Chlorhexidine (CHX) and octenidine (OCT), antimicrobial compounds used in oral care products (toothpastes and mouthwashes), were recently revealed to interfere with human sex hormone receptor pathways. Experiments employing model organisms-white-rot fungi Irpex lacteus and Pleurotus ostreatus-were carried out in order to investigate the biodegradability of these endocrine-disrupting compounds and the capability of the fungi and their extracellular enzyme apparatuses to biodegrade CHX and OCT. Up to 70% ± 6% of CHX was eliminated in comparison with a heat-killed control after 21 days of in vivo incubation. An additional in vitro experiment confirmed manganese-dependent peroxidase and laccase are partially responsible for the removal of CHX. Up to 48% ± 7% of OCT was removed in the same in vivo experiment, but the strong sorption of OCT on fungal biomass prevented a clear evaluation of the involvement of the fungi or extracellular enzymes. On the other hand, metabolites indicating the enzymatic transformation of both CHX and OCT were detected and their chemical structures were proposed by means of liquid chromatography-mass spectrometry. Complete biodegradation by the ligninolytic fungi was not achieved for any of the studied analytes, which emphasizes their recalcitrant character with low possibility to be removed from the environment.

• Keywords
• chlorhexidine, dental hygiene, laccase, ligninolytic fungi, manganese-dependent peroxidase, octenidine, personal care products, quaternary ammonium compounds, recalcitrant pollutant,
• MeSH
• Anti-Infective Agents, Local metabolism   MeSH
• Biodegradation, Environmental * MeSH
• Chlorhexidine chemistry   metabolism   MeSH
• Fungi metabolism   MeSH
• Imines MeSH
• Humans MeSH
• Metabolomics methods   MeSH
• Pyridines chemistry   metabolism   MeSH
• Dental Care MeSH
• Transformation, Genetic MeSH
• Check Tag
• Humans MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• Anti-Infective Agents, Local MeSH
• Chlorhexidine MeSH
• Imines MeSH
• octenidine MeSH Browser
• Pyridines MeSH

White-rot fungi that are efficient lignin degraders responsible for its turnover in nature have appeared twice in the center of biotechnological research - first, when the lignin degradation process started being systematically investigated and major enzyme activities and mechanisms involved were described, and second, when the huge remediation potential of these organisms was established. Originally, Phanerochaete chrysosporium became a model organism, characterized by a secondary metabolism regulatory pattern triggered by nutrient (mostly nitrogen) limitation. Last decade brought evidence of more varied regulatory patterns in white-rot fungi when ligninolytic enzymes were also abundantly synthesized under conditions of nitrogen sufficiency. Gradually, research was focused on other species, among them Irpex lacteus showing a remarkable pollutant toxicity resistance and biodegradation efficiency. Systematic research has built up knowledge of biochemistry and biotechnological applicability of this fungus, stressing the need to critically summarize and estimate these scattered data. The review attempts to evaluate the information on I. lacteus focusing on various enzyme activities and bioremediation of organopollutants in water and soil environments, with the aim of mediating this knowledge to a broader microbiological audience.

• MeSH
• Basidiomycota enzymology   genetics   metabolism   MeSH
• Biodegradation, Environmental MeSH
• Biotechnology * MeSH
• Fungal Proteins genetics   metabolism   MeSH
• Environmental Pollutants metabolism   MeSH
• Lignin metabolism   MeSH
• Gene Expression Regulation, Fungal MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Review MeSH
• Names of Substances
• Fungal Proteins MeSH
• Environmental Pollutants MeSH
• Lignin MeSH

The ligninolytic fungus Irpex lacteus was shown as an efficient degrader of oligocyclic aromatic hydrocarbons (PAHs; 'polycyclic aromatic hydrocarbons') possessing 3-6 aromatic rings in complex liquid media. The strain produced mainly Mn-dependent peroxidase in media without pollutants. Activity of ligninolytic enzymes was higher in a N-limited medium. However, after contamination with PAHs (especially pyrene) the values increased and significant activity of Mn-independent peroxidase appeared in the complex medium. Other factors (such as the increase in nitrogen concentration or the presence of solvent(s) for dissolution of PAHs) had no effect. Cytochrome P-450 was detected in the microsomal fraction of biomass grown in the complex medium. The rate of PAH degradation was also affected by the presence of various combinations of PAHs. However, independently of the enzyme activities, anthracene was shown to have a positive influence on degradation of pyrene and fluoranthene.

• MeSH
• Basidiomycota enzymology   genetics   metabolism   MeSH
• Biodegradation, Environmental MeSH
• Fungal Proteins genetics   metabolism   MeSH
• Lignin metabolism   MeSH
• Peroxidases genetics   metabolism   MeSH
• Polycyclic Aromatic Hydrocarbons chemistry   metabolism   MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Fungal Proteins MeSH
• Lignin MeSH
• Peroxidases MeSH
• Polycyclic Aromatic Hydrocarbons MeSH

The effect of enhanced laccase (Lac) activity (obtained after copper addition to cultivation media) on decolorization of azo dye Orange G in two basidiospore-derived monokaryotic isolates of Pleurotus ostreatus was determined. The high Lac-producing isolate efficiently decolorized Orange G. The low-producing isolate showed only poor decolorization ability during cultivation in liquid medium and no decolorization on agar plates containing Orange G after a 25-d growth. A substantial enhancement of Lac activity caused by copper addition into cultivation media was detected in both isolates but, at the same time, the biomass production decreased and decolorization rate was reduced.

• MeSH
• Enzyme Activation drug effects   MeSH
• Azo Compounds metabolism   MeSH
• Laccase metabolism   MeSH
• Environmental Pollutants metabolism   MeSH
• Copper pharmacology   MeSH
• Peroxidases metabolism   MeSH
• Pleurotus classification   enzymology   MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Azo Compounds MeSH
• Laccase MeSH
• Environmental Pollutants MeSH
• manganese peroxidase MeSH Browser
• Copper MeSH
• Orange G MeSH Browser
• Peroxidases MeSH

The ability to decolorize four synthetic dyes (Phenol Red, Evans Blue, Eosin Yellowish and Poly B411) in five Pleurotus ostreatus strains (a parental strain and four isolates derived from it) was determined. Two of the isolates had markedly higher and other two substantially lower production of ligninolytic enzymes and hydrogen peroxide than the parental strain. Like the parental strain, the higher-producing isolates were able to decolorize all the tested dyes, but not to a higher extent than the parental strain. In contrast, two lower-producing isolates exhibited slow decolorization, which was incomplete even at the end of cultivation. Evans Blue and Eosin Yellowish strongly suppressed the growth of the strains, while Phenol Red and Poly B411 induced none or only a very slight growth reduction.

• MeSH
• Color MeSH
• Coloring Agents metabolism   MeSH
• Laccase MeSH
• Oxidoreductases metabolism   MeSH
• Hydrogen Peroxide metabolism   MeSH
• Peroxidases metabolism   MeSH
• Pleurotus chemistry   enzymology   metabolism   MeSH
• Textile Industry MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Coloring Agents MeSH
• Laccase MeSH
• manganese peroxidase MeSH Browser
• Oxidoreductases MeSH
• Hydrogen Peroxide MeSH
• Peroxidases MeSH