4.4 Article

Primary Photochemistry of the Dark- and Light-Adapted States of the YtvA Protein from Bacillus subtilis

Journal

BIOCHEMISTRY
Volume 52, Issue 45, Pages 7951-7963

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bi4012258

Keywords

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Funding

  1. Human Frontiers Science Organization [CDA0016/2007-C]

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The primary (100 fs to 10 ns) and secondary (10 ns to 100 mu s) photodynamics in the type II-light-oxygen-voltage (LOV) domain from the blue light YtvA photoreceptor extracted from Bacillus subtilis were explored with transient absorption spectroscopy. The photodynamics of full-length YtvA were characterized after femtosecond 400 nm excitation of both the dark-adapted D-447 state and the light-adapted S-390 state. The S-390 state relaxes on a 43 min time scale at room temperature back into D-447, which is weakly accelerated by the introduction of imidazole. This is ascribed to an obstructed cavity in YtvA that hinders access to the embedded FMN chromophore and is more open in type I LOV domains. The primary photochemistry of dark-adapted YtvA is qualitatively similar to that of the type I LOV domains, including AsLOV2 from Avena sativa, but exhibits an appreciably higher (60% greater) terminal triplet yield, estimated near the maximal Phi(ISC) value of approximate to 78%; the other 22% decays via non-triplet-generating fluorescence. The subsequent secondary dynamics are inhomogeneous, with three triplet populations co-evolving: the faster-decaying T-I* population (38% occupancy) with a 200 ns decay time is nonproductive in generating the S-390 adduct state, a slower T-II* population (57% occupancy) exhibits a high yield (Phi(adduct) approximate to 100%) in generating S-390 and a third (5%) T-III* population persists (>100 mu s) with unresolved photoactivity. The ultrafast photoswitching dynamics of the S-390 state appreciably differ from those previously resolved for the type I AcLOV2 domain from Adiantum capillus-veneris [Kennis, J. T., et al. (2004) J. Am. Chem. Soc. 126, 4512], with a low-yield dissociation (Phi(dis) approximate to 2.5%) reaction, which is due to an ultrafast recombination reaction, following photodissociation, and is absent in AcLOV2, which results in the increased photoswitching activity of the latter domain.

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