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Intertwined Precursor Supply during Biosynthesis of the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76
[Image: see text] The explosive increase in genome sequencing and the advances in bioinformatic tools have revolutionized the rationale for natural product discovery from actinomycetes. In particular, this has revealed that actinomycete genomes contain numerous orphan gene clusters that have the pot...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696649/ https://www.ncbi.nlm.nih.gov/pubmed/28945067 http://dx.doi.org/10.1021/acschembio.7b00597 |
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author | Gubbens, Jacob Wu, Changsheng Zhu, Hua Filippov, Dmitri V. Florea, Bogdan I. Rigali, Sébastien Overkleeft, Herman S. van Wezel, Gilles P. |
author_facet | Gubbens, Jacob Wu, Changsheng Zhu, Hua Filippov, Dmitri V. Florea, Bogdan I. Rigali, Sébastien Overkleeft, Herman S. van Wezel, Gilles P. |
author_sort | Gubbens, Jacob |
collection | PubMed |
description | [Image: see text] The explosive increase in genome sequencing and the advances in bioinformatic tools have revolutionized the rationale for natural product discovery from actinomycetes. In particular, this has revealed that actinomycete genomes contain numerous orphan gene clusters that have the potential to specify many yet unknown bioactive specialized metabolites, representing a huge unexploited pool of chemical diversity. Here, we describe the discovery of a novel group of catecholate–hydroxamate siderophores termed qinichelins (2–5) from Streptomyces sp. MBT76. Correlation between the metabolite levels and the protein expression profiles identified the biosynthetic gene cluster (named qch) most likely responsible for qinichelin biosynthesis. The structure of the molecules was elucidated by bioinformatics, mass spectrometry, and NMR. The genome of Streptomyces sp. MBT76 contains three gene clusters for the production of catecholate–peptide siderophores, including a separate cluster for the production of a shared catecholate precursor. In addition, an operon in the qch cluster was identified for the production of the ornithine precursor for qinichelins, independent of primary metabolism. This biosynthetic complexity provides new insights into the challenges scientists face when applying synthetic biology approaches for natural product discovery. |
format | Online Article Text |
id | pubmed-5696649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56966492017-11-22 Intertwined Precursor Supply during Biosynthesis of the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 Gubbens, Jacob Wu, Changsheng Zhu, Hua Filippov, Dmitri V. Florea, Bogdan I. Rigali, Sébastien Overkleeft, Herman S. van Wezel, Gilles P. ACS Chem Biol [Image: see text] The explosive increase in genome sequencing and the advances in bioinformatic tools have revolutionized the rationale for natural product discovery from actinomycetes. In particular, this has revealed that actinomycete genomes contain numerous orphan gene clusters that have the potential to specify many yet unknown bioactive specialized metabolites, representing a huge unexploited pool of chemical diversity. Here, we describe the discovery of a novel group of catecholate–hydroxamate siderophores termed qinichelins (2–5) from Streptomyces sp. MBT76. Correlation between the metabolite levels and the protein expression profiles identified the biosynthetic gene cluster (named qch) most likely responsible for qinichelin biosynthesis. The structure of the molecules was elucidated by bioinformatics, mass spectrometry, and NMR. The genome of Streptomyces sp. MBT76 contains three gene clusters for the production of catecholate–peptide siderophores, including a separate cluster for the production of a shared catecholate precursor. In addition, an operon in the qch cluster was identified for the production of the ornithine precursor for qinichelins, independent of primary metabolism. This biosynthetic complexity provides new insights into the challenges scientists face when applying synthetic biology approaches for natural product discovery. American Chemical Society 2017-09-25 2017-11-17 /pmc/articles/PMC5696649/ /pubmed/28945067 http://dx.doi.org/10.1021/acschembio.7b00597 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Gubbens, Jacob Wu, Changsheng Zhu, Hua Filippov, Dmitri V. Florea, Bogdan I. Rigali, Sébastien Overkleeft, Herman S. van Wezel, Gilles P. Intertwined Precursor Supply during Biosynthesis of the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 |
title | Intertwined Precursor Supply during Biosynthesis of
the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 |
title_full | Intertwined Precursor Supply during Biosynthesis of
the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 |
title_fullStr | Intertwined Precursor Supply during Biosynthesis of
the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 |
title_full_unstemmed | Intertwined Precursor Supply during Biosynthesis of
the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 |
title_short | Intertwined Precursor Supply during Biosynthesis of
the Catecholate–Hydroxamate Siderophores Qinichelins in Streptomyces sp. MBT76 |
title_sort | intertwined precursor supply during biosynthesis of
the catecholate–hydroxamate siderophores qinichelins in streptomyces sp. mbt76 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696649/ https://www.ncbi.nlm.nih.gov/pubmed/28945067 http://dx.doi.org/10.1021/acschembio.7b00597 |
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