Deciphering the role of Th HSF1 in the differential expression regulation of laccase isozymes in the white-rot fungus Trametes hirsuta

作者：Kun Wu, Rong Zhu, Shiwen Zhao, Chenkai Wang, Xinlei Zhang, Shenglong Liu, Zemin Fang, Yazhong Xiao, Juanjuan Liu · 发表于：Microbiology Spectrum · 年份：2025 · DOI：10.1128/spectrum.01004-25 · 被引用次数：1 · 研究领域：Enzyme-mediated dye degradation、Fungal and yeast genetics research、melanin and skin pigmentation

ABSTRACT White-rot fungi exhibit responses to Cu 2+ , leading to a substantial increase in the production of certain laccase isozymes for industry utilization. Currently, studies on the differential expression mechanism of the laccase isozymes in white-rot fungi are limited. Three laccase isozymes, LacA, LacB, and LacF, were significantly induced in Trametes hirsuta AH28-2 when exposed to Cu 2+ , accompanied by a slight enhancement in the isozyme LacC level. Here, based on transcriptomics and proteomics, a nuclear-localized heat shock transcription factor, Th HSF1, was mined and exhibited as a copper-responsive protein involved in the differential regulation of laccase isozyme expression. A changed colony morphology and curved hyphal morphology were observed in three Thhsf1 -silenced T. hirsuta AH28-2 transformants in response to Cu 2+ stress. Thhsf1 silencing resulted in downregulated transcriptional levels and activities of LacA, LacB, and LacF, but not LacC. EMSA assays further demonstrated the binding of Th HSF1 only to the promoter regions of lacA , lacB, and lacF containing HSE elements like CTTGAA. A previously reported Hsp70 homolog, Th HspA1, could interact with Th HSF1 and synergistically regulate the expressions of three laccase isozymes. Th HSF1 and Th HspA1 co-overexpression led to approximately 1.5-fold increased laccase activities, providing an efficient strategy to enhance laccase production. IMPORTANCE White-rot fungi, especially Trametes species, are importa...