Light harvesting and photoprotective states in the marine diatom Fragilariopsis sp.: functional implications of chlorophylls c1/c2 in the fucoxanthin-chlorophyll a/c-binding proteins (FCPs)

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Abstract

We report pH/pD-dependent fluorescence-excitation spectra of the light-harvesting fucoxanthin-chlorophyll a/c-binding proteins (FCPs) of the marine diatom Fragilariopsis sp. There is a reversible 451 to 455 nm Soret transition accompanied by a 588 to 586 nm Qx transition of chlorophylls c1/c2 in the pH/pD 4.9-8 range with a pKa = 5.4. The H/D exchangeable site of the 17-acrylate group of chlorophylls c1/c2 was characterized and from the pH/pD sensitivity of the Soret and Qy bands we suggest that the chlorophylls c1/c2-acrylate-H2O moiety can act as a proton acceptor/donor site. Under high intensity light conditions, the acrylate moiety of chlorophylls c1/c2 becomes protonated, resembling that observes under acidic conditions. In the photoprotective state, the absorption of chlorophylls c1/c2 is red shifted and resembles that observed in the reversible transition from light-harvesting to energy-quenching state at acidic pH. The induced ΔpH and that created from the high intensity light, is responsible for the red-shifted chlorophylls c1/c2 due to the protonation of the acrylate group. We present a model that describes an open and a closed form of the protonated/deprotonated chlorophylls c1/c2-acrylate-H2O moiety that controls the proton loading site in the photoprotective and light harvesting state.

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Andreou, C., & Varotsis, C. (2025). Light harvesting and photoprotective states in the marine diatom Fragilariopsis sp.: functional implications of chlorophylls c1/c2 in the fucoxanthin-chlorophyll a/c-binding proteins (FCPs). RSC Advances, 15(6), 4322–4330. https://doi.org/10.1039/d4ra06711h

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