Regulatory networks governing methionine catabolism into volatile organic sulfur-containing compounds in Clonostachys rosea .

Adaptation to environmental perturbations requires living systems to coordinately regulate signaling pathways, gene expression and metabolism. To better understand the mechanisms underlying adaptation, the regulatory nodes within networks must be elucidated. Here, ARO8-2, which encodes an aminotransferase; PDC , which encodes a decarboxylase; and STR3 , which encodes a demethiolase, were identified as key genes involved in the catabolism of methionine (Met) in the mycoparasitic fungus Clonostachys rosea isolated from Tuber melanosporum ascocarps. Exogenous Met induced the transcription of ARO8-2 and PDC but repressed the transcription of STR3 , which is controlled by the putative binding sites of MSN2 and GLN3 responding to nitrogen catabolite repression. Met and its structural derivatives function as glutamine synthetase inhibitors, resulting in the downregulation of STR3 expression. The putative GLN3 binding site was necessary for STR3 downregulation. In Saccharomyces cerevisiae , Met and its structural derivatives also triggered downregulation of demethiolase gene expression. Altogether, the results indicated that exogenous Met triggered nitrogen catabolite repression, which stimulated the Ehrlich pathway and negatively regulated the demethiolation pathway via the methionine sulfoximine-responsive regulatory pathway. This finding revealed the regulatory nodes within the networks controlling the catabolism of Met into volatile organic sulfur-containing compounds, thereby enhancing our understanding of adaptation. IMPORTANCE Methionine (Met) shuttles organic nitrogen and plays a central role in nitrogen metabolism. Exogenous Met strongly induces the expression of ARO8-2 and PDC , represses the expression of STR3 and generates volatile organic sulfur-containing compounds (VOSCs) via the Ehrlich and demethiolation pathways. In this study, we used genetic, bioinformatic and metabolite-based analyses to confirm that transcriptional control of the aminotransferase gene ARO8-2 , the decarboxylase gene PDC and the demethiolase gene STR3 modulates Met catabolism into VOSCs. Importantly, we found that in addition to the Ehrlich pathway, the demethiolation pathway was also regulated by a nitrogen catabolite repression-sensitive regulatory pathway that controlled the transcription of genes required to catabolize poor nitrogen sources. This work significantly advances our understanding of nitrogen catabolite repression-sensitive transcriptional regulation of sulfur-containing amino acid catabolism and provides a basis for engineering Met catabolic pathways for the production of fuel and valuable flavor alcohols.