A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.

The filamentous fungus Penicillium chrysogenum harbors an astonishing variety of nonribosomal peptide synthetase genes, which encode proteins known to produce complex bioactive metabolites from simple building blocks. Here we report a novel non-canonical tetra-modular nonribosomal peptide synthetase...

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Main Authors: Hazrat Ali, Marco I Ries, Peter P Lankhorst, Rob A M van der Hoeven, Olaf L Schouten, Marek Noga, Thomas Hankemeier, Noël N M E van Peij, Roel A L Bovenberg, Rob J Vreeken, Arnold J M Driessen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24887561/pdf/?tool=EBI
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spelling doaj-6380c87e856c4595a25ae2fd2cea9b992021-03-04T09:22:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0196e9821210.1371/journal.pone.0098212A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.Hazrat AliMarco I RiesPeter P LankhorstRob A M van der HoevenOlaf L SchoutenMarek NogaThomas HankemeierNoël N M E van PeijRoel A L BovenbergRob J VreekenArnold J M DriessenThe filamentous fungus Penicillium chrysogenum harbors an astonishing variety of nonribosomal peptide synthetase genes, which encode proteins known to produce complex bioactive metabolites from simple building blocks. Here we report a novel non-canonical tetra-modular nonribosomal peptide synthetase (NRPS) with microheterogenicity of all involved adenylation domains towards their respective substrates. By deleting the putative gene in combination with comparative metabolite profiling various unique cyclic and derived linear tetrapeptides were identified which were associated with this NRPS, including fungisporin. In combination with substrate predictions for each module, we propose a mechanism for a 'trans-acting' adenylation domain.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24887561/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Hazrat Ali
Marco I Ries
Peter P Lankhorst
Rob A M van der Hoeven
Olaf L Schouten
Marek Noga
Thomas Hankemeier
Noël N M E van Peij
Roel A L Bovenberg
Rob J Vreeken
Arnold J M Driessen
spellingShingle Hazrat Ali
Marco I Ries
Peter P Lankhorst
Rob A M van der Hoeven
Olaf L Schouten
Marek Noga
Thomas Hankemeier
Noël N M E van Peij
Roel A L Bovenberg
Rob J Vreeken
Arnold J M Driessen
A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.
PLoS ONE
author_facet Hazrat Ali
Marco I Ries
Peter P Lankhorst
Rob A M van der Hoeven
Olaf L Schouten
Marek Noga
Thomas Hankemeier
Noël N M E van Peij
Roel A L Bovenberg
Rob J Vreeken
Arnold J M Driessen
author_sort Hazrat Ali
title A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.
title_short A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.
title_full A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.
title_fullStr A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.
title_full_unstemmed A non-canonical NRPS is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in Penicillium chrysogenum.
title_sort non-canonical nrps is involved in the synthesis of fungisporin and related hydrophobic cyclic tetrapeptides in penicillium chrysogenum.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description The filamentous fungus Penicillium chrysogenum harbors an astonishing variety of nonribosomal peptide synthetase genes, which encode proteins known to produce complex bioactive metabolites from simple building blocks. Here we report a novel non-canonical tetra-modular nonribosomal peptide synthetase (NRPS) with microheterogenicity of all involved adenylation domains towards their respective substrates. By deleting the putative gene in combination with comparative metabolite profiling various unique cyclic and derived linear tetrapeptides were identified which were associated with this NRPS, including fungisporin. In combination with substrate predictions for each module, we propose a mechanism for a 'trans-acting' adenylation domain.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24887561/pdf/?tool=EBI
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