The photochemistry of C-phycocyanin has been studied after denaturation in the dark. It shows
an irreversible reaction which has characteristics of a Ζ,Ζ,Ε- to Z,Z,Z-isomerization of dihydrobilins.
Its amplitude depends on the reaction conditions, with a maximum corresponding to 15%
conversion of one of the three PC chromophores. This chromophore is suggested to be ß-153, for
which recent X-ray data T. Schirmer, W. Bode, and R. Huber, J. Mol. Biol., submitted, show
ring D being highly twisted out of the plane of the other rings. During unfolding, there is thus a
probability of falling into the photochemically labile Z,Z,^-configuration
