Angerhofer A, Bornhäuser F, Aust V, Hartwich G, Scheer H
Department of Chemistry, University of Florida, Gainesville, FL 32611, USA
Biochim Biophys Acta. 1998 Jul 20;1365(3):404-420. doi: 10.1016/s0005-2728(98)00093-0.
[3-vinyl]-132-OH-bacteriochlorophyll a has been selectively exchanged against native bacteriochlorophyll a in the monomer binding sites at the A- and B-branch of the photosynthetic reaction centre from Rhodobacter sphaeroides. Transient absorption difference measurements were performed on these samples over a temperature range from 4.2 to 300 K with 20 ns time resolution. Specifically the decay of the primary donor triplet state, 3P870, as well as the rise and decay rates of the carotenoid triplet state, 3Car (spheroidene), were measured. The observed rates revealed a thermally activated carotenoid triplet formation corresponding to the decay of the primary donor triplet state. The activation energies for the triplet energy transfer process were 100(+/-10) cm-1 for reaction centers from wild-type Rhodobacter sphaeroides 2.4.1, with and without exchange of the monomeric bacteriochlorophyll on the electron transfer-active branch, BA. For reaction centers from Rhodobacter sphaeroides R26.1 with both monomers exchanged against [3-vinyl]-132-OH-bacteriochlorophyll a, and subsequent spheroidene reconstitution the activation energy was 460(+/-20) cm-1. These activation energies correspond to the energy difference between the triplet states of the accessory BChl monomer, BB, and the primary donor when native BChl a or [3-vinyl]-132-OH-BChl a is present in the BB binding site. In all samples the 3Car formation rates were bi-phasic over a large temperature range. A fast temperature-independent rate was observed on the wavelength of the carotenoid triplet-triplet absorption which dominated at very low temperatures. Additionally, a slower temperature-independent 3Car formation rate was observed at low temperatures which could be explained with the assumption of heterogeneity in the energy barrier (3BB) and/or the primary donor triplet state (3P870). A tunneling mechanism as proposed earlier by Kolaczkowski (PhD thesis, Brown University, 1989) is not only unnecessary but also incompatible with the available experimental data.
[3 - 乙烯基]-132 - 羟基细菌叶绿素a已在球形红细菌光合反应中心A分支和B分支的单体结合位点上与天然细菌叶绿素a进行了选择性交换。在4.2至300 K的温度范围内,以20 ns的时间分辨率对这些样品进行了瞬态吸收差异测量。具体测量了初级供体三重态3P870的衰减以及类胡萝卜素三重态3Car(球形烯)的上升和衰减速率。观察到的速率揭示了与初级供体三重态衰减相对应的热激活类胡萝卜素三重态形成。对于野生型球形红细菌2.4.1的反应中心,无论电子转移活性分支BA上的单体细菌叶绿素是否交换,三重态能量转移过程的活化能均为100(±10)cm-1。对于球形红细菌R26.1的反应中心,两个单体都被[3 - 乙烯基]-132 - 羟基细菌叶绿素a交换,随后进行球形烯重构,活化能为460(±20)cm-1。这些活化能对应于当天然细菌叶绿素a或[3 - 乙烯基]-132 - 羟基细菌叶绿素a存在于BB结合位点时,辅助BChl单体BB和初级供体的三重态之间的能量差。在所有样品中,3Car形成速率在很大的温度范围内呈双相。在类胡萝卜素三重态 - 三重态吸收波长处观察到一个快速的与温度无关的速率,该速率在非常低的温度下占主导。此外,在低温下观察到一个较慢的与温度无关的3Car形成速率,这可以通过能量势垒(3BB)和/或初级供体三重态(3P870)的异质性假设来解释。Kolaczkowski(博士论文,布朗大学,1989年)早些时候提出的隧穿机制不仅不必要,而且与现有实验数据不兼容。