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Schmidt, G.; Siebzehnrübl, S.; Fischer, R.; Rüdiger, W.; Scheer, Hugo; Schirmer, T.; Bode, W.; Huber, R. (1987): ZZE-Configuration of chromophore ß-153 in C-phycocyanin from Mastigocladus laminosus. In: Zeitschrift für Naturforschung C, Vol. 42c: pp. 845-848




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.