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Updated: May 12, 2026

Qualitative and Quantitative Analysis of Siderophore Production from Pseudomonas aeruginosa
Published on: March 15, 2024
Fungal siderophore biosynthesis is partially localized in peroxisomes
Mario Gründlinger1, Sabiha Yasmin, Beatrix Elisabeth Lechner
1Division of Molecular Biology/Biocenter, Innsbruck Medical University, Innrain 80-82, A-6020, Innsbruck, Austria.
Abstract:
Siderophores play a central role in iron metabolism and virulence of most fungi. Both Aspergillus fumigatus and Aspergillus nidulans excrete the siderophore triacetylfusarinine C (TAFC) for iron acquisition. In A. fumigatus, green fluorescence protein-tagging revealed peroxisomal localization of the TAFC biosynthetic enzymes SidI (mevalonyl-CoA ligase), SidH (mevalonyl-CoA hydratase) and SidF (anhydromevalonyl-CoA transferase), while elimination of the peroxisomal targeting signal (PTS) impaired both, peroxisomal SidH-targeting and TAFC biosynthesis. The analysis of A. nidulans mutants deficient in peroxisomal biogenesis, ATP import or protein import revealed that cytosolic mislocalization of one or two but, interestingly, not all three enzymes impairs TAFC production during iron starvation. The PTS motifs are conserved in fungal orthologues of SidF, SidH and SidI. In agreement with the evolutionary conservation of the partial peroxisomal compartmentalization of fungal siderophore biosynthesis, the SidI orthologue of coprogen-type siderophore-producing Neurospora crassa was confirmed to be peroxisomal. Taken together, this study identified and characterized a novel, evolutionary conserved metabolic function of peroxisomes.
Insights
Fungal siderophore biosynthesis, crucial for iron acquisition, is localized to peroxisomes. This study reveals conserved peroxisomal targeting signals in key enzymes, highlighting a novel metabolic role for peroxisomes in fungi.
Area of Science:
- Biochemistry
- Mycology
- Cell Biology
Background:
- Siderophores are essential for iron metabolism and fungal virulence.
- Aspergillus fumigatus and Aspergillus nidulans utilize triacetylfusarinine C (TAFC) for iron acquisition.
Purpose of the Study:
- To investigate the role of peroxisomes in fungal siderophore biosynthesis.
- To identify and characterize the localization and function of TAFC biosynthetic enzymes.
Main Methods:
- Green fluorescence protein (GFP)-tagging of TAFC biosynthetic enzymes (SidI, SidH, SidF) in Aspergillus fumigatus.
- Analysis of Aspergillus nidulans mutants deficient in peroxisomal biogenesis, ATP import, or protein import.
- Bioinformatic analysis of conserved peroxisomal targeting signals (PTS) in fungal siderophore biosynthetic enzymes.
Main Results:
- TAFC biosynthetic enzymes SidI, SidH, and SidF were localized to peroxisomes in Aspergillus fumigatus.
- Elimination of peroxisomal targeting signals impaired enzyme localization and TAFC biosynthesis.
- Cytosolic mislocalization of TAFC enzymes in Aspergillus nidulans mutants impaired TAFC production.
- Conserved PTS motifs were identified in fungal orthologues of SidF, SidH, and SidI.
- The SidI orthologue in Neurospora crassa was also confirmed to be peroxisomal.
Conclusions:
- This study identifies a novel, evolutionarily conserved metabolic function of peroxisomes in fungal siderophore biosynthesis.
- Peroxisomal compartmentalization of TAFC biosynthesis is crucial for iron acquisition in fungi.
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