Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 345703
Title A simple artificial light-harvesting dyad as a model for excess energy dissipation on oxygenic photosynthesis
Author(s) Berera, R.; Herrero, C.; Stokkum, I.H.M. van; Vengris, M.; Kodis, G.; Palacios, R.E.; Amerongen, H. van; Grondelle, R. van; Gust, D.; Moore, T.A.; Moore, A.L.; Kennis, J.T.M.
Source Proceedings of the National Academy of Sciences of the United States of America 103 (2006)14. - ISSN 0027-8424 - p. 5343 - 5348.
Department(s) Biophysics
Publication type Refereed Article in a scientific journal
Publication year 2006
Keyword(s) excited singlet-state - green plants - chlorophyll fluorescence - xanthophyll cycle - photosystem-ii - s-1 state - carotenoids - complex - dynamics - antenna
Abstract Under excess illumination, plant photosystem II dissipates excess energy through the quenching of chlorophyll fluorescence, a process known as nonphotochemical quenching. Activation of nonphotochemical quenching has been linked to the conversion of a carotenoid with a conjugation length of nine double bonds (violaxanthin) into an 11-double-bond carotenoid (zeaxanthin). It has been suggested that the increase in the conjugation length turns the carotenoid from a nonquencher into a quencher of chlorophyll singlet excited states, but unequivocal evidence is lacking. Here, we present a transient absorption spectroscopic study on a model system made up of a zinc phthalocyanine (Pc) molecule covalently linked to carotenoids with 9, 10, or 11 conjugated carbon¿carbon double bonds. We show that a carotenoid can act as an acceptor of Pc excitation energy, thereby shortening its singlet excited-state lifetime. The conjugation length of the carotenoid is critical to the quenching process. Remarkably, the addition of only one double bond can turn the carotenoid from a nonquencher into a very strong quencher. By studying the solvent polarity dependence of the quenching using target analysis of the time-resolved data, we show that the quenching proceeds through energy transfer from the excited Pc to the optically forbidden S1 state of the carotenoid, coupled to an intramolecular charge-transfer state. The mechanism for excess energy dissipation in photosystem II is discussed in view of the insights obtained on this simple model system.
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