镧系元素抑制光系统 II 氧生成复合物的机制

IF 4.033 Q4 Biochemistry, Genetics and Molecular Biology
E. R. Lovyagina, A. V. Loktyushkin, N. S. Vasiliev, B. K. Semin
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引用次数: 0

摘要

摘要本文研究了La3+和Tb3+阳离子与光系统II贫钙样品的析氧复合物钙结合位点的相互作用。阳离子与ca结合位点的结合是不可逆的,结合的阳离子不能被冲走或被Ca2+阳离子取代。利用镧系元素与ca结合位点的强结合特性,研究了结合的Ln3+阳离子是否对氧络合物的高亲和力mn结合位点有影响。为此,使用对苯二酚从钙耗尽光系统II膜的氧络合物中提取锰阳离子,钙结合位点被La3+或Tb3+阻断,然后使用外源电子供体(Mn2+ + H2O2)和1,5-二苯基卡巴肼检测高亲和力位点的活性。发现镧系离子结合到ca结合位点,通过高亲和力的mn结合位点显著抑制电子给体的氧化。讨论了观察到的效应的机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanism of Inhibition of the Oxygen-Evolving Complex of Photosystem II by Lanthanide Cations

Mechanism of Inhibition of the Oxygen-Evolving Complex of Photosystem II by Lanthanide Cations

Mechanism of Inhibition of the Oxygen-Evolving Complex of Photosystem II by Lanthanide Cations

The interaction of La3+ and Tb3+ cations with the Ca-binding site of the oxygen-evolving complex of photosystem II samples depleted of calcium has been studied. The binding of cations to the Ca-binding site is irreversible and the bound cations cannot be washed out or replaced by Ca2+ cations. The feature of lanthanides to bind strongly to the Ca-binding site was used to investigate whether the bound Ln3+ cation has an effect on the high-affinity Mn-binding site of the oxygen-evolving complex. For this purpose, hydroquinone was used to extract manganese cations from the oxygen-evolving complex of the calcium-depleted photosystem II membranes with the Ca-binding site blocked by La3+ or Tb3+, and the activity of the high-affinity site was then examined using exogenous electron donors (Mn2+ + H2O2) and 1,5-diphenylcarbazide. It was found that lanthanide cations bound to the Ca-binding site significantly inhibited oxidation of electron donors through the high-affinity Mn-binding site. The mechanism of the observed effect is discussed.

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来源期刊
Biophysics
Biophysics Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
1.20
自引率
0.00%
发文量
67
期刊介绍: Biophysics is a multidisciplinary international peer reviewed journal that covers a wide scope of problems related to the main physical mechanisms of processes taking place at different organization levels in biosystems. It includes structure and dynamics of macromolecules, cells and tissues; the influence of environment; energy transformation and transfer; thermodynamics; biological motility; population dynamics and cell differentiation modeling; biomechanics and tissue rheology; nonlinear phenomena, mathematical and cybernetics modeling of complex systems; and computational biology. The journal publishes short communications devoted and review articles.
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