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Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction
Adaptation is normally viewed as the enemy of the antibiotic discovery and development process because adaptation among pathogens to antibiotic exposure leads to resistance. We present a method here that, in contrast, exploits the power of adaptation among antibiotic producers to accelerate the disc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312335/ https://www.ncbi.nlm.nih.gov/pubmed/22470465 http://dx.doi.org/10.1371/journal.pone.0033727 |
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author | Charusanti, Pep Fong, Nicole L. Nagarajan, Harish Pereira, Alban R. Li, Howard J. Abate, Elisa A. Su, Yongxuan Gerwick, William H. Palsson, Bernhard O. |
author_facet | Charusanti, Pep Fong, Nicole L. Nagarajan, Harish Pereira, Alban R. Li, Howard J. Abate, Elisa A. Su, Yongxuan Gerwick, William H. Palsson, Bernhard O. |
author_sort | Charusanti, Pep |
collection | PubMed |
description | Adaptation is normally viewed as the enemy of the antibiotic discovery and development process because adaptation among pathogens to antibiotic exposure leads to resistance. We present a method here that, in contrast, exploits the power of adaptation among antibiotic producers to accelerate the discovery of antibiotics. A competition-based adaptive laboratory evolution scheme is presented whereby an antibiotic-producing microorganism is competed against a target pathogen and serially passed over time until the producer evolves the ability to synthesize a chemical entity that inhibits growth of the pathogen. When multiple Streptomyces clavuligerus replicates were adaptively evolved against methicillin-resistant Staphylococcus aureus N315 in this manner, a strain emerged that acquired the ability to constitutively produce holomycin. In contrast, no holomycin could be detected from the unevolved wild-type strain. Moreover, genome re-sequencing revealed that the evolved strain had lost pSCL4, a large 1.8 Mbp plasmid, and acquired several single nucleotide polymorphisms in genes that have been shown to affect secondary metabolite biosynthesis. These results demonstrate that competition-based adaptive laboratory evolution can constitute a platform to create mutants that overproduce known antibiotics and possibly to discover new compounds as well. |
format | Online Article Text |
id | pubmed-3312335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33123352012-04-02 Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction Charusanti, Pep Fong, Nicole L. Nagarajan, Harish Pereira, Alban R. Li, Howard J. Abate, Elisa A. Su, Yongxuan Gerwick, William H. Palsson, Bernhard O. PLoS One Research Article Adaptation is normally viewed as the enemy of the antibiotic discovery and development process because adaptation among pathogens to antibiotic exposure leads to resistance. We present a method here that, in contrast, exploits the power of adaptation among antibiotic producers to accelerate the discovery of antibiotics. A competition-based adaptive laboratory evolution scheme is presented whereby an antibiotic-producing microorganism is competed against a target pathogen and serially passed over time until the producer evolves the ability to synthesize a chemical entity that inhibits growth of the pathogen. When multiple Streptomyces clavuligerus replicates were adaptively evolved against methicillin-resistant Staphylococcus aureus N315 in this manner, a strain emerged that acquired the ability to constitutively produce holomycin. In contrast, no holomycin could be detected from the unevolved wild-type strain. Moreover, genome re-sequencing revealed that the evolved strain had lost pSCL4, a large 1.8 Mbp plasmid, and acquired several single nucleotide polymorphisms in genes that have been shown to affect secondary metabolite biosynthesis. These results demonstrate that competition-based adaptive laboratory evolution can constitute a platform to create mutants that overproduce known antibiotics and possibly to discover new compounds as well. Public Library of Science 2012-03-21 /pmc/articles/PMC3312335/ /pubmed/22470465 http://dx.doi.org/10.1371/journal.pone.0033727 Text en Charusanti et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Charusanti, Pep Fong, Nicole L. Nagarajan, Harish Pereira, Alban R. Li, Howard J. Abate, Elisa A. Su, Yongxuan Gerwick, William H. Palsson, Bernhard O. Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction |
title | Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction |
title_full | Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction |
title_fullStr | Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction |
title_full_unstemmed | Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction |
title_short | Exploiting Adaptive Laboratory Evolution of Streptomyces clavuligerus for Antibiotic Discovery and Overproduction |
title_sort | exploiting adaptive laboratory evolution of streptomyces clavuligerus for antibiotic discovery and overproduction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312335/ https://www.ncbi.nlm.nih.gov/pubmed/22470465 http://dx.doi.org/10.1371/journal.pone.0033727 |
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