Plant and Cell Physiology, 2001, Vol. 42, No. 7 756-762
© 2001 Oxford University Press
Myxoxanthophyll in Synechocystis sp. PCC 6803 is Myxol 2'-Dimethyl-Fucoside, (3R,2'S)-Myxol 2'-(2,4-di-O-Methyl-
-L-Fucoside), not Rhamnoside
1 Biological Laboratory, Nippon Medical School, Kawasaki, 211-0063 Japan 2 Kyoto Pharmaceutical University, Kyoto, 607-8414 Japan 3 Biological Laboratory, Faculty of Education, Kumamoto University, Kumamoto, 860-8555 Japan
We identified the molecular structures of the carotenoids in Synechocystis sp. PCC 6803. Myxoxanthophyll in this cyanobacterium was myxol 2'-dimethyl-fucoside, (3R,2'S)-myxol 2'-(2,4-di-O-methyl-
-L-fucoside). The sugar moiety of the pigment was not rhamnose but dimethylated fucose, which has not been reported in carotenoid glycosides. The other carotenoids were ß-carotene, (3R,3'R)-zeaxanthin, echinenone, (3'R)-3'-hydroxyechinenone and deoxymyxol 2'-dimethyl-fucoside, (2'S)-deoxymyxol 2'-(2,4-di-O-methyl-
-L-fucoside). Generally, the group of polar carotenoids in cyanobacteria is referred to as myxoxanthophyll, and the structure is considered to be myxol 2'-rhamnoside. Since the name myxoxanthophyll can not specify the sugar moiety and the identification of the sugar moiety is unfeasible in many cyanobacteria, we propose the following naming convention: when the sugar moiety is unknown, the name is myxol glycoside, when known, as in the case of rhamnose and
-L-fucose, they should be named myxol 2'-rhamnoside and myxol 2'-
-L-fucoside, respectively.
4 Corresponding author: E-mail, takaichi/biology@nms.ac.jp; Fax, +81-44-722-1231.
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