Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-7939
Main Title: Isolation of the Phytochrome Chromophore. The Cleavage Reaction with Hydrogen Bromide
Author(s): Rüdiger, Wolfhart
Brandlmeier, Thomas
Blos, Inge
Gossauer, Albert
Weller, Jens-Peter
Type: Article
Language Code: en
Abstract: The cleavage of the bilin chromophore from C-phycocyanin with hydrogen bromide yields 3E-configurated phycocyanobilin (4) as the major and 3 Z-configurated phycocyanobilin (5) as the minor reaction product. The reaction of synthetic 3E-configurated phytochromobilin (2) with hydrogen bromide and methanol leads only to a methanol adduct at the C-18 side chain (7) whereas the same reaction with the 3Z-configurated phytochromobilin (3) leads to 7 and 2. The bilin chromophore was cleaved also from phytochrome after preparation of phytochromobilin peptides. The detection of 2 and 7 suggested that 3Z-and 3E-configurated phytochromobilin were the primary products of cleavage from phytochrome. A reaction scheme is given which can explain the results of the reaction with hydrogen bromide and methanol.
URI: https://depositonce.tu-berlin.de//handle/11303/8810
http://dx.doi.org/10.14279/depositonce-7939
Issue Date: 1980
Date Available: 4-Jan-2019
DDC Class: 570 Biowissenschaften; Biologie
Subject(s): phytochrome
bile pigments
phytochromobilin
thioether cleavage
c-phycocyanin
License: https://creativecommons.org/licenses/by-nc-nd/3.0/
Journal Title: Zeitschrift für Naturforschung C
Publisher: De Gruyter
Publisher Place: Berlin
Volume: 35
Issue: 9-10
Publisher DOI: 10.1515/znc-1980-9-1018
Page Start: 763
Page End: 769
EISSN: 1865-7125
ISSN: 0939-5075
Appears in Collections:FG Organische Chemie » Publications

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