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Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent

Antibiotic-producing microbes evolved self-resistance mechanisms to avoid suicide. The biocontrol Agrobacterium radiobacter K84 secretes the Trojan Horse antibiotic agrocin 84 that is selectively transported into the plant pathogen A. tumefaciens and processed into the toxin TM84. We previously show...

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Autores principales: Chopra, Shaileja, Palencia, Andrés, Virus, Cornelia, Schulwitz, Sarah, Temple, Brenda R., Cusack, Stephen, Reader, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059758/
https://www.ncbi.nlm.nih.gov/pubmed/27713402
http://dx.doi.org/10.1038/ncomms12928
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author Chopra, Shaileja
Palencia, Andrés
Virus, Cornelia
Schulwitz, Sarah
Temple, Brenda R.
Cusack, Stephen
Reader, John
author_facet Chopra, Shaileja
Palencia, Andrés
Virus, Cornelia
Schulwitz, Sarah
Temple, Brenda R.
Cusack, Stephen
Reader, John
author_sort Chopra, Shaileja
collection PubMed
description Antibiotic-producing microbes evolved self-resistance mechanisms to avoid suicide. The biocontrol Agrobacterium radiobacter K84 secretes the Trojan Horse antibiotic agrocin 84 that is selectively transported into the plant pathogen A. tumefaciens and processed into the toxin TM84. We previously showed that TM84 employs a unique tRNA-dependent mechanism to inhibit leucyl-tRNA synthetase (LeuRS), while the TM84-producer prevents self-poisoning by expressing a resistant LeuRS AgnB2. We now identify a mechanism by which the antibiotic-producing microbe resists its own toxin. Using a combination of structural, biochemical and biophysical approaches, we show that AgnB2 evolved structural changes so as to resist the antibiotic by eliminating the tRNA-dependence of TM84 binding. Mutagenesis of key resistance determinants results in mutants adopting an antibiotic-sensitive phenotype. This study illuminates the evolution of resistance in self-immunity genes and provides mechanistic insights into a fascinating tRNA-dependent antibiotic with applications for the development of anti-infectives and the prevention of biocontrol emasculation.
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spelling pubmed-50597582016-10-26 Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent Chopra, Shaileja Palencia, Andrés Virus, Cornelia Schulwitz, Sarah Temple, Brenda R. Cusack, Stephen Reader, John Nat Commun Article Antibiotic-producing microbes evolved self-resistance mechanisms to avoid suicide. The biocontrol Agrobacterium radiobacter K84 secretes the Trojan Horse antibiotic agrocin 84 that is selectively transported into the plant pathogen A. tumefaciens and processed into the toxin TM84. We previously showed that TM84 employs a unique tRNA-dependent mechanism to inhibit leucyl-tRNA synthetase (LeuRS), while the TM84-producer prevents self-poisoning by expressing a resistant LeuRS AgnB2. We now identify a mechanism by which the antibiotic-producing microbe resists its own toxin. Using a combination of structural, biochemical and biophysical approaches, we show that AgnB2 evolved structural changes so as to resist the antibiotic by eliminating the tRNA-dependence of TM84 binding. Mutagenesis of key resistance determinants results in mutants adopting an antibiotic-sensitive phenotype. This study illuminates the evolution of resistance in self-immunity genes and provides mechanistic insights into a fascinating tRNA-dependent antibiotic with applications for the development of anti-infectives and the prevention of biocontrol emasculation. Nature Publishing Group 2016-10-07 /pmc/articles/PMC5059758/ /pubmed/27713402 http://dx.doi.org/10.1038/ncomms12928 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chopra, Shaileja
Palencia, Andrés
Virus, Cornelia
Schulwitz, Sarah
Temple, Brenda R.
Cusack, Stephen
Reader, John
Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent
title Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent
title_full Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent
title_fullStr Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent
title_full_unstemmed Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent
title_short Structural characterization of antibiotic self-immunity tRNA synthetase in plant tumour biocontrol agent
title_sort structural characterization of antibiotic self-immunity trna synthetase in plant tumour biocontrol agent
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059758/
https://www.ncbi.nlm.nih.gov/pubmed/27713402
http://dx.doi.org/10.1038/ncomms12928
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