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Chemical compound From Wikipedia, the free encyclopedia
Myxoxanthophyll is a carotenoid glycoside pigment present (usually as rhamnosides) in the photosynthetic apparatus of cyanobacteria.[1] It is named after the word "Myxophyceae", a former term for cyanobacteria.[2] As a monocyclic xanthophyll, it has a yellowish color. It is required for normal cell wall structure and thylakoid organization in the cyanobacterium Synechocystis.[3] The pigment is unusual because it is glycosylated on the 2'-OH rather than the 1'-OH position of the molecule.[2] Myxoxanthophyll was first isolated from Oscillatoria rubenscens in 1936.[4]
Names | |
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IUPAC name
(3S,4R,5S)-2-[(4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2-hydroxy-25-(4-hydroxy-2,6,6-trimethylcyclohexen-1-yl)-2,6,10,14,19,23-hexamethylpentacosa-4,6,8,10,12,14,16,18,20,22,24-undecaen-3-yl]oxy-6-methyloxane-3,4,5-triol | |
Other names
Myxoxanthophyll, myxol-2' fucoside | |
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3D model (JSmol) |
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Properties | |
C46H66O7 | |
Molar mass | 731.012 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The bright red pigment lycopene is the acyclic precursor of all carotenoids in cyanobacteria. In myxoxanthophyll synthesis, lycopene is enzymatically converted to 1-hydroxylycoprene, then to intermediates 1'-hydroxy-y-carotene, plectaniaxanthin, and myxol. Finally, the hydroxyl group in myxol is glycosylated at the 2' position to form myxoxanthophyll.[2]
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