Author:
Balakshin Mikhail Yu.,Chen Chen-Loung,Gratzl Josef S.,Kirkman Adrianna G.,Jakob Harald
Abstract
Summary
The kinetics of dioxygen uptake in the laccase-catalyzed oxidation of veratryl alcohol with dioxygen in
the presence of ABTS, the mediator, was studied. The kinetics of dioxygen uptake consists of two phases:
(1) the initial phase up to a reaction time of one hour, and (2) the second phase, after a reaction time
of one hour. In the initial phase, ABTS is mainly oxidized to the corresponding cation radical. The kinetics
of dioxygen uptake follows a pseudo-zero order rate law. The dioxygen uptake under the reaction
condition correlates with the initial ABTS concentration according to the stoichiometric relationship of
0.25 moles dioxygen per mole ABTS. In the second phase, veratryl alcohol is mainly oxidized to veratraldehyde.
The kinetics of the dioxygen uptake follows a pseudo-first order rate law. The dioxygen
uptake correlates linearly with the yield of veratraldehyde. The stoichiometric ratio between the formation
of veratraldehyde and the consumption of dioxygen differs slightly at different M/S ratios. On average,
however, it is 0.42 moles of dioxygen per one mole of veratraldehyde formed. The reaction mechanism
is discussed on the basis of the kinetic data.
Cited by
19 articles.
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