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Fabclavine diversity in Xenorhabdus bacteria
The global threat of multiresistant pathogens has to be answered by the development of novel antibiotics. Established antibiotic applications are often based on so-called secondary or specialized metabolites (SMs), identified in large screening approaches. To continue this successful strategy, new s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214866/ https://www.ncbi.nlm.nih.gov/pubmed/32461774 http://dx.doi.org/10.3762/bjoc.16.84 |
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author | Wenski, Sebastian L Cimen, Harun Berghaus, Natalie Fuchs, Sebastian W Hazir, Selcuk Bode, Helge B |
author_facet | Wenski, Sebastian L Cimen, Harun Berghaus, Natalie Fuchs, Sebastian W Hazir, Selcuk Bode, Helge B |
author_sort | Wenski, Sebastian L |
collection | PubMed |
description | The global threat of multiresistant pathogens has to be answered by the development of novel antibiotics. Established antibiotic applications are often based on so-called secondary or specialized metabolites (SMs), identified in large screening approaches. To continue this successful strategy, new sources for bioactive compounds are required, such as the bacterial genera Xenorhabdus or Photorhabdus. In these strains, fabclavines are widely distributed SMs with a broad-spectrum bioactivity. Fabclavines are hybrid SMs derived from nonribosomal peptide synthetases (NRPS), polyunsaturated fatty acid (PUFA), and polyketide synthases (PKS). Selected Xenorhabdus and Photorhabdus mutant strains were generated applying a chemically inducible promoter in front of the suggested fabclavine (fcl) biosynthesis gene cluster (BGC), followed by the analysis of the occurring fabclavines. Subsequently, known and unknown derivatives were identified and confirmed by MALDI–MS and MALDI–MS(2) experiments in combination with an optimized sample preparation. This led to a total number of 22 novel fabclavine derivatives in eight strains, increasing the overall number of fabclavines to 32. Together with the identification of fabclavines as major antibiotics in several entomopathogenic strains, our work lays the foundation for the rapid fabclavine identification and dereplication as the basis for future work of this widespread and bioactive SM class. |
format | Online Article Text |
id | pubmed-7214866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-72148662020-05-26 Fabclavine diversity in Xenorhabdus bacteria Wenski, Sebastian L Cimen, Harun Berghaus, Natalie Fuchs, Sebastian W Hazir, Selcuk Bode, Helge B Beilstein J Org Chem Full Research Paper The global threat of multiresistant pathogens has to be answered by the development of novel antibiotics. Established antibiotic applications are often based on so-called secondary or specialized metabolites (SMs), identified in large screening approaches. To continue this successful strategy, new sources for bioactive compounds are required, such as the bacterial genera Xenorhabdus or Photorhabdus. In these strains, fabclavines are widely distributed SMs with a broad-spectrum bioactivity. Fabclavines are hybrid SMs derived from nonribosomal peptide synthetases (NRPS), polyunsaturated fatty acid (PUFA), and polyketide synthases (PKS). Selected Xenorhabdus and Photorhabdus mutant strains were generated applying a chemically inducible promoter in front of the suggested fabclavine (fcl) biosynthesis gene cluster (BGC), followed by the analysis of the occurring fabclavines. Subsequently, known and unknown derivatives were identified and confirmed by MALDI–MS and MALDI–MS(2) experiments in combination with an optimized sample preparation. This led to a total number of 22 novel fabclavine derivatives in eight strains, increasing the overall number of fabclavines to 32. Together with the identification of fabclavines as major antibiotics in several entomopathogenic strains, our work lays the foundation for the rapid fabclavine identification and dereplication as the basis for future work of this widespread and bioactive SM class. Beilstein-Institut 2020-05-07 /pmc/articles/PMC7214866/ /pubmed/32461774 http://dx.doi.org/10.3762/bjoc.16.84 Text en Copyright © 2020, Wenski et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Wenski, Sebastian L Cimen, Harun Berghaus, Natalie Fuchs, Sebastian W Hazir, Selcuk Bode, Helge B Fabclavine diversity in Xenorhabdus bacteria |
title | Fabclavine diversity in Xenorhabdus bacteria |
title_full | Fabclavine diversity in Xenorhabdus bacteria |
title_fullStr | Fabclavine diversity in Xenorhabdus bacteria |
title_full_unstemmed | Fabclavine diversity in Xenorhabdus bacteria |
title_short | Fabclavine diversity in Xenorhabdus bacteria |
title_sort | fabclavine diversity in xenorhabdus bacteria |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214866/ https://www.ncbi.nlm.nih.gov/pubmed/32461774 http://dx.doi.org/10.3762/bjoc.16.84 |
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