C. Johannes et al., DEGRADATION OF ANTHRACENE BY LACCASE OF TRAMETES-VERSICOLOR IN THE PRESENCE OF DIFFERENT MEDIATOR COMPOUNDS, Applied microbiology and biotechnology, 46(3), 1996, pp. 313-317
Laccase of Trametes versicolor was generally able to oxidize anthracen
e in vitro. After 72 h incubation about 35% of the anthracene was tran
sformed stoichiometrically to 9,10-anthraquinone. Transformation of an
thracene increased rapidly in the presence of different mediators that
readily generate stable radicals: 2,2'-azino-bis-(3-ethylbenzthiazoli
ne-6-sulfonic acid) (ABTS) and 1-hydroxybenzotriazole. For the reactio
n, the presence of both the laccase and the mediator was necessary. In
the presence of 0.005 mM 1-hydroxybenzotriazole this conversion had r
emoved 47% of the anthracene after 72 h; 75% of the substrate was oxid
ized during this period when ABTS (1 mM) was used as mediator. In cont
rast to reactions without or with only low concentrations of a mediato
r, there was a discrepancy between the disappearance of anthracene and
the formation of 9,10-anthraquinone in mediator-forced reactions. Cou
pling-products of mediators with anthracene degradation products were
found. Anthracene disappeared nearly completely after incubation for 7
2 h with laccase in a 0.1 mM solution of 1-hydroxybenzotriazole and wa
s transformed to 9,10-anthraquinone in about 80% yield; 90% of the sub
strate was transformed in the presence of ABTS (2.0 mM) resulting agai
n in 80% quinone. Phenothiazine was not effective in this system.