Investigating Primary Charge Separation in the Reaction Center of Heliobacterium modesticaldum

2021 ◽  
Author(s):  
Moritz Brütting ◽  
Johannes M. Foerster ◽  
Stephan Kümmel
Keyword(s):  
Reaction Center ◽  
Charge Separation ◽  
Primary Charge Separation ◽  
Heliobacterium Modesticaldum

Primary Charge Separation and Energy Transfer in the Photosystem I Reaction Center of Higher Plants

1996 ◽  
Vol 100 (29) ◽  
pp. 12086-12099 ◽  
Author(s):  
Nigel T. H. White ◽  
Godfrey S. Beddard ◽  
Jonathan R. G. Thorne ◽  
Tim M. Feehan ◽  
Tia E. Keyes ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Reaction Center ◽  
Photosystem I ◽  
Charge Separation ◽  
Higher Plants ◽  
Primary Charge Separation

scholarly journals Temperature dependence of the photosynthetic primary charge separation : about photosystem I reaction center

2001 ◽  
Vol 41 (supplement) ◽  
pp. S71
Author(s):  
S. Kumazaki ◽  
I. Ikegami ◽  
K. Abiko ◽  
S. Yasuda ◽  
K. Yoshihara
Keyword(s):  
Temperature Dependence ◽  
Reaction Center ◽  
Photosystem I ◽  
Charge Separation ◽  
Primary Charge Separation

scholarly journals Switching sides—Reengineered primary charge separation in the bacterial photosynthetic reaction center

2019 ◽  
Vol 117 (2) ◽  
pp. 865-871 ◽  
Author(s):  
Philip D. Laible ◽  
Deborah K. Hanson ◽  
James C. Buhrmaster ◽  
Gregory A. Tira ◽  
Kaitlyn M. Faries ◽  
...  
Keyword(s):  
Reaction Center ◽  
Charge Separation ◽  
Internal Conversion ◽  
Photosynthetic Reaction Center ◽  
Primary Electron ◽  
Primary Electron Donor ◽  
Primary Charge Separation ◽  
Bacteriochlorophyll Dimer ◽  
Initial Charge ◽  
Bacterial Photosynthetic Reaction Center

We report 90% yield of electron transfer (ET) from the singlet excited state P* of the primary electron-donor P (a bacteriochlorophyll dimer) to the B-side bacteriopheophytin (HB) in the bacterial photosynthetic reaction center (RC). Starting from a platform Rhodobacter sphaeroides RC bearing several amino acid changes, an Arg in place of the native Leu at L185—positioned over one face of HB and only ∼4 Å from the 4 central nitrogens of the HB macrocycle—is the key additional mutation providing 90% yield of P+HB−. This all but matches the near-unity yield of A-side P+HA− charge separation in the native RC. The 90% yield of ET to HB derives from (minimally) 3 P* populations with distinct means of P* decay. In an ∼40% population, P* decays in ∼4 ps via a 2-step process involving a short-lived P+BB− intermediate, analogous to initial charge separation on the A side of wild-type RCs. In an ∼50% population, P* → P+HB− conversion takes place in ∼20 ps by a superexchange mechanism mediated by BB. An ∼10% population of P* decays in ∼150 ps largely by internal conversion. These results address the long-standing dichotomy of A- versus B-side initial charge separation in native RCs and have implications for the mechanism(s) and timescale of initial ET that are required to achieve a near-quantitative yield of unidirectional charge separation.

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