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S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC
Microcin C (McC)-like compounds are natural Trojan horse peptide-nucleotide antibiotics produced by diverse bacteria. The ribosomally synthesized peptide parts of these antibiotics are responsible for their facilitated transport into susceptible cells. Once inside the cell, the peptide part is degra...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239234/ https://www.ncbi.nlm.nih.gov/pubmed/35467414 http://dx.doi.org/10.1128/mbio.00805-22 |
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author | Yagmurov, Eldar Gilep, Konstantin Serebryakova, Marina Wolf, Yuri I. Dubiley, Svetlana Severinov, Konstantin |
author_facet | Yagmurov, Eldar Gilep, Konstantin Serebryakova, Marina Wolf, Yuri I. Dubiley, Svetlana Severinov, Konstantin |
author_sort | Yagmurov, Eldar |
collection | PubMed |
description | Microcin C (McC)-like compounds are natural Trojan horse peptide-nucleotide antibiotics produced by diverse bacteria. The ribosomally synthesized peptide parts of these antibiotics are responsible for their facilitated transport into susceptible cells. Once inside the cell, the peptide part is degraded, releasing the toxic payload, an isoaspartyl-nucleotide that inhibits aspartyl-tRNA synthetase, an enzyme essential for protein synthesis. Bacteria that produce microcin C-like compounds have evolved multiple ways to avoid self-intoxication. Here, we describe a new strategy through the action of S51 family peptidases, which we name MccG. MccG cleaves the toxic isoaspartyl-nucleotide, rendering it inactive. While some MccG homologs are encoded by gene clusters responsible for biosynthesis of McC-like compounds, most are encoded by standalone genes whose products may provide a basal level of resistance to peptide-nucleotide antibiotics in phylogenetically distant bacteria. |
format | Online Article Text |
id | pubmed-9239234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92392342022-06-29 S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC Yagmurov, Eldar Gilep, Konstantin Serebryakova, Marina Wolf, Yuri I. Dubiley, Svetlana Severinov, Konstantin mBio Research Article Microcin C (McC)-like compounds are natural Trojan horse peptide-nucleotide antibiotics produced by diverse bacteria. The ribosomally synthesized peptide parts of these antibiotics are responsible for their facilitated transport into susceptible cells. Once inside the cell, the peptide part is degraded, releasing the toxic payload, an isoaspartyl-nucleotide that inhibits aspartyl-tRNA synthetase, an enzyme essential for protein synthesis. Bacteria that produce microcin C-like compounds have evolved multiple ways to avoid self-intoxication. Here, we describe a new strategy through the action of S51 family peptidases, which we name MccG. MccG cleaves the toxic isoaspartyl-nucleotide, rendering it inactive. While some MccG homologs are encoded by gene clusters responsible for biosynthesis of McC-like compounds, most are encoded by standalone genes whose products may provide a basal level of resistance to peptide-nucleotide antibiotics in phylogenetically distant bacteria. American Society for Microbiology 2022-04-25 /pmc/articles/PMC9239234/ /pubmed/35467414 http://dx.doi.org/10.1128/mbio.00805-22 Text en Copyright © 2022 Yagmurov et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Yagmurov, Eldar Gilep, Konstantin Serebryakova, Marina Wolf, Yuri I. Dubiley, Svetlana Severinov, Konstantin S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC |
title | S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC |
title_full | S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC |
title_fullStr | S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC |
title_full_unstemmed | S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC |
title_short | S51 Family Peptidases Provide Resistance to Peptidyl-Nucleotide Antibiotic McC |
title_sort | s51 family peptidases provide resistance to peptidyl-nucleotide antibiotic mcc |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9239234/ https://www.ncbi.nlm.nih.gov/pubmed/35467414 http://dx.doi.org/10.1128/mbio.00805-22 |
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