A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore

The model white-rot basidiomycete Ceriporiopsis (Gelatoporia) subvermispora B encodes putative natural product biosynthesis genes. Among them is the gene for the seven-domain nonribosomal peptide synthetase CsNPS2. It is a member of the as-yet uncharacterized fungal type VI siderophore synthetase fa...

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Main Authors: Brandenburger, Eileen, Gressler, Markus, Leonhardt, Robin, Lackner, Gerald, Habel, Andreas, Hertweck, Christian, Brock, Matthias, Hoffmeister, Dirk
Format: Article
Published: American Society for Microbiology 2017
Online Access:https://eprints.nottingham.ac.uk/45543/
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author Brandenburger, Eileen
Gressler, Markus
Leonhardt, Robin
Lackner, Gerald
Habel, Andreas
Hertweck, Christian
Brock, Matthias
Hoffmeister, Dirk
author_facet Brandenburger, Eileen
Gressler, Markus
Leonhardt, Robin
Lackner, Gerald
Habel, Andreas
Hertweck, Christian
Brock, Matthias
Hoffmeister, Dirk
author_sort Brandenburger, Eileen
building Nottingham Research Data Repository
collection Online Access
description The model white-rot basidiomycete Ceriporiopsis (Gelatoporia) subvermispora B encodes putative natural product biosynthesis genes. Among them is the gene for the seven-domain nonribosomal peptide synthetase CsNPS2. It is a member of the as-yet uncharacterized fungal type VI siderophore synthetase family which is highly conserved and widely distributed among the basidiomycetes. These enzymes include only one adenylation (A) domain, i.e., one complete peptide synthetase module and two thiolation/condensation (T-C) di-domain partial modules which, together, constitute an AT1C1T2C2T3C3 domain setup. The full-length CsNPS2 enzyme (274.5 kDa) was heterologously produced as polyhistidine fusion in Aspergillus niger as soluble and active protein. N5-acetyl-N5-hydroxy-L-ornithine (L-AHO) and N5-cis anhydromevalonyl-N5-hydroxy-L-ornithine (L-AMHO) were accepted as substrates, as assessed in vitro using the substrate-dependent [32P] ATP-pyrophosphate radioisotope exchange assay. Full-length holo-CsNPS2 catalyzed amide bond formation between three L-AHO molecules to release the linear L-AHO trimer, called basidioferrin, as product in vitro, which was verified by LC-HRESIMS. Phylogenetic analyses suggest that type VI family siderophore synthetases are widespread in mushrooms and have evolved in a common ancestor of basidiomycetes.
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spelling nottingham-455432020-05-04T19:02:17Z https://eprints.nottingham.ac.uk/45543/ A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore Brandenburger, Eileen Gressler, Markus Leonhardt, Robin Lackner, Gerald Habel, Andreas Hertweck, Christian Brock, Matthias Hoffmeister, Dirk The model white-rot basidiomycete Ceriporiopsis (Gelatoporia) subvermispora B encodes putative natural product biosynthesis genes. Among them is the gene for the seven-domain nonribosomal peptide synthetase CsNPS2. It is a member of the as-yet uncharacterized fungal type VI siderophore synthetase family which is highly conserved and widely distributed among the basidiomycetes. These enzymes include only one adenylation (A) domain, i.e., one complete peptide synthetase module and two thiolation/condensation (T-C) di-domain partial modules which, together, constitute an AT1C1T2C2T3C3 domain setup. The full-length CsNPS2 enzyme (274.5 kDa) was heterologously produced as polyhistidine fusion in Aspergillus niger as soluble and active protein. N5-acetyl-N5-hydroxy-L-ornithine (L-AHO) and N5-cis anhydromevalonyl-N5-hydroxy-L-ornithine (L-AMHO) were accepted as substrates, as assessed in vitro using the substrate-dependent [32P] ATP-pyrophosphate radioisotope exchange assay. Full-length holo-CsNPS2 catalyzed amide bond formation between three L-AHO molecules to release the linear L-AHO trimer, called basidioferrin, as product in vitro, which was verified by LC-HRESIMS. Phylogenetic analyses suggest that type VI family siderophore synthetases are widespread in mushrooms and have evolved in a common ancestor of basidiomycetes. American Society for Microbiology 2017-08-25 Article PeerReviewed Brandenburger, Eileen, Gressler, Markus, Leonhardt, Robin, Lackner, Gerald, Habel, Andreas, Hertweck, Christian, Brock, Matthias and Hoffmeister, Dirk (2017) A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore. Applied and Environmental Microbiology . ISSN 0099-2240 http://aem.asm.org/content/early/2017/08/21/AEM.01478-17 doi:10.1128/AEM.01478-17 doi:10.1128/AEM.01478-17
spellingShingle Brandenburger, Eileen
Gressler, Markus
Leonhardt, Robin
Lackner, Gerald
Habel, Andreas
Hertweck, Christian
Brock, Matthias
Hoffmeister, Dirk
A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
title A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
title_full A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
title_fullStr A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
title_full_unstemmed A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
title_short A highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
title_sort highly conserved basidiomycete peptide synthetase produces a trimeric hydroxamate siderophore
url https://eprints.nottingham.ac.uk/45543/
https://eprints.nottingham.ac.uk/45543/
https://eprints.nottingham.ac.uk/45543/