Degradation of organophosphate flame retardants by white-rot fungi
The environmental persistence of organophosphate flame retardants (OPFRs) in water is becoming and environmental concern. White Rot Fungi (WRF) have proven its capability to degrade certain OPFRs such as tributyl phosphate (TBP), tris(2-butoxyethyl) phosphate (TBEP), tris(2-chloroethyl) phosphate (T...
| Autores: | , , , , , |
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| Tipo de documento: | artigo |
| Data de publicação: | 2025 |
| País: | España |
| Recursos: | Universitat Autònoma de Barcelona |
| Repositório: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglês |
| OAI Identifier: | oai:ddd.uab.cat:309982 |
| Acesso em linha: | https://ddd.uab.cat/record/309982 https://dx.doi.org/urn:doi:10.1016/j.scitotenv.2024.178260 |
| Access Level: | Acceso aberto |
| Palavra-chave: | Biodegradation Demethylation Hydroxylation OPFRs Transformation products Biodegradation, Environmental Organophosphates/metabolism Water Pollutants, Chemical/metabolism Animals Flame Retardants/metabolism Basidiomycota/metabolism Organophosphorus Compounds/metabolism |
| Resumo: | The environmental persistence of organophosphate flame retardants (OPFRs) in water is becoming and environmental concern. White Rot Fungi (WRF) have proven its capability to degrade certain OPFRs such as tributyl phosphate (TBP), tris(2-butoxyethyl) phosphate (TBEP), tris(2-chloroethyl) phosphate (TCEP) and tris(2-chloroisopropyl) phosphate (TCPP). Despite this capability, there is limited knowledge about the specific pathways involved in the degradation. In this study, three different WRF were paired with individual OPFRs, and potential transformation products (TPs) were identified by UHPLC-HRMS. Some compounds structures were further validated by NMR. From these data degradation pathways were proposed. TBP was degraded by successive hydroxylation and hydrolysis reactions, with a novel dehydrogenation step suggested. Both TCEP and TCPP underwent oxidative dechlorination, with TCEP experiencing subsequent hydrolysis. Uncommon reductive dehalogenation was also observed. TCPP further underwent hydroxylation and environmentally relevant methylation. TBEP generated numerous TPs, mainly by successive dealkylations, along with hydroxylation. Notably, demethylation in TBEP degradation was proposed for the first time. Additional secondary products were formed through hydroxylation and oxidation of the initial metabolites. Finally, in vivo and in silico toxicity assessments were conducted, identifying certain TPs as potentially toxic. |
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