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对拟南芥中PsbR蛋白功能的见解。

Insights into the function of PsbR protein in Arabidopsis thaliana.

作者信息

Allahverdiyeva Yagut, Mamedov Fikret, Suorsa Marjaana, Styring Stenbjörn, Vass Imre, Aro Eva-Mari

机构信息

Department of Biology, Plant Physiology and Molecular Biology, University of Turku, FIN-20014 Turku, Finland.

出版信息

Biochim Biophys Acta. 2007 Jun;1767(6):677-85. doi: 10.1016/j.bbabio.2007.01.011. Epub 2007 Jan 25.

DOI:10.1016/j.bbabio.2007.01.011
PMID:17320041
Abstract

The functional state of the Photosystem (PS) II complex in Arabidopsis psbR T-DNA insertion mutant was studied. The DeltaPsbR thylakoids showed about 34% less oxygen evolution than WT, which correlates with the amounts of PSII estimated from Y(D)(ox) radical EPR signal. The increased time constant of the slow phase of flash fluorescence (FF)-relaxation and upshift in the peak position of the main TL-bands, both in the presence and in the absence of DCMU, confirmed that the S(2)Q(A)(-) and S(2)Q(B)(-) charge recombinations were stabilized in DeltaPsbR thylakoids. Furthermore, the higher amount of dark oxidized Cyt-b559 and the increased proportion of fluorescence, which did not decay during the 100s time span of the measurement thus indicating higher amount of Y(D)(+)Q(A)(-) recombination, pointed to the donor side modifications in DeltaPsbR. EPR measurements revealed that S(1)-to-S(2)-transition and S(2)-state multiline signal were not affected by mutation. The fast phase of the FF-relaxation in the absence of DCMU was significantly slowed down with concomitant decrease in the relative amplitude of this phase, indicating a modification in Q(A) to Q(B) electron transfer in DeltaPsbR thylakoids. It is concluded that the lack of the PsbR protein modifies both the donor and the acceptor side of the PSII complex.

摘要

对拟南芥psbR T-DNA插入突变体中光系统(PS)II复合体的功能状态进行了研究。DeltaPsbR类囊体的放氧量比野生型低约34%,这与从Y(D)(ox)自由基EPR信号估算的PSII含量相关。在有和没有敌草隆(DCMU)的情况下,闪光荧光(FF)弛豫慢相的时间常数增加以及主要TL带峰位上移,证实了DeltaPsbR类囊体中S(2)Q(A)(-)和S(2)Q(B)(-)电荷复合得到稳定。此外,在测量的100秒时间跨度内不衰减的暗氧化细胞色素b559含量较高以及荧光比例增加,表明Y(D)(+)Q(A)(-)复合量较高,这指向DeltaPsbR中供体侧的修饰。EPR测量表明,S(1)到S(2)的转变和S(2)态多线信号不受突变影响。在没有DCMU的情况下,FF弛豫的快相明显减慢,同时该相的相对振幅降低,表明DeltaPsbR类囊体中从Q(A)到Q(B)的电子传递发生了改变。得出的结论是,PsbR蛋白的缺失改变了PSII复合体的供体侧和受体侧。

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