Flanagan Moira L, Long Phillip D, Dahlberg Peter D, Rolczynski Brian S, Massey Sara C, Engel Gregory S
Department of Chemistry, The James Franck Institute and The Institute for Biophysical Dynamics, The University of Chicago , Chicago, Illinois 60637, United States.
J Phys Chem A. 2016 Mar 10;120(9):1479-87. doi: 10.1021/acs.jpca.5b08366. Epub 2015 Dec 16.
The bacterial reaction center is capable of both efficiently collecting and quickly transferring energy within the complex; therefore, the reaction center serves as a convenient model for both energy transfer and charge separation. To spectroscopically probe the interactions between the electronic excited states on the chromophores and their intricate relationship with vibrational motions in their environment, we examine coherences between the excited states. Here, we investigate this question by introducing a series of point mutations within 12 Å of the special pair of bacteriochlorophylls in the Rhodobacter sphaeroides reaction center. Using two-dimensional spectroscopy, we find that the time scales of energy transfer dynamics remain unperturbed by these mutations. However, within these spectra, we detect changes in the mixed vibrational-electronic coherences in these reaction centers. Our results indicate that resonance between bacteriochlorophyll vibrational modes and excitonic energy gaps promote electronic coherences and support current vibronic models of photosynthetic energy transfer.
细菌反应中心能够在复合物内部高效收集并快速转移能量;因此,反应中心成为研究能量转移和电荷分离的便捷模型。为了通过光谱学方法探究发色团上电子激发态之间的相互作用及其与周围环境中振动运动的复杂关系,我们研究了激发态之间的相干性。在此,我们通过在球形红细菌反应中心特殊对的细菌叶绿素12 Å范围内引入一系列点突变来研究这个问题。利用二维光谱,我们发现能量转移动力学的时间尺度不受这些突变的影响。然而,在这些光谱中,我们检测到这些反应中心中混合振动 - 电子相干性的变化。我们的结果表明,细菌叶绿素振动模式与激子能隙之间的共振促进了电子相干性,并支持了当前光合作用能量转移的振动电子模型。