# Identifying metabolic bottlenecks for micafungin precursor production via untargeted regulatory perturbation

**Authors:** Ping Men, Li Xie, Jiachen Wang, Yu Zhou, Xiaoxi Zhang, Yanping Li, Xuenian Huang, Xuefeng Lu

PMC · DOI: 10.1186/s13068-026-02737-7 · 2026-01-14

## 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.

## Key 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 3′-phosphoadenosine-5′-phosphosulfate biosynthetic pathways. Exogenous supplementation of palm oil further enhanced FR901379 titer by 87.6%, confirming the critical role of precursor supply.

This work elucidates the metabolic network governing FR901379 biosynthesis and provides key candidates for further metabolic engineering. It also demonstrates that untargeted regulatory perturbation strategy is an effective approach for deciphering the mechanisms behind specific phenotypic traits in industrial filamentous fungi.

The online version contains supplementary material available at 10.1186/s13068-026-02737-7.

## Linked entities

- **Chemicals:** micafungin (PubChem CID 477468), FR901379 (PubChem CID 9876882), acetyl-CoA (PubChem CID 444493), palmitic acid (PubChem CID 985), 3′-phosphoadenosine-5′-phosphosulfate (PubChem CID 10214)
- **Species:** Coleophoma empetri (taxon 582885)

## Full-text entities

- **Diseases:** PAPS (MESH:D053307), IFIs (MESH:D000072742), fungal infections (MESH:D009181), APS (MESH:D016884), FPKM (MESH:D012892)
- **Chemicals:** amino acids (MESH:D000596), chloroisosulochrin (MESH:C562278), echinocandin (MESH:D054714), methanol (MESH:D000432), glucose (MESH:D005947), trifluoroacetic acid (MESH:D014269), nitrogen (MESH:D009584), fatty acid (MESH:D005227), CaCO3 (MESH:D002119), lovastatin (MESH:D008148), palm oil (MESH:D000073878), sulfur (MESH:D013455), sulfate (MESH:D013431), FR901379 (MESH:C110368), E2 (MESH:D004958), acetonitrile (MESH:C032159), cottonseed meal (MESH:D003369), CehdaA (-), APS (MESH:D000250), (NH4)2SO4 (MESH:D000645), pneumocandin B0 (MESH:C079465), corn starch (MESH:D013213), sucrose (MESH:D013395), D-sorbitol (MESH:D013012), Micafungin (MESH:D000077551), acid (MESH:D000143), 4-Aminobutanoic acid (MESH:D005680), Pentose phosphate (MESH:D010428), CaCl2 (MESH:D002122), ethanol (MESH:D000431), sulfide (MESH:D013440), acetate (MESH:D000085), penicillin (MESH:D010406), gliotoxin (MESH:D005912), Hygromycin B (MESH:D006921), water (MESH:D014867), palmitic acid (MESH:D019308), L-homotyrosine (MESH:C000711887), aflatoxin (MESH:D000348), methyl oleate (MESH:C005576), sterigmatocystin (MESH:D013241), terrequinone A. (MESH:C496935), Tricarboxylic acid (MESH:D014233), acetyl-CoA (MESH:D000105)
- **Species:** Aspergillus nidulans FGSC A4 (strain) [taxon 227321], Aspergillus fumigatus (species) [taxon 746128], Monascus purpureus (species) [taxon 5098], Calcarisporium arbuscula (species) [taxon 240499], Pestalotiopsis fici (species) [taxon 393283], Coleophoma empetri (species) [taxon 582885], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** MEFC10 — Mus musculus (Mouse), Hybridoma (CVCL_C4R4), MEFC09 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_VN68)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12874660/full.md

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Source: https://tomesphere.com/paper/PMC12874660