| Literature DB >> 25054941 |
Franklin D Fuller1, Jie Pan1, Andrius Gelzinis2, Vytautas Butkus2, S Seckin Senlik1, Daniel E Wilcox1, Charles F Yocum3, Leonas Valkunas2, Darius Abramavicius4, Jennifer P Ogilvie1.
Abstract
Photosynthesis powers life on our planet. The basic photosynthetic architecture consists of antenna complexes that harvest solar energy and reaction centres that convert the energy into stable separated charge. In oxygenic photosynthesis, the initial charge separation occurs in the photosystem II reaction centre, the only known natural enzyme that uses solar energy to split water. Both energy transfer and charge separation in photosynthesis are rapid events with high quantum efficiencies. In recent nonlinear spectroscopic experiments, long-lived coherences have been observed in photosynthetic antenna complexes, and theoretical work suggests that they reflect underlying electronic-vibrational resonances, which may play a functional role in enhancing energy transfer. Here, we report the observation of coherent dynamics persisting on a picosecond timescale at 77 K in the photosystem II reaction centre using two-dimensional electronic spectroscopy. Supporting simulations suggest that the coherences are of a mixed electronic-vibrational (vibronic) nature and may enhance the rate of charge separation in oxygenic photosynthesis.Entities:
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Year: 2014 PMID: 25054941 DOI: 10.1038/nchem.2005
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427