Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Av. da República, 2780-157 Oeiras, Portugal.
Department of Analytical Chemistry, University of Barcelona, Diagonal 645, E-08028 Barcelona, Spain.
J Hazard Mater. 2014 Mar 15;268:264-72. doi: 10.1016/j.jhazmat.2014.01.024. Epub 2014 Jan 25.
A collective view of the degradation of monochlorocatechols in fungi is yet to be attained, though these compounds are recognised as key degradation intermediates of numerous chlorinated aromatic hydrocarbons, including monochlorophenols. In the present contribution we have analysed the degradation pathways of monochlorophenols in Aspergillus nidulans using essentially metabolomics. Degradation intermediates herein identified included those commonly reported (e.g. 3-chloro-cis,cis-muconate) but also compounds never reported before in fungi revealing for 4-chlorocatechol and for 3-chlorocatechol unknown degradation paths yielding 3-chlorodienelactone and catechol, respectively. A different 3-chlorocatechol degradation path led to accumulation of 2-chloromuconates (a potential dead-end), notwithstanding preliminary evidence of chloromuconolactones and protoanemonin simultaneous formation. In addition, some transformation intermediates, of which sulfate conjugates of mono-chlorophenols/chlorocatechols were the most common, were also identified. This study provides critical information for understanding the role of fungi in the degradation of chlorinated aromatic hydrocarbons; furthering their utility in the development of innovative bioremediation strategies.
真菌中单氯邻苯二酚降解的综合观点尚未形成,尽管这些化合物被认为是许多氯化芳烃,包括单氯酚的关键降解中间体。在本研究中,我们主要通过代谢组学分析了青霉属中(Aspergillus nidulans)单氯酚的降解途径。在此鉴定的降解中间产物包括那些常见的(例如 3-氯顺式,顺式-粘康酸),但也有从未在真菌中报道过的化合物,分别揭示了 4-氯邻苯二酚和 3-氯邻苯二酚的未知降解途径,分别生成 3-氯二烯内酯和儿茶酚。另一种不同的 3-氯邻苯二酚降解途径导致 2-氯粘康酸(潜在的死胡同)积累,尽管有初步证据表明同时形成了氯粘康酸内酯和原白头翁素。此外,还鉴定了一些转化中间产物,其中单氯酚/邻苯二酚的硫酸盐缀合物是最常见的。本研究为理解真菌在氯化芳烃降解中的作用提供了关键信息;进一步推动了它们在创新生物修复策略开发中的应用。