Guiles R D, Yachandra V K, McDermott A E, Cole J L, Dexheimer S L, Britt R D, Sauer K, Klein M P
Lawrence Berkeley Laboratory, Department of Chemistry, University of California, Berkeley 94720.
Biochemistry. 1990 Jan 16;29(2):486-96. doi: 10.1021/bi00454a024.
Hydroxylamine at low concentrations causes a two-flash delay in the first maximum flash yield of oxygen evolved from spinach photosystem II (PSII) subchloroplast membranes that have been excited by a series of saturating flashes of light. Untreated PSII membrane preparations exhibit a multiline EPR signal assigned to a manganese cluster and associated with the S2 state when illuminated at 195 K, or at 273 K in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU). We used the extent of suppression of the multiline EPR signal observed in samples illuminated at 195 K to determine the fraction of PSII reaction centers set back to a hydroxylamine-induced S0-like state, which we designate S0*. The manganese K-edge X-ray absorption edges for dark-adapted PSII preparations with or without hydroxylamine are virtually identical. This indicates that, despite its high binding affinity to the oxygen-evolving complex (OEC) in the dark, hydroxylamine does not reduce chemically the manganese cluster within the OEC in the dark. After a single turnover of PSII, a shift to lower energy is observed in the inflection of the Mn K-edge of the manganese cluster. We conclude that, in the presence of hydroxylamine, illumination causes a reduction of the OEC, resulting in a state resembling S0. This lower Mn K-edge energy of S0*, relative to the edge of S1, implies the storage and stabilization of an oxidative equivalent within the manganese cluster during the S0----S1 state transition. An analysis of the extended X-ray absorption fine structure (EXAFS) of the S0* state indicates that a significant structural rearrangement occurs between the S0* and S1 states. The X-ray absorption edge position and the structure of the manganese cluster in the S0* state are indicative of a heterogeneous mixture of formal valences of manganese including one Mn(II) which is not present in the S1 state.
低浓度的羟胺会使菠菜光系统II(PSII)亚叶绿体膜在一系列饱和闪光激发后,首次最大放氧量闪光产量出现双闪光延迟。未经处理的PSII膜制剂在195K光照下,或在273K且存在3-(3,4-二氯苯基)-1,1-二甲基脲(DCMU)的情况下,会表现出一种多线EPR信号,该信号归因于锰簇且与S2状态相关。我们利用在195K光照下样品中观察到的多线EPR信号的抑制程度,来确定PSII反应中心回到羟胺诱导的类似S0状态(我们称为S0*)的比例。有或没有羟胺的暗适应PSII制剂的锰K边X射线吸收边实际上是相同的。这表明,尽管羟胺在黑暗中对放氧复合体(OEC)具有高结合亲和力,但在黑暗中它不会化学还原OEC内的锰簇。PSII单次周转后,锰簇的Mn K边拐点出现向较低能量的移动。我们得出结论,在羟胺存在下,光照会导致OEC还原,从而产生类似S0的状态。相对于S1的边,S0的这种较低的Mn K边能量意味着在S0----S1状态转变过程中,氧化当量在锰簇内的储存和稳定。对S0状态的扩展X射线吸收精细结构(EXAFS)分析表明,S0和S1状态之间发生了显著的结构重排。S0状态下锰簇的X射线吸收边位置和结构表明,锰的形式价存在异质混合物,包括一个S1状态中不存在的Mn(II)。