Atrazine is one of the most widespread chlorinated herbicides, leaving large bulks in soils and groundwater. The metabolic pathways of biodegradation of atrazine by bacteria are well described, but many aspects of the fungal biodegradation of this compound remain unclear. Thus, we investigated the toxicity and degradation of atrazine by 13 rainforest basidiomycete strains. In liquid medium, Pluteus cubensis SXS320, Gloelophyllum striatum MCA7, and Agaricales MCA17 removed 30, 37, and 38%, respectively, of initial 25 mg L -1 of herbicide within 20 days. Deficiency of nitrogen drove atrazine degradation by Pluteus cubensis SXS320; this strain removed 30% of atrazine within 20 days in a culture medium with 2.5mM of N, raising three metabolites; in a medium with 25mM of N, only 21% of initial atrazine were removed after 40 days, and two metabolites appeared in culture extracts. This is the first report of such different outcomes linked to nitrogen availability during the biodegradation of atrazine by basidiomycetes. The herbicide also induced synthesis and secretion of extracellular laccases by Datronia caperata MCA5, Pycnoporus sanguineus MCA16, and Polyporus tenuiculus MCA11. Laccase levels in contaminated medium of P. tenuiculus MCA11 were 13.3-fold superior than in control; the possible role on this enzyme on atrazine biodegradation was evaluated, considering the strong induction and the removal of 13.9% of the herbicide in vivo . Although 88% of initial laccase activity remained after 6h, no evidence of in vitro degradation was observed, even though ABTS was present as mediator. Further studies, including a full characterization of the metabolites obtained, are desirable to assess the security of the use of these strains as in situ bioremediation tools. The search for other ligninolytic extracellular enzymes and cell-bound mechanisms implicated on the degradation would enlightens key aspects of the role of nitrogen in atrazine metabolism by basidiomycetes.