Publisher’s Note: “Investigation of water bound to photosystem I with multiquantum filtered O17 nuclear magnetic resonance” [J. Chem. Phys. 128, 014503 (2008)]

2008 ◽  
Vol 128 (11) ◽  
pp. 119902
Author(s):  
M. Krzystyniak ◽  
Gaozhong Shen ◽  
John H. Golbeck ◽  
Mikhail L. Antonkine
2019 ◽  
Vol 517 ◽  
pp. 273
Author(s):  
G.V. Mozzhukhin ◽  
G.S. Kupriyanova ◽  
S.Sh. Mamadazizov ◽  
A. Maraşlı ◽  
B.Z. Rameev

2020 ◽  
Vol 1 (2) ◽  
pp. 261-274
Author(s):  
Geertje J. Janssen ◽  
Patrick Eschenbach ◽  
Patrick Kurle ◽  
Bela E. Bode ◽  
Johannes Neugebauer ◽  
...  

Abstract. The electron donor in photosystem I (PSI), the chlorophyll dimer P700, is studied by photochemically induced dynamic nuclear polarization (photo-CIDNP) magic angle spinning (MAS) nuclear magnetic resonance (NMR) on selectively 13C and uniformly 15N labeled PSI core preparations (PSI-100) obtained from the aquatic plant duckweed (Spirodela oligorrhiza). Light-induced signals originate from the isotope-labeled nuclei of the cofactors involved in the spin-correlated radical pair forming upon light excitation. Signals are assigned to the two donor cofactors (Chl a and Chl a') and the two acceptor cofactors (both Chl a). Light-induced signals originating from both donor and acceptor cofactors demonstrate that electron transfer occurs through both branches of cofactors in the pseudo-C2 symmetric reaction center (RC). The experimental results supported by quantum chemical calculations indicate that this functional symmetry occurs in PSI despite similarly sized chemical shift differences between the cofactors of PSI and the functionally asymmetric special pair donor of the bacterial RC of Rhodobacter sphaeroides. This contributes to converging evidence that local differences in time-averaged electronic ground-state properties, over the donor are of little importance for the functional symmetry breaking across photosynthetic RC species.


2008 ◽  
Vol 128 (1) ◽  
pp. 014503 ◽  
Author(s):  
M. Krzystyniak ◽  
Gaozhong Shen ◽  
John H. Golbeck ◽  
Mikhail L. Antonkine

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