Identifying metabolic bottlenecks for micafungin precursor production via untargeted regulatory perturbation
Ping Men, Li Xie, Jiachen Wang, Yu Zhou, Xiaoxi Zhang, Yanping Li, Xuenian Huang, Xuefeng Lu

TL;DR
Researchers improved the production of the antifungal drug micafungin by identifying and addressing metabolic bottlenecks in its biosynthesis.
Contribution
A novel untargeted regulatory perturbation strategy was used to identify metabolic bottlenecks in micafungin precursor production.
Findings
Mutant library construction revealed diverse effects on FR901379 production, with some strains showing a 170% increase.
Transcriptome analysis showed upregulation of acetyl-CoA, palmitic acid, and 3′-phosphoadenosine-5′-phosphosulfate pathways in high-producing strains.
Exogenous palm oil supplementation increased FR901379 titer by 87.6%, highlighting the importance of precursor supply.
Abstract
Micafungin, a clinically important echinocandin antifungal agent, is derived from the nonribosomal cyclic hexapeptide FR901379 produced by the filamentous fungus Coleophoma empetri. However, low fermentation efficiency remains a major constraint in its industrial production. In this study, we implemented an untargeted regulatory perturbation strategy to systematically identify metabolic bottlenecks affecting FR901379 biosynthesis. A mutant library was constructed by rationally engineering the key untargeted regulatory genes involved in histone modification and global regulation. The untargeted perturbation led to diverse phenotypes in both growth and secondary metabolism, ranging from enhancement (by up to 170%) to complete abolition of FR901379 production. Transcriptome profiling of high-producing strains revealed coordinated upregulation of genes in the acetyl-CoA, palmitic acid, and…
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Taxonomy
TopicsMicrobial Natural Products and Biosynthesis · Plant biochemistry and biosynthesis · Enzyme Catalysis and Immobilization
