EPR was used to study the influence of formate on the electron acceptor side of photosystem II (PSII) from Thermosynechococcus elongatus. Two new EPR signals were found and characterized. The first is assigned to the semiquinone form of Q(B) interacting magnetically with a high spin, non-heme-iron (Fe2+, S=2) when the native bicarbonate/carbonate ligand is replaced by formate. This assignment is based on several experimental observations, the most important of which were: (i) its presence in the dark in a significant fraction of centers, and (ii) the period-of-two variations in the concentration expected for QB(center dot-) when PSII underwent a series of single-electron turnovers. This signal is similar but not identical to the well-know f...
AbstractEPR signals in the high-spin region were studied at 10 K in photosystem II (PS II) particles...
AbstractPhotosystem 2 preparations with very high rates of oxygen evolution from the thermophilic cy...
The bacteria Rhodobacter sphaeroides uses photosynthetic reaction centers to convert light into chem...
EPR was used to study the influence of formate on the electron acceptor side of photosystem II (PSII...
AbstractEPR was used to study the influence of formate on the electron acceptor side of photosystem ...
The semiquinone-iron complex of photosystem II was studied using electron spin resonance (ESR) spect...
AbstractWe have investigated the quinone-binding region of PS II using exchange reactions to replace...
Formate is known to cause significant inhibition in the electron and proton transfers in photosystem...
AbstractFormate is known to cause significant inhibition in the electron and proton transfers in pho...
Photosystem II (PSII) uses light energy to oxidise water and reduce quinone. The water oxidation sit...
AbstractThe EPR signal of the iron-quinone electron acceptor of photosystem II in higher plant chlor...
AbstractThe EPR signal of the iron-quinone electron acceptor of photosystem II in higher plant chlor...
AbstractEPR signals in the high-spin region were studied at 10 K in photosystem II (PS II) particles...
Le photosystème II (PSII) est un complexe multi-protéique qui utilise l'énergie solaire pour oxyder ...
In photosynthetic bacteria, light-induced electron transfer takes place in a protein called the reac...
AbstractEPR signals in the high-spin region were studied at 10 K in photosystem II (PS II) particles...
AbstractPhotosystem 2 preparations with very high rates of oxygen evolution from the thermophilic cy...
The bacteria Rhodobacter sphaeroides uses photosynthetic reaction centers to convert light into chem...
EPR was used to study the influence of formate on the electron acceptor side of photosystem II (PSII...
AbstractEPR was used to study the influence of formate on the electron acceptor side of photosystem ...
The semiquinone-iron complex of photosystem II was studied using electron spin resonance (ESR) spect...
AbstractWe have investigated the quinone-binding region of PS II using exchange reactions to replace...
Formate is known to cause significant inhibition in the electron and proton transfers in photosystem...
AbstractFormate is known to cause significant inhibition in the electron and proton transfers in pho...
Photosystem II (PSII) uses light energy to oxidise water and reduce quinone. The water oxidation sit...
AbstractThe EPR signal of the iron-quinone electron acceptor of photosystem II in higher plant chlor...
AbstractThe EPR signal of the iron-quinone electron acceptor of photosystem II in higher plant chlor...
AbstractEPR signals in the high-spin region were studied at 10 K in photosystem II (PS II) particles...
Le photosystème II (PSII) est un complexe multi-protéique qui utilise l'énergie solaire pour oxyder ...
In photosynthetic bacteria, light-induced electron transfer takes place in a protein called the reac...
AbstractEPR signals in the high-spin region were studied at 10 K in photosystem II (PS II) particles...
AbstractPhotosystem 2 preparations with very high rates of oxygen evolution from the thermophilic cy...
The bacteria Rhodobacter sphaeroides uses photosynthetic reaction centers to convert light into chem...