数字农科院2.0

The pH-responsive regulator PlPacC and GATA transcription factor PlAreB are involved in the regulation of the biosynthesis of the antifungal lipopeptaibols leucinostatins in Purpureocillium lilacinum

文献类型： 外文期刊

作者： Zixin Li;Yang Jiao;Jiawei Tang;Xin Dong;Romain Thomas;Bingyan Xie;Yan Li;Philippe Jacques

作者机构：

关键词： AreB;CRISPR-Cas9;Leucinostatins;PacC;PDB;Purpureocillium lilacinum

期刊名称： Microbiological Research

ISSN： 0944-5013

年卷期： 2025 年 302 卷

页码：

收录情况： SCIE（2025版） ; ; EI（2025版）

摘要： The biocontrol fungus Purpureocillium lilacinum PLBJ-1 produces leucinostatins, a class of non-ribosomal peptides (NRPs) with broad-spectrum antimicrobial activities. However, the molecular mechanisms underlying the optimization of culture conditions for leucinostatin production remain unexplored. Previous research showed that PLBJ-1 synthesizes leucinostatins more effectively in hand-made Potato Dextrose Broth (PDB-M) than in commercially available PDB (PDB-C). Elementary analysis of these two media indicated that the difference in leucinostatin yield was correlated with variations in pH dynamics and nitrogen content. Subsequent experiments under different initial pH and nitrogen levels confirmed that an alkaline environment and reduced nitrogen availability could enhance leucinostatin production. To investigate the regulators involved, CRISPR-Cas9-mediated gene disruptions were performed on the pH-responsive transcription factor PlPacC and the nitrogen regulator PlAreB. The disruption of either PlPacC or PlAreB resulted in a marked reduction in biomass and sporulation in P. lilacinum PLBJ-1. Specifically, PlPacC disruption impaired environmental pH regulation and significantly decreased leucinostatin production. In contrast, PlAreB disruption led to an increased leucinostatin yield. Overall, these findings demonstrate that environmental pH and nitrogen availability are the critical factors governing leucinostatin biosynthesis, acting through two key transcriptional regulators, PlPacC and PlAreB. This study lays a molecular foundation for future large-scale optimization of leucinostatin fermentation.

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