ArticleBioMed research international2013
Degradation of diuron by Phanerochaete chrysosporium: role of ligninolytic enzymes and cytochrome P450.
Article in BioMed research international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 58 citations in OpenAlex.
- Toxic Effects of p-Chloroaniline on Cells of FungusToxics · 2025Article
- Performance evaluation of Trichoderma reseei in tolerance and biodegradation of diuron herbicide in agar plate, liquid culture and solid-state fermentation.World journal of microbiology & biotechnology · 2024Article
- Micropollutant removal capacity and stability of aquaporin incorporated biomimetic thin-film composite membranes.Biotechnology reports (Amsterdam, Netherlands) · 2022Article
- Degradation of 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) by fungi originating from Vietnam.Biodegradation · 2022Article
- Emerging Strategies for the Bioremediation of the Phenylurea Herbicide Diuron.Frontiers in microbiology · 2021Review
- Degradation of the Organochlorinated Herbicide Diuron by Rainforest Basidiomycetes.BioMed research international · 2020Article
- Gene Expression Analysis of Three Putative Copper-Transporting ATPases in Copper-TolerantFrontiers in microbiology · 2020Article
- Ligninolytic behavior of the white-rot fungus3 Biotech · 2019Article
- 1-Aminobenzotriazole: A Mechanism-Based Cytochrome P450 Inhibitor and Probe of Cytochrome P450 Biology.Medicinal chemistry · 2018Article
- Article
- Modeling Based Structural Insights into Biodegradation of the Herbicide Diuron by Laccase-1 from Ceriporiopsis subvermispora.Bioinformation · 2015Article
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The white-rot fungus Phanerochaete chrysosporium was investigated for its capacity to degrade the herbicide diuron in liquid stationary cultures. The presence of diuron increased the production of lignin peroxidase in relation to control cultures but only barely affected the production of manganese peroxidase. The herbicide at the concentration of 7 μ g/mL did not cause any reduction in the biomass production and it was almost completely removed after 10 days. Concomitantly with the removal of diuron, two metabolites, DCPMU [1-(3,4-dichlorophenyl)-3-methylurea] and DCPU [(3,4-dichlorophenyl)urea], were detected in the culture medium at the concentrations of 0.74 μ g/mL and 0.06 μ g/mL, respectively. Crude extracellular ligninolytic enzymes were not efficient in the in vitro degradation of diuron. In addition, 1-aminobenzotriazole (ABT), a cytochrome P450 inhibitor, significantly inhibited both diuron degradation and metabolites production. Significant reduction in the toxicity evaluated by the Lactuca sativa L. bioassay was observed in the cultures after 10 days of cultivation. In conclusion, P. chrysosporium can efficiently metabolize diuron without the accumulation of toxic products.
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