Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Lycopene enzymatic cleavage

The second pathway is the eccentric cleavage that occurs at double bonds other than the central 15,15 -double bond of the P-carotene molecule to produce different products called P-apocarotenals with various chain lengths. Because only trace amounts of apocarotenals were detected in vivo from tissues of animals fed P-carotene and these compounds can be formed non-enzymatically from P-carotene auto-oxidation, the existence of this pathway was controversial until recently. The identification of P-carotene 9, 10 -oxygenase (BC02), which acts specifically at the 9, 10 double bond of P-carotene to produce P-apo-lO -carotenal and P-ionone, provided clear evidence of the eccentric cleavage pathway in vivo. Lycopene was also reported as a substrate for BC02 activity. [Pg.164]


See other pages where Lycopene enzymatic cleavage is mentioned: [Pg.417]    [Pg.419]    [Pg.421]    [Pg.424]    [Pg.323]    [Pg.324]    [Pg.3886]    [Pg.322]    [Pg.327]   


SEARCH



Enzymatic cleavage

Lycopenal

Lycopene

© 2024 chempedia.info