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叶绿素a和叶绿素d对于蓝细菌海栖热袍菌光系统II中的光化学过程均至关重要。

Both chlorophylls a and d are essential for the photochemistry in photosystem II of the cyanobacteria, Acaryochloris marina.

作者信息

Schlodder Eberhard, Cetin Marianne, Eckert Hann-Jörg, Schmitt Franz-Josef, Barber James, Telfer Alison

机构信息

Max-Volmer-Laboratorium für Biophysikalische Chemie, Technische Universität Berlin, Strasse des 17.Juni 135, 10623 Berlin, Germany.

出版信息

Biochim Biophys Acta. 2007 Jun;1767(6):589-95. doi: 10.1016/j.bbabio.2007.02.018. Epub 2007 Mar 3.

Abstract

We have measured the flash-induced absorbance difference spectrum attributed to the formation of the secondary radical pair, P(+)Q(-), between 270 nm and 1000 nm at 77 K in photosystem II of the chlorophyll d containing cyanobacterium, Acaryochloris marina. Despite the high level of chlorophyll d present, the flash-induced absorption difference spectrum of an approximately 2 ms decay component shows a number of features which are typical of the difference spectrum seen in oxygenic photosynthetic organisms containing no chlorophyll d. The spectral shape in the near-UV indicates that a plastoquinone is the secondary acceptor molecule (Q(A)). The strong C-550 change at 543 nm confirms previous reports that pheophytin a is the primary electron acceptor. The bleach at 435 nm and increase in absorption at 820 nm indicates that the positive charge is stabilized on a chlorophyll a molecule. In addition a strong electrochromic band shift, centred at 723 nm, has been observed. It is assigned to a shift of the Qy band of the neighbouring accessory chlorophyll d, Chl(D1). It seems highly likely that it accepts excitation energy from the chlorophyll d containing antenna. We therefore propose that primary charge separation is initiated from this chlorophyll d molecule and functions as the primary electron donor. Despite its lower excited state energy (0.1 V less), as compared to chlorophyll a, this chlorophyll d molecule is capable of driving the plastoquinone oxidoreductase activity of photosystem II. However, chlorophyll a is used to stabilize the positive charge and ultimately to drive water oxidation.

摘要

我们在含有叶绿素d的蓝细菌——滨海红藻的光系统II中,于77 K下测量了归因于次级自由基对P(+)Q(-)形成的闪光诱导吸光度差光谱,测量范围为270 nm至1000 nm。尽管存在高水平的叶绿素d,但一个约2 ms衰减成分的闪光诱导吸收差光谱显示出许多特征,这些特征是不含叶绿素d的产氧光合生物中所见差光谱的典型特征。近紫外区域的光谱形状表明,质体醌是次级受体分子(Q(A))。543 nm处强烈的C-550变化证实了先前的报道,即脱镁叶绿素a是初级电子受体。435 nm处的漂白和820 nm处吸收的增加表明正电荷稳定在叶绿素a分子上。此外,还观察到一个以723 nm为中心的强电致变色带位移。它被归因于相邻辅助叶绿素d(Chl(D1))的Qy带的位移。它似乎极有可能从含叶绿素d的天线接受激发能。因此,我们提出初级电荷分离从这个叶绿素d分子开始,并作为初级电子供体起作用。尽管与叶绿素a相比,其激发态能量较低(低0.1 V),但这个叶绿素d分子能够驱动光系统II的质体醌氧化还原酶活性。然而,叶绿素a用于稳定正电荷并最终驱动水氧化。

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