Carotenoid pigment co-oxidation by lipoxygenase has been studied by
factorially combining three
pigments: β-carotene, capsanthin, and diesterified capsanthin; two
environmental conditions:
presence or absence of light; three oxidant conditions in the same
reaction medium: presence of
both lipoxygenase and linoleic acid, presence of linoleic acid only,
and absence of both; and four
temperatures: 15, 25, 35, and 45 °C. Independently of the
presence or absence of enzyme, diesterified
capsanthin and β-carotene were the most unstable pigments, and both
exhibited similar lability,
although nonesterified capsanthin showed a great stability. This
different behavior among pigments
could be related with their polarity. The overall reaction clearly
follows a first-order kinetic model
and the thermodynamic parameters reveal that the co-oxidation reactions
of carotenoids are multiple
isokinetic forms of just one reaction. In all of the cases
studied, enzymatic or nonenzymatic decoloring
of carotenoids is a theoretical reaction that can be explained as a
loss of conjugation in a sequence
of conjugated double bonds. The source of pro-oxidant compounds,
the environmental conditions,
the reaction medium, and the differences in pigment structure are
external factors that modify the
kinetic parameters of the reaction and consequently the thermodynamic
parameters, but not the
reaction pathway.
Keywords: Carotenoids; lipoxygenase; decoloring; degradation;
kinetic