Phycocyanobilin
From Wikipedia, the free encyclopedia
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| Names | |
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| IUPAC name
(2R,3E)-18-ethyl-3-ethylidene-1,2,3,19,22,24-hexahydro-2,7,13,17-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropanoic acid | |
| Identifiers | |
3D model (JSmol) |
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| 4285356 | |
| ChEBI | |
| ChemSpider | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C33H38N4O6 | |
| Molar mass | 586.69 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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Phycocyanobilin is a blue phycobilin, i.e., a tetrapyrrole chromophore found in cyanobacteria and in the chloroplasts of red algae, glaucophytes, and some cryptomonads. Phycocyanobilin is present only in the phycobiliproteins allophycocyanin and phycocyanin, of which it is the terminal acceptor of energy. It is covalently linked to these phycobiliproteins by a thioether bond.
Phycocyanobilin (PCB), has the ability to bind to human serum albumin (HSA), protein found mainly in the blood of humans. This PCB-HCA complex benefits the structure of HSA, increasing the thermal stability of HSA, as well as increasing its ability to prevent against proteolytic activity of other proteins.[1]
The biosynthetic pathway of phycocyanobilin begins with 5-aminolevulinic acid (5-ALA).[2] Two molecules of 5-ALA undergo a condensation reaction catalyzed by porphobilinogen synthase to yield a molecule of porphobilinogen (PBG) (not shown).[3] Four molecules of PBG are polymerized into a linear tetrapyrrole by porphobilinogen deaminase. This reaction releases four ammonia molecules in the process. Completion of the tetrapyrrole is performed by uroporphyrinogen III synthase which results in the macrocyclic Uroporphyrinogen III. Uroporphyrinogen III is then converted to a heme by uroporphyrinogen III decarboxylase. The heme molecule is converted to biliverdin. This is reduced to phycocyanobilin by phycocyanobilin:ferredoxin oxidoreductase PcyA.[4][2]