than or equal to T less than or equal to 100 K. T1 was 200 mus at 100 K and increased to 900 mus at 10 K. T2 was 40 ns at 40 K and increased to 100 ns at 10 K. T1 for 40 K less than or equal to T less than or equal to 100 K is inversely proportional to temperature, which is evidence of a direct-lattice relaxation process. At T = 20 K, T1 deviates from the 1/T dependence, indicating a cross relaxation process with an unidentified paramagnetic species. The individual effects of ascorbate and ferricyanide on T1 of P-700+ were examined: T1 of P-700+ was not affected by adding 10 mM ascorbate to digitonin-treated chloroplast fragments (D144 fragments). The P-700+ relaxation time in broken chloroplasts treated with 10 mM ferricyanide was 4-times shorter than in the untreated control at 40 K. Ferricyanide appears to be relaxing the P-700+ indirectly to the lattice by a cross-relaxation process. The possibility of dipolar-spin broadening of P-700+ due to either the iron sulfur center A or plastocyanin was examined by determining the spin-packet linewidth for P-700+ when center A and plastocyanin were in either the reduced or oxidized states. Neither reduced center A nor oxidized plastocyanin was capable of broadening the spin-packet linewidth of P-700+ signal. The absence of dipolar broadening indicates that both center A and plastocyanin are located at a distance at least 3.0 nm from the P-700+ reaction center chlorophyll. This evidence supports previous hypotheses that the electron donor and acceptor to P-700 are situated on opposite sides of the chloroplast membrane. It is also shown that the ratio of photo-oxidized P-700 to photoreduced centers A and B at low temperature is 2 : 1 if P-700 is monitored at a nonsaturating microwave power.
电子顺磁共振(EPR)功率饱和及饱和恢复方法已被用于测定植物叶绿体光系统I中P - 700 +反应中心叶绿素的自旋晶格弛豫时间T1和自旋 - 自旋弛豫时间T2,温度范围为10K≤T≤100K。T1在100K时为200微秒,在10K时增至900微秒。T2在40K时为40纳秒,在10K时增至100纳秒。40K≤T≤100K时,T1与温度成反比,这是直接晶格弛豫过程的证据。在T = 20K时,T1偏离1/T依赖关系,表明存在与未识别顺磁物种的交叉弛豫过程。研究了抗坏血酸盐和铁氰化物对P - 700 +的T1的单独影响:向洋地黄皂苷处理的叶绿体片段(D144片段)中添加10 mM抗坏血酸盐不会影响P - 700 +的T1。在40K时,用10 mM铁氰化物处理的破碎叶绿体中P - 700 +的弛豫时间比未处理的对照短4倍。铁氰化物似乎通过交叉弛豫过程将P - 700 +间接弛豫到晶格。通过测定当中心A和质体蓝素处于还原或氧化状态时P - 700 +的自旋包络线宽,研究了由于铁硫中心A或质体蓝素导致P - 700 +偶极 - 自旋展宽的可能性。还原态的中心A和氧化态的质体蓝素均不能加宽P - 700 +信号的自旋包络线宽。不存在偶极展宽表明中心A和质体蓝素均位于距P - 700 +反应中心叶绿素至少3.0纳米的距离处。这一证据支持了先前的假设,即P - 700的电子供体和受体位于叶绿体膜的两侧。研究还表明,如果在非饱和微波功率下监测P - 700,低温下光氧化的P - 700与光还原的中心A和B的比例为2:1。