Cargando…

Fungal siderophore biosynthesis is partially localized in peroxisomes

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gründlinger, Mario, Yasmin, Sabiha, Lechner, Beatrix Elisabeth, Geley, Stephan, Schrettl, Markus, Hynes, Michael, Haas, Hubertus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709128/
https://www.ncbi.nlm.nih.gov/pubmed/23617799
http://dx.doi.org/10.1111/mmi.12225
_version_ 1782276711186956288
author Gründlinger, Mario
Yasmin, Sabiha
Lechner, Beatrix Elisabeth
Geley, Stephan
Schrettl, Markus
Hynes, Michael
Haas, Hubertus
author_facet Gründlinger, Mario
Yasmin, Sabiha
Lechner, Beatrix Elisabeth
Geley, Stephan
Schrettl, Markus
Hynes, Michael
Haas, Hubertus
author_sort Gründlinger, Mario
collection PubMed
description 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.
format Online
Article
Text
id pubmed-3709128
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-37091282013-08-05 Fungal siderophore biosynthesis is partially localized in peroxisomes Gründlinger, Mario Yasmin, Sabiha Lechner, Beatrix Elisabeth Geley, Stephan Schrettl, Markus Hynes, Michael Haas, Hubertus Mol Microbiol Research Articles 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. Blackwell Publishing Ltd 2013-06 2013-04-26 /pmc/articles/PMC3709128/ /pubmed/23617799 http://dx.doi.org/10.1111/mmi.12225 Text en Copyright © 2013 John Wiley & Sons Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research Articles
Gründlinger, Mario
Yasmin, Sabiha
Lechner, Beatrix Elisabeth
Geley, Stephan
Schrettl, Markus
Hynes, Michael
Haas, Hubertus
Fungal siderophore biosynthesis is partially localized in peroxisomes
title Fungal siderophore biosynthesis is partially localized in peroxisomes
title_full Fungal siderophore biosynthesis is partially localized in peroxisomes
title_fullStr Fungal siderophore biosynthesis is partially localized in peroxisomes
title_full_unstemmed Fungal siderophore biosynthesis is partially localized in peroxisomes
title_short Fungal siderophore biosynthesis is partially localized in peroxisomes
title_sort fungal siderophore biosynthesis is partially localized in peroxisomes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709128/
https://www.ncbi.nlm.nih.gov/pubmed/23617799
http://dx.doi.org/10.1111/mmi.12225
work_keys_str_mv AT grundlingermario fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes
AT yasminsabiha fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes
AT lechnerbeatrixelisabeth fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes
AT geleystephan fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes
AT schrettlmarkus fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes
AT hynesmichael fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes
AT haashubertus fungalsiderophorebiosynthesisispartiallylocalizedinperoxisomes