Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782459472243851264 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5059758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT choprashaileja structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent AT palenciaandres structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent AT viruscornelia structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent AT schulwitzsarah structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent AT templebrendar structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent AT cusackstephen structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent AT readerjohn structuralcharacterizationofantibioticselfimmunitytrnasynthetaseinplanttumourbiocontrolagent |