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多种阴离子对叶绿体膜中光系统 II 的影响。

Multiple anion effects on photosystem II in chloroplast membranes.

机构信息

Department de Biologie, Service de Radioagronomie, Centre d'Etudes Nucléaires de Cadarache, F-13108, Saint-Paul-Lez-Durance, France.

出版信息

Photosynth Res. 1988 Jan;15(1):41-56. doi: 10.1007/BF00054987.

Abstract

We investigated the activity of several anions at various sites on photosystem II, in particular those associated with the Cl(-) effect (anion binding-site I) and the HCO3 (-) effect (anion binding-site II). Chlorophyll a fluorescence changes were used to monitor partial photosystem II reactions either in the oxygen-evolving mechanism or involving endogenous quinone electron acceptors. We find that anions such as NO3 (-), HCO3 (-), HCO2 (-), F(-), NO2 (-), and acetate can, depending on conditions, bind to either anion binding-site I, anion binding-site II, or both sites simultaneously. The anions N3 (-) and Au(CN)2 (-) are exceptions. In their presence, oxygen-consumption reactions are enhanced. The results demonstrate that an exclusive site or mode of action of an anion on photosystem II cannot be determined by measuring the Hill reaction alone. Anion interactions with photosystem II are shown to be very complex and, therefore, caution is advisable in interpreting related experiments. Carbonic anhydrase associated with photosystem II was also investigated as a possible target for some anion effects. In Cl(-)-depleted thylakoids, NO3 (-), stimulated both electron transport and carbonic anhydrase activity at low concentrations, while higher concentrations inhibited both. However, carbonic anhydrase was more sensitive to inhibition by NO3 (-) than was electron flow. Possible interpretations are discussed; the electron transport and carbonic anhydrase activity appear not to be functionally linked.

摘要

我们研究了几种阴离子在光系统 II 不同部位的活性,特别是那些与 Cl(-)效应(阴离子结合位点 I)和 HCO3 (-)效应(阴离子结合位点 II)相关的阴离子。叶绿素 a 荧光变化被用来监测部分光系统 II 反应,这些反应要么涉及氧释放机制,要么涉及内源性醌电子受体。我们发现,阴离子(如 NO3 (-)、HCO3 (-)、HCO2 (-)、F(-)、NO2 (-)和乙酸盐)可以根据条件,结合到阴离子结合位点 I、阴离子结合位点 II 或同时结合两个位点。N3 (-)和 Au(CN)2 (-)阴离子是例外。在它们的存在下,氧消耗反应增强。结果表明,不能仅通过测量希尔反应来确定阴离子在光系统 II 上的专属位点或作用模式。阴离子与光系统 II 的相互作用非常复杂,因此在解释相关实验时应谨慎。还研究了与光系统 II 相关的碳酸酐酶,以确定其是否可能是某些阴离子效应的靶标。在 Cl(-)耗尽的类囊体中,NO3 (-)在低浓度下刺激电子传递和碳酸酐酶活性,而高浓度则抑制两者。然而,碳酸酐酶对 NO3 (-)的抑制比电子传递更敏感。讨论了可能的解释;电子传递和碳酸酐酶活性似乎没有功能联系。

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