Journal
PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
Volume 14, Issue 2, Pages 288-299Publisher
SPRINGERNATURE
DOI: 10.1039/c4pp00155a
Keywords
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Funding
- German Science Foundation (Deutsche Forschungsgemeinschaft, DFG) [GRK-1626]
- DFG [Di299/6]
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LOV domains are the light sensitive parts of phototropins and many other light-activated enzymes that regulate the response to blue light in plants and algae as well as some fungi and bacteria. Unlike all other biological photoreceptors known so far, the photocycle of LOV domains involves the excited triplet state of the chromophore. This chromophore is flavin mononucleotide (FMN) which forms a covalent adduct with a cysteine residue in the signaling state. Since the formation of this adduct from the triplet state involves breaking and forming of two bonds as well as a change from the triplet to the singlet spin state, various intermediates have been proposed, e. g. a protonated triplet state (FMNH+)-F-3, the radical anion (FMN center dot-)-F-2, or the neutral semiquinone radical (FMNH center dot)-F-2. We performed an extensive search for these intermediates by two-dimensional transient absorption (2D-TA) with a streak camera. However, no transient with a rate constant between the decay of fluorescence and the decay of the triplet state could be detected. Analysis of the decay associated difference spectra results in quantum yields for the formation of the adduct from the triplet of Phi(A)(LOV1) approximate to 0.75 and Phi(A)(LOV2) approximate to 0.80. This is lower than the values Phi(A)(LOV1) approximate to 0.95 and Phi(A)(LOV2) approximate to 0.99 calculated from the rate constants, giving indirect evidence of an intermediate that reacts either to form the adduct or to decay back to the ground state. Since there is no measurable delay between the decay of the triplet and the formation of the adduct, we conclude that this intermediate reacts much faster than it is formed. The LOV1-C57S mutant shows a weak and slowly decaying (tau > 100 mu s) transient whose decay associated spectrum has bands at 375 and 500 nm, with a shoulder at 400 nm. This transient is insensitive to the pH change in the range 6.5-10.0 but increases on addition of beta-mercaptoethanol as the reducing agent. We assign this intermediate to the radical anion which is protected from protonation by the protein. We propose that the adduct is formed via the same intermediate by combination of the radical ion pair.
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