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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...

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Autores principales: Charusanti, Pep, Fong, Nicole L., Nagarajan, Harish, Pereira, Alban R., Li, Howard J., Abate, Elisa A., Su, Yongxuan, Gerwick, William H., Palsson, Bernhard O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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