Hays A M, Vassiliev I R, Golbeck J H, Debus R J
Department of Biochemistry, University of California at Riverside 92521-0129, USA.
Biochemistry. 1999 Sep 14;38(37):11851-65. doi: 10.1021/bi990716a.
To further characterize the role of D1-His190 in the oxidation of tyrosine Y(Z) in photosystem II, the pH dependence of P(680)()()(+) reduction was measured in H190A and Mn-depleted wild-type PSII particles isolated from the cyanobacterium, Synechocystis sp. PCC 6803. Measurements were conducted in the presence and absence of imidazole and other small organic bases. In H190A PSII particles, rapid reduction of P(680)()()(+) attributed to electron transfer from Y(Z) increased dramatically above pH 9, with an apparent pK(A) of approximately 10.3. In the presence of ethanolamine and imidazole, this dramatic increase occurred at lower pH values, with the efficiency of Y(Z) oxidation correlating with the solution pK(A) value of the added base. We conclude that the pK(A) of Y(Z) is approximately 10.3 in D1-H190A PSII particles. In Mn-depleted wild-type PSII particles, P(680)()()(+) reduction was accelerated by all exogenous bases examined (substituted imidazoles, histidine, Tris, and 1,4-diazabicyclo[2.2.2]octane). We conclude that Y(Z) is solvent accessible in Mn-depleted wild-type PSII particles and that its pK(A) is near that of tyrosine in solution. In Mn-depleted wild-type PSII particles, over 80% of the kinetics of P(680)()()(+) reduction after a flash could be described by three kinetic components. The individual rate constants of these components varied slightly with pH, but their relative proportions varied dramatically with pH, showing apparent pK(A) values of 7.5 and 6.25 (6.9 and 5.8 in the presence of Ca(2+) and Mg(2+) ions). An additional pK(A) value (pK(A) < 4.5) may also be present. To describe these data, we propose (1) the pK(A) of His190 is 6.9-7.5, depending on buffer ions, (2) the deprotonation of Y(Z) is facilitated by the transient formation of a either a hydrogen bond or a hydrogen-bonded water bridge between Y(Z) and D1-His190, and (3) when protonated, D1-His190 interacts with nearby residues having pK(A) values near 6 and 4. Because Y(Z) and D1-His190 are located near the Mn cluster, these residues may interact with the Mn cluster in the intact system.
为了进一步阐明光系统II中D1-His190在酪氨酸Y(Z)氧化过程中的作用,我们测定了从蓝藻集胞藻PCC 6803分离得到的H190A和锰缺失野生型PSII颗粒中P(680)()()(+)还原的pH依赖性。测量在有和没有咪唑及其他小有机碱存在的情况下进行。在H190A PSII颗粒中,由于从Y(Z)进行电子转移导致的P(680)()()(+)的快速还原在pH 9以上显著增加,表观pK(A)约为10.3。在乙醇胺和咪唑存在的情况下,这种显著增加在较低的pH值时发生,Y(Z)氧化的效率与添加碱的溶液pK(A)值相关。我们得出结论,在D1-H190A PSII颗粒中Y(Z)的pK(A)约为10.3。在锰缺失野生型PSII颗粒中,所有检测的外源碱(取代咪唑、组氨酸、Tris和1,4-二氮杂双环[2.2.2]辛烷)都加速了P(680)()()(+)的还原。我们得出结论,在锰缺失野生型PSII颗粒中Y(Z)可与溶剂接触,并且其pK(A)接近溶液中酪氨酸的pK(A)。在锰缺失野生型PSII颗粒中,闪光后P(680)()()(+)还原动力学的80%以上可用三个动力学成分来描述。这些成分的各个速率常数随pH略有变化,但其相对比例随pH显著变化,表观pK(A)值为7.5和6.25(在Ca(2+)和Mg(2+)离子存在时为6.9和5.8)。也可能存在另一个pK(A)值(pK(A) < 4.5)。为了描述这些数据,我们提出:(1) His190的pK(A)为6.9 - 7.5,取决于缓冲离子;(2) Y(Z)的去质子化通过Y(Z)与D1-His190之间瞬时形成氢键或氢键水桥而得以促进;(3) 质子化时,D1-His190与pK(A)值接近6和4的附近残基相互作用。由于Y(Z)和D1-His190位于锰簇附近,这些残基在完整系统中可能与锰簇相互作用。