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运动性嗜盐杆菌膜中的二次电子转移过程。

Secondary electron transfer processes in membranes of Heliobacillus mobilis.

作者信息

Lin S, Chiou H C, Blankenship R E

机构信息

Department of Chemistry and Biochemistry, Arizona State University, Tempe 85287-1604, USA.

出版信息

Biochemistry. 1995 Oct 3;34(39):12761-7. doi: 10.1021/bi00039a036.

Abstract

Picosecond transient absorption difference spectroscopic experiments were performed on membranes of the antenna/reaction center complex of Heliobacillus mobilis to study the electron transfer processes. Particular emphasis was placed on the blue spectral region, where the difference spectra of iron-sulfur centers and quinones are significantly different. Spectra were measured at room temperature in the wavelength region from 400 to 470 nm and from 630 to 730 nm. Laser excitation was into the 788 nm Q gamma band of the bacteriochlorophyll g of the reaction center complex. Global analysis in both wavelength regions reveals three kinetic components. A 25 ps phase originates from the decay of the excited state of antenna to form the primary charge-separated state P798+A0-; a 600 ps component is assigned to the electron transfer from the primary electron acceptor A0 to a secondary electron acceptor; a nondecaying component on the time scale measured represents the formation of the secondary charge-separated state. When the secondary electron acceptors were reduced by adding dithionite at pH 11, the 600 ps component disappeared. Only a 25 ps component and a constant were observed in the 630-730 nm region. The 25 ps component is assigned to the excitation decay in the antenna and the formation of P798+A0-, just as in the nonreduced sample. In the reduced sample, the P798+A0- state does not decay on the time scale measured. In the 400-470 nm region, the same kinetic behavior was observed. The absorption difference spectra of the primary and the secondary electron acceptor were constructed from different charge-separated states.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对运动嗜盐杆菌的天线/反应中心复合物的膜进行了皮秒瞬态吸收差分光谱实验,以研究电子转移过程。特别关注了蓝色光谱区域,在该区域铁硫中心和醌的差分光谱有显著差异。在室温下,在400至470纳米以及630至730纳米的波长区域测量光谱。激光激发进入反应中心复合物细菌叶绿素g的788纳米Qγ带。两个波长区域的全局分析揭示了三个动力学成分。一个25皮秒的相源于天线激发态的衰减,形成初级电荷分离态P798 + A0 -;一个600皮秒的成分归因于从初级电子受体A0到次级电子受体的电子转移;在所测量的时间尺度上不衰减的成分代表次级电荷分离态的形成。当在pH 11下通过添加连二亚硫酸盐还原次级电子受体时,600皮秒的成分消失。在630 - 730纳米区域仅观察到一个25皮秒的成分和一个常数。25皮秒的成分归因于天线中的激发衰减和P798 + A0 -的形成,就像在未还原的样品中一样。在还原的样品中,P798 + A0 -态在所测量的时间尺度上不衰减。在400 - 470纳米区域也观察到了相同的动力学行为。从不同的电荷分离态构建了初级和次级电子受体的吸收差分光谱。(摘要截断于250字)

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