Pj. Collins et al., OXIDATION OF ANTHRACENE AND BENZO[A]PYRENE BY LACCASES FROM TRAMETES-VERSICOLOR, Applied and environmental microbiology, 62(12), 1996, pp. 4563-4567
The in vitro oxidation of the two polycyclic aromatic hydrocarbons ant
hracene and benzo[a]pyrene, which have ionization potentials of less t
han or equal to 7.45 eV, is catalyzed by laccases from Trametes versic
olor. Crude laccase preparations were able to oxidize both anthracene
and the potent carcinogen benzo[a]pyrene. Oxidation of benzo [a] pyren
e was enhanced by the addition of the cooxidant 2,2'-azinobis(3-ethylb
enzthiazoline-6-sulfonate) (ABTS), while an increased anthracene oxidi
zing ability was observed in the presence of the low-molecular-weight
culture fluid ultrafiltrate. Two purified laccase isozymes from T. ver
sicolor were found to have similar oxidative activities towards anthra
cene and benzo[a]pyrene. Oxidation of anthracene by the purified isozy
mes was enhanced in the presence of ABTS, while ABTS was essential for
the oxidation of benzo[a]pyrene. In all cases anthraquinone was ident
ified as the major end product of anthracene oxidation, These findings
indicate that laccases may have a role in the oxidation of polycyclic
aromatic hydrocarbons by white rot fungi.