13C Chemical Shift Map of the Active Cofactors in Photosynthetic Reaction Centers ofRhodobacter sphaeroidesRevealed by Photo-CIDNP MAS NMR†

Biochemistry ◽  
2007 ◽  
Vol 46 (31) ◽  
pp. 8953-8960 ◽  
Author(s):  
Shipra Prakash ◽  
A. Alia ◽  
Peter Gast ◽  
Huub J. M. de Groot ◽  
Gunnar Jeschke ◽  
...  
2005 ◽  
Vol 127 (41) ◽  
pp. 14290-14298 ◽  
Author(s):  
Shipra Prakash ◽  
Alia ◽  
Peter Gast ◽  
Huub J. M. de Groot ◽  
Gunnar Jeschke ◽  
...  

Biochemistry ◽  
1997 ◽  
Vol 36 (24) ◽  
pp. 7513-7519 ◽  
Author(s):  
Tatjana A. Egorova-Zachernyuk ◽  
Barth van Rossum ◽  
Gert-Jan Boender ◽  
Eric Franken ◽  
Jennifer Ashurst ◽  
...  

2017 ◽  
Vol 231 (2) ◽  
Author(s):  
Jeremias C. Zill ◽  
Marcel Kansy ◽  
Reimund Goss ◽  
Lisa Köhler ◽  
A. Alia ◽  
...  

AbstractPhoto-CIDNP MAS NMR presents a unique tool to obtain insight into the photosynthetic reaction centers (RCs) of bacteria and plants. Using the dramatic enhancement of sensitivity and selectivity of the solid-state photo-CIDNP effect, structural as well as functional information can be obtained from the cofactor molecules forming a light-induced spin-correlated radical pair (SCRP) in a given reaction center. Here we demonstrate that the effect can be observed in a further species, which belongs neither to the plant nor the bacteria kingdom.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yin Song ◽  
Riley Sechrist ◽  
Hoang H. Nguyen ◽  
William Johnson ◽  
Darius Abramavicius ◽  
...  

AbstractPhotochemical reaction centers are the engines that drive photosynthesis. The reaction center from heliobacteria (HbRC) has been proposed to most closely resemble the common ancestor of photosynthetic reaction centers, motivating a detailed understanding of its structure-function relationship. The recent elucidation of the HbRC crystal structure motivates advanced spectroscopic studies of its excitonic structure and charge separation mechanism. We perform multispectral two-dimensional electronic spectroscopy of the HbRC and corresponding numerical simulations, resolving the electronic structure and testing and refining recent excitonic models. Through extensive examination of the kinetic data by lifetime density analysis and global target analysis, we reveal that charge separation proceeds via a single pathway in which the distinct A0 chlorophyll a pigment is the primary electron acceptor. In addition, we find strong delocalization of the charge separation intermediate. Our findings have general implications for the understanding of photosynthetic charge separation mechanisms, and how they might be tuned to achieve different functional goals.


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