The reduced S-1 and S-2 oxidation states of the O2-evolving complex of photosystem II: An EPR microwave power saturation study

1Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Progressive microwave power saturation (P1/2) measurements have been performed on the tyrosine D radical (YD•) of photosystem II (PSII) in order to examine its relaxation enhancement by the oxygen-evolving complex (OEC) poised to the reduced S-1 and S-2 oxidation states by NO treatment. Analysis of the power saturation curves showed that the S-1 oxidation state of the OEC does not enhance the relaxation of YD•: it therefore possesses a diamagnetic ground state. In contrast, the Mn(II)-Mn(III) multiline electron paramagnetic resonance (EPR) signal characteristic of the S-2 oxidation state of the OEC was shown to provide a relaxation enhancement pathway for YD•, however less efficient relative to the one provided by the S2-state multiline EPR signal. We also examined the YD• relaxation enhancement characteristics of the EPR-silent oxidation state produced after brief (1-5 min) dark incubation at 0°C of a PSII sample poised to the EPRactive S-2 state. This EPR-silent oxidation state denoted as "0°C incubation" state was shown to possess remarkably similar P1/2 values with the EPR-active S-2 state in the overall examined temperature range (6-20 K). In addition, these values remained unchanged after successive cycles of the OEC between the EPR-active S-2 state and the "0°C incubation" state. The data presented in this work point to the conclusion that the "0°C incubation" state is indeed an S-2 oxidation state with half-integer spin. © Springer Science+Business Media B.V. 2010.

Cite

CITATION STYLE

APA

Koulougliotis, D. (2009). The reduced S-1 and S-2 oxidation states of the O2-evolving complex of photosystem II: An EPR microwave power saturation study. Photosynthetica, 47(4), 567–574. https://doi.org/10.1007/s11099-009-0082-8

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free