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Excitation Energy Transfer between Higher Excited States of Photosynthetic Pigments: 1. Carotenoids Intercept and Remove B Band Excitations

[Image: see text] Chlorophylls (Chls) are known for fast, subpicosecond internal conversion (IC) from ultraviolet/blue-absorbing (“B” or “Soret” states) to the energetically lower, red light-absorbing Q states. Consequently, excitation energy transfer (EET) in photosynthetic pigment–protein complexe...

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Detalles Bibliográficos
Autores principales: Götze, Jan P., Lokstein, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620780/
https://www.ncbi.nlm.nih.gov/pubmed/37929138
http://dx.doi.org/10.1021/acsomega.3c05895
Descripción
Sumario:[Image: see text] Chlorophylls (Chls) are known for fast, subpicosecond internal conversion (IC) from ultraviolet/blue-absorbing (“B” or “Soret” states) to the energetically lower, red light-absorbing Q states. Consequently, excitation energy transfer (EET) in photosynthetic pigment–protein complexes involving the B states has so far not been considered. We present, for the first time, a theoretical framework for the existence of B–B EET in tightly coupled Chl aggregates such as photosynthetic pigment–protein complexes. We show that according to a Förster resonance energy transport (FRET) scheme, unmodulated B–B EET has an unexpectedly high range. Unsuppressed, it could pose an existential threat: the damage potential of blue light for photochemical reaction centers (RCs) is well-known. This insight reveals so far undescribed roles for carotenoids (Crts, this article) and Chl b (next article in this series) of possibly vital importance. Our model system is the photosynthetic antenna pigment–protein complex (CP29). Here, we show that the B → Q IC is assisted by the optically allowed Crt state (S(2)): The sequence is B → S(2) (Crt, unrelaxed) → S(2) (Crt, relaxed) → Q. This sequence has the advantage of preventing ∼39% of Chl–Chl B–B EET since the Crt S(2) state is a highly efficient FRET acceptor. The B–B EET range and thus the likelihood of CP29 to forward potentially harmful B excitations toward the RC are thus reduced. In contrast to the B band of Chls, most Crt energy donation is energetically located near the Q band, which allows for 74/80% backdonation (from lutein/violaxanthin) to Chls. Neoxanthin, on the other hand, likely donates in the B band region of Chl b, with 76% efficiency. Crts thus act not only in their currently proposed photoprotective roles but also as a crucial building block for any system that could otherwise deliver harmful “blue” excitations to the RCs.