Abstract
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.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Biologie |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 570 Biowissenschaften; Biologie |
URN: | urn:nbn:de:bvb:19-epub-2224-5 |
ISSN: | 0341-0382, 0341-0471, 0939-5075 |
Signatur: | 2 Bcher BSB:4 Z 46.13-42,c,1/5 und BSB:4 Z 46.13-42,c,6/12 |
Sprache: | Englisch |
Dokumenten ID: | 2224 |
Datum der Veröffentlichung auf Open Access LMU: | 12. Mrz. 2008, 13:03 |
Letzte Änderungen: | 04. Nov. 2020, 12:46 |