Triplet Charge Recombination in Heliobacterial Reaction Centers Does Not Produce a Spin-Polarized EPR Spectrum

Author:

Ferlez Bryan1,Agostini Alessandro2,Carbonera Donatella2,Golbeck John H.34,van der Est Art45

Affiliation:

1. Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802, United States of America

2. Dipartimento di Scienze Chimiche, Università di Padova, Via Marzolo, 1, 35131 Padova, Italy

3. Department of Biochemistry and Molecular Biology and Department of Chemistry, The Pennsylvania State University, University Park, PA 16802, United States of America

4. Freiburg Institute of Advanced Studies (FRIAS), Albert-Ludwigs-Universität Freiburg, Albertstr.19, 79104 Freiburg, Germany

5. Departments of Chemistry and Physics, Brock University, 1812 Sir Isaac Brock Way, St. Catharines, ON, Canada L2S 3A1

Abstract

Abstract In photosynthetic reaction centers, reduction of the secondary acceptors leads to triplet charge recombination of the primary radical pair (RP). This process is spin selective and in a magnetic field it populates only the T0 state of the donor triplet state. As a result, the triplet state of the donor has a distinctive spin polarization pattern that can be measured by transient electron paramagnetic resonance (TREPR) spectroscopy. In heliobacterial reaction centers (HbRCs), the primary donor, P800, is composed of two bacteriochlorophyll g′ molecules and its triplet state has not been studied as extensively as those of other reaction centers. Here, we present TREPR and optically detected magnetic resonance (ODMR) data of 3P800 and show that although it can be detected by ODMR it is not observed in the TREPR data. We demonstrate that the absence of the TREPR spectrum is a result of the fact that the zero-field splitting (ZFS) tensor of 3P800 is maximally rhombic, which results in complete cancelation of the absorptive and emissive polarization in randomly oriented samples.

Publisher

Walter de Gruyter GmbH

Subject

Physical and Theoretical Chemistry

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