The photochemical mechanism of a B 12-dependent photoreceptor protein

© 2015 Macmillan Publishers Limited. All rights reserved. The coenzyme B 12 -dependent photoreceptor protein, CarH, is a bacterial transcriptional regulator that controls the biosynthesis of carotenoids in response to light. On binding of coenzyme B 12 the monomeric apoprotein forms tetramers in the dark, which bind operator DNA thus blocking transcription. Under illumination the CarH tetramer dissociates, weakening its affinity for DNA and allowing transcription. The mechanism by which this occurs is unknown. Here we describe the photochemistry in CarH that ultimately triggers tetramer dissociation; it proceeds via a cob(III)alamin intermediate, which then forms a stable adduct with the protein. This pathway is without precedent and our data suggest it is independent of the radical chemistry common to both coenzyme B 12 enzymology and its known photochemistry. It provides a mechanistic foundation for the emerging field of B 12 photobiology and will serve to inform the development of a new class of optogenetic tool for the control of gene expression.Peer Reviewe

The photochemical mechanism of a B12-dependent photoreceptor protein

The coenzyme B(12)-dependent photoreceptor protein, CarH, is a bacterial transcriptional regulator that controls the biosynthesis of carotenoids in response to light. On binding of coenzyme B(12) the monomeric apoprotein forms tetramers in the dark, which bind operator DNA thus blocking transcription. Under illumination the CarH tetramer dissociates, weakening its affinity for DNA and allowing transcription. The mechanism by which this occurs is unknown. Here we describe the photochemistry in CarH that ultimately triggers tetramer dissociation; it proceeds via a cob(III)alamin intermediate, which then forms a stable adduct with the protein. This pathway is without precedent and our data suggest it is independent of the radical chemistry common to both coenzyme B(12) enzymology and its known photochemistry. It provides a mechanistic foundation for the emerging field of B(12) photobiology and will serve to inform the development of a new class of optogenetic tool for the control of gene expression