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Genomic-Led Discovery of a Novel Glycopeptide Antibiotic by Nonomuraea coxensis DSM 45129
[Image: see text] Glycopeptide antibiotics (GPAs) are last defense line drugs against multidrug-resistant Gram-positive pathogens. Natural GPAs teicoplanin and vancomycin, as well as semisynthetic oritavancin, telavancin, and dalbavancin, are currently approved for clinical use. Although these antib...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291499/ https://www.ncbi.nlm.nih.gov/pubmed/33913701 http://dx.doi.org/10.1021/acschembio.1c00170 |
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author | Yushchuk, Oleksandr Vior, Natalia M. Andreo-Vidal, Andres Berini, Francesca Rückert, Christian Busche, Tobias Binda, Elisa Kalinowski, Jörn Truman, Andrew W. Marinelli, Flavia |
author_facet | Yushchuk, Oleksandr Vior, Natalia M. Andreo-Vidal, Andres Berini, Francesca Rückert, Christian Busche, Tobias Binda, Elisa Kalinowski, Jörn Truman, Andrew W. Marinelli, Flavia |
author_sort | Yushchuk, Oleksandr |
collection | PubMed |
description | [Image: see text] Glycopeptide antibiotics (GPAs) are last defense line drugs against multidrug-resistant Gram-positive pathogens. Natural GPAs teicoplanin and vancomycin, as well as semisynthetic oritavancin, telavancin, and dalbavancin, are currently approved for clinical use. Although these antibiotics remain efficient, emergence of novel GPA-resistant pathogens is a question of time. Therefore, it is important to investigate the natural variety of GPAs coming from so-called “rare” actinobacteria. Herein we describe a novel GPA producer—Nonomuraea coxensis DSM 45129. Its de novo sequenced and completely assembled genome harbors a biosynthetic gene cluster (BGC) similar to the dbv BGC of A40926, the natural precursor to dalbavancin. The strain produces a novel GPA, which we propose is an A40926 analogue lacking the carboxyl group on the N-acylglucosamine moiety. This structural difference correlates with the absence of dbv29—coding for an enzyme responsible for the oxidation of the N-acylglucosamine moiety. Introduction of dbv29 into N. coxensis led to A40926 production in this strain. Finally, we successfully applied dbv3 and dbv4 heterologous transcriptional regulators to trigger and improve A50926 production in N. coxensis, making them prospective tools for screening other Nonomuraea spp. for GPA production. Our work highlights genus Nonomuraea as a still untapped source of novel GPAs. |
format | Online Article Text |
id | pubmed-8291499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82914992021-07-21 Genomic-Led Discovery of a Novel Glycopeptide Antibiotic by Nonomuraea coxensis DSM 45129 Yushchuk, Oleksandr Vior, Natalia M. Andreo-Vidal, Andres Berini, Francesca Rückert, Christian Busche, Tobias Binda, Elisa Kalinowski, Jörn Truman, Andrew W. Marinelli, Flavia ACS Chem Biol [Image: see text] Glycopeptide antibiotics (GPAs) are last defense line drugs against multidrug-resistant Gram-positive pathogens. Natural GPAs teicoplanin and vancomycin, as well as semisynthetic oritavancin, telavancin, and dalbavancin, are currently approved for clinical use. Although these antibiotics remain efficient, emergence of novel GPA-resistant pathogens is a question of time. Therefore, it is important to investigate the natural variety of GPAs coming from so-called “rare” actinobacteria. Herein we describe a novel GPA producer—Nonomuraea coxensis DSM 45129. Its de novo sequenced and completely assembled genome harbors a biosynthetic gene cluster (BGC) similar to the dbv BGC of A40926, the natural precursor to dalbavancin. The strain produces a novel GPA, which we propose is an A40926 analogue lacking the carboxyl group on the N-acylglucosamine moiety. This structural difference correlates with the absence of dbv29—coding for an enzyme responsible for the oxidation of the N-acylglucosamine moiety. Introduction of dbv29 into N. coxensis led to A40926 production in this strain. Finally, we successfully applied dbv3 and dbv4 heterologous transcriptional regulators to trigger and improve A50926 production in N. coxensis, making them prospective tools for screening other Nonomuraea spp. for GPA production. Our work highlights genus Nonomuraea as a still untapped source of novel GPAs. American Chemical Society 2021-04-29 2021-05-21 /pmc/articles/PMC8291499/ /pubmed/33913701 http://dx.doi.org/10.1021/acschembio.1c00170 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Yushchuk, Oleksandr Vior, Natalia M. Andreo-Vidal, Andres Berini, Francesca Rückert, Christian Busche, Tobias Binda, Elisa Kalinowski, Jörn Truman, Andrew W. Marinelli, Flavia Genomic-Led Discovery of a Novel Glycopeptide Antibiotic by Nonomuraea coxensis DSM 45129 |
title | Genomic-Led Discovery of a Novel Glycopeptide Antibiotic
by Nonomuraea coxensis DSM 45129 |
title_full | Genomic-Led Discovery of a Novel Glycopeptide Antibiotic
by Nonomuraea coxensis DSM 45129 |
title_fullStr | Genomic-Led Discovery of a Novel Glycopeptide Antibiotic
by Nonomuraea coxensis DSM 45129 |
title_full_unstemmed | Genomic-Led Discovery of a Novel Glycopeptide Antibiotic
by Nonomuraea coxensis DSM 45129 |
title_short | Genomic-Led Discovery of a Novel Glycopeptide Antibiotic
by Nonomuraea coxensis DSM 45129 |
title_sort | genomic-led discovery of a novel glycopeptide antibiotic
by nonomuraea coxensis dsm 45129 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291499/ https://www.ncbi.nlm.nih.gov/pubmed/33913701 http://dx.doi.org/10.1021/acschembio.1c00170 |
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