K. Lisowska et J. Dlugonski, Removal of anthracene and phenanthrene by filamentous fungi capable of cortexolone 11-hydroxylation, J BASIC MIC, 39(2), 1999, pp. 117-125
Nine fungal strains showing ability of cortexolone hydroxylation to epicort
isol and/or cortisol were screened in this work for anthracene and phenanth
rene elimination (250 mg/l). All of the strains (Cylindrocladium simplex IM
2358, C. simplex IM 2358/650, Monosporium olivaceum IM 484, Curvularia lun
ata IM 2901, C. lunata IM 2901/366, C. tuberculata IM 4417, Cunninghamella
elegans IM 1785, C. elegans IM 1785/21Gp, C. elegans IM 1785/10Gi) signific
antly removed anthracene and phenanthrene. During incubation with anthracen
e formation of intermediate products was observed. The amount of the main i
ntermediate product, identified as 9,10-anthraquinone, was not greater than
22.2% of the anthracene introduced to the fungal cultures. C. elegans IM 1
785/21Gp was the best degrader of both anthrarene and phenanthrene, removin
g 81.6 and 99.4% of these compounds after 7 days, respectively. Phenanthren
e removal by C. elegans IM 1785/21Gp was preceded by PAHs accumulation in m
ycelium and growth inhibition. Elimination of phenanthrene started after on
e day of incubation and was related to the fungus growth.