Abstract
The absorption and fluorescence behaviour of the circadian blue-light photoreceptor cryptochrome from Drosophila melanogaster (dCry) in a pH 8 aqueous buffer solution is studied. The flavin adenine dinucleotide (FAD) cofactor of dCry is identified to be present in its oxidized form (FAD(ox)), and the 5,10-methenyltetrahydrofolate (MTHF) cofactor is found to be hydrolyzed and oxidized to ...
Abstract
The absorption and fluorescence behaviour of the circadian blue-light photoreceptor cryptochrome from Drosophila melanogaster (dCry) in a pH 8 aqueous buffer solution is studied. The flavin adenine dinucleotide (FAD) cofactor of dCry is identified to be present in its oxidized form (FAD(ox)), and the 5,10-methenyltetrahydrofolate (MTHF) cofactor is found to be hydrolyzed and oxidized to 10-formyldihydrofolate (10-FDHF). The absorption and the fluorescence behaviour of dCry is investigated in the dark-adapted (receptor) state, the light-adapted (signalling) state, and under long-time violet light exposure. Photoexcitation of FAD(ox) in dCry causes a reductive electron transfer to the formation of anionic FAD semiquinone (FAD(center dot-)), and photo-excitation of the generated FAD(center dot-) causes an oxidative electron transfer to the back formation of FAD(ox). In light adapted dCry a photo-induced equilibrium between FAD(ox) and FAD(center dot-)exists. The photo-cycle dynamics of signalling state formation and recovery is discussed. Quantum yields of photo-induced signalling state formation of about 0.2 and of photo-induced back-conversion of about 0.2 are determined. A recovery of FAD(center dot-) to FAD(ox) in the dark with a time constant of 1.6 min at room temperature is found. (C) 2008 Elsevier B.V. All rights reserved.
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