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Dibutyl phthalate (DBP) is a widely used plasticizer, whose presence in the environment as a pollutant raises concern because of its endocrine-disrupting toxicity. Growth kinetics, glucose uptake, biodegradation constant of DBP ( k), half-life of DBP biodegradation ( t) and percentage of removal efficiency (% E) were evaluated for Fusarium culmorum grown on media containing glucose and different concentrations of DBP (500 and 1000 mg/l). Intermediate compounds of biodegraded DBP were identified by GC-MS and a novel DBP biodegradation pathway was proposed on the basis of the intermolecular flow of electrons of the intermediates identified using quantum chemical modeling. F. culmorum degraded 99% of both 1000 and 500 mg of DBP/l after an incubation period of 168 and 228 h, respectively. % E was 99.5 and 99.3 for 1000 and 500 mg of DBP/l, respectively. The k was 0.0164 and 0.0231 h for 500 and 1000 mg of DBP/l, respectively. DBP was fully metabolized to fumaric and malic acids, which are compounds that enter into the Krebs cycle. F. culmorum has a promising ability for bioremediation of environments polluted with DBP because it efficiently degrades DBP and uses high concentrations of this compound as carbon and energy source. [ABSTRACT FROM AUTHOR]

Di(2-ethylhexyl) phthalate (DEHP) is a plasticizer that is widely used to soften plastic products. It is an endocrine-disrupting compound, widely considered an environmental contaminant that is difficult to remove or degrade. The radial growth rate (ur), mycelial biomass, intracellular and extracellular activities of laccase and esterase, intracellular and extracellular contents of protein and glycogen, and the contents of soluble and insoluble glucans were evaluated in colonies of Lentinula edodes, grown in various concentrations of DEHP (0, 750, 1200, and 1500 mg/L) on agar. Glucose and yeast extracts were added to all media. The highest ur was shown in medium lacking DEHP, followed by that shown in the medium containing 1500 mg of DEHP/L. The greatest protein extracellular contents were observed in medium with added DEHP. The largest extracellular glycogen contents and mycelial biomass were found in media containing 1200 and 1500 mg of DEHP/L, respectively. These results suggest that DEHP was degraded and used as a substrate by L. edodes during diauxic growth (glucose metabolized first, followed by DEHP), and laccases were more important than esterases in the metabolism of DEHP. L. edodes can be used to remove DEHP from phthalate-polluted environments. [ABSTRACT FROM AUTHOR]