Department of Chemistry, Institute for Biophysical Dynamics, and The James Franck Institute, The University of Chicago, Chicago, Illinois 60637, USA.
Graduate Program in the Biophysical Sciences, Institute for Biophysical Dynamics, and The James Franck Institute, The University of Chicago, Chicago, Illinois 60637, USA.
J Chem Phys. 2017 Oct 7;147(13):131101. doi: 10.1063/1.4999057.
In photosynthetic organisms, the pigment-protein complexes that comprise the light-harvesting antenna exhibit complex electronic structures and ultrafast dynamics due to the coupling among the chromophores. Here, we present absorptive two-dimensional (2D) electronic spectra from living cultures of the purple bacterium, Rhodobacter sphaeroides, acquired using gradient assisted photon echo spectroscopy. Diagonal slices through the 2D lineshape of the LH1 stimulated emission/ground state bleach feature reveal a resolvable higher energy population within the B875 manifold. The waiting time evolution of diagonal, horizontal, and vertical slices through the 2D lineshape shows a sub-100 fs intra-complex relaxation as this higher energy population red shifts. The absorption (855 nm) of this higher lying sub-population of B875 before it has red shifted optimizes spectral overlap between the LH1 B875 band and the B850 band of LH2. Access to an energetically broad distribution of excitonic states within B875 offers a mechanism for efficient energy transfer from LH2 to LH1 during photosynthesis while limiting back transfer. Two-dimensional lineshapes reveal a rapid decay in the ground-state bleach/stimulated emission of B875. This signal, identified as a decrease in the dipole strength of a strong transition in LH1 on the red side of the B875 band, is assigned to the rapid localization of an initially delocalized exciton state, a dephasing process that frustrates back transfer from LH1 to LH2.
在光合生物中,组成光捕获天线的色素-蛋白复合物由于发色团之间的耦合而具有复杂的电子结构和超快动力学。在这里,我们使用梯度辅助光子回波光谱学从生活在培养的红细菌 Rhodobacter sphaeroides 中获得了吸收性二维(2D)电子光谱。通过 LH1 受激发射/基态漂白特征的二维线形状的对角切片揭示了 B875 分子中可分辨的更高能量群体。对角、水平和垂直切片通过二维线形状的等待时间演化表明,由于更高能量群体的红移,在 100fs 以内发生了复合物内松弛。在 B875 发生红移之前吸收(855nm)这个更高的 B875 子群体优化了 LH1 B875 带和 LH2 的 B850 带之间的光谱重叠。在 B875 中获得广泛的激子态能量分布提供了在光合作用期间从 LH2 到 LH1 有效能量转移的机制,同时限制了反向转移。二维线形状揭示了 B875 的基态漂白/受激发射的快速衰减。这个信号被确定为 B875 带的红侧的 LH1 中强跃迁的偶极子强度的降低,被分配给最初离域的激子态的快速定位,这是一种去相位过程,它阻碍了从 LH1 到 LH2 的反向转移。