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Asymmetric Electron Transfer in Cyanobacterial Photosystem I: Charge Separation and Secondary Electron Transfer Dynamics of Mutations Near the Primary Electron Acceptor A0

机译:蓝细菌光系统中的不对称电子转移I:主电子受体A0附近的电荷分离和次级电子转移动力学

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摘要

Point mutations were introduced near the primary electron acceptor sites assigned to A0 in both the PsaA and PsaB branches of Photosystem I in the cyanobacterium Synechocystis sp. PCC 6803. The residues Met688PsaA and Met668PsaB, which provide the axial ligands to the Mg2+ of the eC-A3 and eC-B3 chlorophylls, were changed to leucine and asparagine (chlorophyll notation follows Jordan et al., 2001). The removal of the ligand is expected to alter the midpoint potential of the \documentclass[12pt]{minimal}\usepackage{amsmath}\usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy}\usepackage{mathrsfs}\setlength{\oddsidemargin}{-69pt}\begin{document}\begin{equation*}{\mathrm{A}}_{0}/{\mathrm{A}}_{0}^{-}\end{equation*}\end{document} redox pair and result in a change in the intrinsic charge separation rate and secondary electron transfer kinetics from \documentclass[12pt]{minimal}\usepackage{amsmath}\usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy}\usepackage{mathrsfs}\setlength{\oddsidemargin}{-69pt}\begin{document}\begin{equation*}{\mathrm{A}}_{0}^{-}\end{equation*}\end{document} to A1. The dynamics of primary charge separation and secondary electron transfer were studied at 690 nm and 390 nm in these mutants by ultrafast optical pump-probe spectroscopy. The data reveal that mutations in the PsaB branch do not alter electron transfer dynamics, whereas mutations in the PsaA branch have a distinct effect on electron transfer, slowing down both the primary charge separation and the secondary electron transfer step (the latter by a factor of 3–10). These results suggest that electron transfer in cyanobacterial Photosystem I is asymmetric and occurs primarily along the PsaA branch of cofactors.
机译:将点突变引入到蓝藻集胞藻属(Sychochocystis sp)的光系统I的PsaA和PsaB分支中分配给A0的主要电子受体位点附近。 PCC 6803.为eC-A3和eC-B3叶绿素的Mg2 +提供轴向配体的残基Met688PsaA和Met668PsaB变为亮氨酸和天冬酰胺(叶绿素​​标记遵循Jordan等人,2001年)。预期去除配体会改变\ documentclass [12pt] {minimum} \ usepackage {amsmath} \ usepackage {wasysym} \ usepackage {amsfonts} \ usepackage {amssymb} \ usepackage {amsbsy} \ usepackage { mathrsfs} \ setlength {\ oddsidemargin} {-69pt} \ begin {document} \ begin {equation *} {\ mathrm {A}} _ {0} / {\ mathrm {A}} _ {0} ^ {-} \ end {equation *} \ end {document}氧化还原对,导致本征电荷分离率和二次电子转移动力学从\ documentclass [12pt] {minimum} \ usepackage {amsmath} \ usepackage {wasysym} \ usepackage改变{amsfonts} \ usepackage {amssymb} \ usepackage {amsbsy} \ usepackage {mathrsfs} \ setlength {\ oddsidemargin} {-69pt} \ begin {document} \ begin {equation *} {\ mathrm {A}} _ {0} ^ {-} \ end {equation *} \ end {document}到A1。通过超快光学泵浦探针光谱法研究了这些突变体在690 nm和390 nm处的一次电荷分离和二次电子转移的动力学。数据显示,PsaB分支中的突变不会改变电子转移动力学,而PsaA分支中的突变对电子转移有明显影响,从而减慢了主电荷分离和次级电子转移步骤的速度(后者降低了两倍)。 3-10)。这些结果表明,在蓝细菌光系统I中,电子转移是不对称的,主要发生在辅因子的PsaA分支上。

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