Styring Stenbjörn, Feyziyev Yashar, Mamedov Fikret, Hillier Warwick, Babcock Gerald T
Department of Biochemistry, Centre for Chemistry and Chemical Engineering P.O. Box 124, Lund University, Sweden.
Biochemistry. 2003 May 27;42(20):6185-92. doi: 10.1021/bi027035r.
We have studied how low pH affects the water-oxidizing complex in Photosystem II when depleted of the essential Ca(2+) ion cofactor. For these samples, it was found that the EPR signal from the Y(Z)() radical decays faster at low pH than at high pH. At 20 degrees C, Y(Z)() decays with biphasic kinetics. At pH 6.5, the fast phase encompasses about 65% of the amplitude and has a lifetime of approximately 0.8 s, while the slow phase has a lifetime of approximately 22 s. At pH 3.9, the kinetics become totally dominated by the fast phase, with more than 90% of the signal intensity operating with a lifetime of approximately 0.3 s. The kinetic changes occurred with an approximate pK(a) of 4.5. Low pH also affected the induction of the so-called split radical EPR signal from the S(2)Y(Z)() state that is induced in Ca(2+)-depleted PSII membranes because of an inability of Y(Z)() to oxidize the S(2) state. At pH 4.5, about 50% of the split signal was induced, as compared to the amplitude of the signal that was induced at pH 6.5-7, using similar illumination conditions. Thus, the split-signal induction decreased with an apparent pK(a) of 4.5. In the same samples, the stable multiline signal from the S(2) state, which is modified by the removal of Ca(2+), was decreased by the illumination to the same extent at all pHs. It is proposed that decreased induction of the S(2)Y(Z)() state at lower pH was not due to inability to oxidize the modified S(2) state induced by the Ca(2+) depletion. Instead, we propose that the low pH makes Y(Z)() able to oxidize the S(2) state, making the S(2) --> S(3) transition available in Ca(2+)-depleted PSII. Implications of these results for the catalytic role of Ca(2+) and the role of proton transfer between the Mn cluster and Y(Z) during oxygen evolution is discussed.
我们研究了在去除必需的Ca(2+)离子辅因子时,低pH值如何影响光系统II中的水氧化复合物。对于这些样品,发现来自Y(Z)()自由基的电子顺磁共振(EPR)信号在低pH值下比在高pH值下衰减得更快。在20摄氏度时,Y(Z)()以双相动力学衰减。在pH 6.5时,快速相约占振幅的65%,寿命约为0.8秒,而慢速相的寿命约为22秒。在pH 3.9时,动力学完全由快速相主导,超过90%的信号强度的寿命约为0.3秒。动力学变化发生时的近似pK(a)为4.5。低pH值还影响了在Ca(2+)耗尽的PSII膜中由于Y(Z)()无法氧化S(2)状态而从S(2)Y(Z)()状态诱导出的所谓分裂自由基EPR信号的诱导。在pH 4.5时,与在pH 6.5 - 7时使用相似光照条件诱导的信号振幅相比,约50%的分裂信号被诱导。因此,分裂信号诱导随着表观pK(a)为4.5而降低。在相同样品中,来自S(2)状态的稳定多线信号(通过去除Ca(2+)而改变)在所有pH值下通过光照降低的程度相同。有人提出在较低pH值下S(2)Y(Z)()状态诱导的降低不是由于无法氧化由Ca(2+)耗尽诱导的修饰S(2)状态。相反,我们提出低pH值使Y(Z)()能够氧化S(2)状态,使得在Ca(2+)耗尽的PSII中S(2)→S(3)转变成为可能。讨论了这些结果对Ca(2+)的催化作用以及在氧气进化过程中质子在锰簇和Y(Z)之间转移的作用的影响。