Lin S, Chiou H C, Kleinherenbrink F A, Blankenship R E
Department of Chemistry and Biochemistry, Arizona State University, Tempe 85287-1604.
Biophys J. 1994 Feb;66(2 Pt 1):437-45. doi: 10.1016/s0006-3495(94)80794-5.
The kinetics of excitation energy transfer and electron transfer processes within the membrane of Heliobacillus mobilis were investigated using femtosecond transient absorption difference spectroscopy at room temperature. The kinetics in the 725- to 865-nm region, upon excitation at 590 and 670 nm, were fit using global analysis. The fits returned three kinetic components with lifetimes of 1-2 ps and 27-30 ps, and a component that does not decay within several nanoseconds. The 1- to 2-ps component is attributed to excitation equilibration to form a thermally relaxed excited state. The 27- to 30-ps phase corresponds to the decay of the relaxed excited state to form a charge-separated state. The intrinsic energy and electron transfer rates were estimated using the experimental results and theoretical models for excitation migration and trapping dynamics. Taking into account the number of antenna pigments and their spectral distribution, an upper limit of 1.2 ps for the intrinsic time constant for charge separation in the reaction center is calculated. This upper limit corresponds with the trapping-limited case for excitation migration and trapping. Reduction of the primary electron acceptor A0 was observed in the 640 to 700 nm region using excitation at 780 nm. An instantaneous absorbance increase followed by a decay of about 30 ps was observed over a broad wavelength region due to the excited state absorption and decay of BChl g molecules in the antenna. In addition, a narrow bleaching band centered at 670 nm grows in with an apparent time constant of about 1.0 ps, superimposed on the 30-ps absorbance increase due to excited state absorption. Measurements on a longer time scale showed that besides the 670 nm pigment a BChl g molecule absorbing near 785 nm may be involved in the primary charge separation, and that this pigment may be in equilibrium with the 670 nm pigment. The bleaching bands at 670 nm and 785nm recovered with a time constant of about 600 ps, due to forward electron transport to a secondary electron acceptor. Energy and electron transfer properties of H. mobilis membranes are compared with Photosystem 1, to which the heliobacteria bear an evolutionary relationship.
在室温下,使用飞秒瞬态吸收差分光谱研究了运动嗜盐杆菌膜内激发能转移和电子转移过程的动力学。在590和670nm激发下,对725至865nm区域的动力学进行了全局分析拟合。拟合得到三个动力学成分,寿命分别为1 - 2ps和27 - 30ps,以及一个在几纳秒内不衰减的成分。1至2ps的成分归因于激发平衡以形成热弛豫激发态。27至30ps的阶段对应于弛豫激发态的衰减以形成电荷分离态。利用激发迁移和俘获动力学的实验结果和理论模型估计了本征能量和电子转移速率。考虑到天线色素的数量及其光谱分布,计算出反应中心电荷分离本征时间常数的上限为1.2ps。该上限对应于激发迁移和俘获的俘获限制情况。在780nm激发下,在640至700nm区域观察到初级电子受体A0的还原。由于天线中BChl g分子的激发态吸收和衰减,在宽波长区域观察到瞬时吸光度增加,随后约30ps衰减。此外,以约1.0ps的表观时间常数出现一个以670nm为中心的窄漂白带,叠加在由于激发态吸收导致的30ps吸光度增加上。在更长时间尺度上的测量表明,除了670nm色素外,在785nm附近吸收的BChl g分子可能参与初级电荷分离,并且该色素可能与670nm色素处于平衡状态。由于向前电子传输到次级电子受体,670nm和785nm处的漂白带以约600ps的时间常数恢复。将运动嗜盐杆菌膜的能量和电子转移特性与光合系统1进行了比较,嗜盐杆菌与光合系统1具有进化关系。