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Antimicrobial Peptide Resistance of Vibrio cholerae Results from an LPS Modification Pathway Related to Nonribosomal Peptide Synthetases
[Image: see text] The current pandemic El Tor biotype of O1 Vibrio cholerae is resistant to polymyxins, whereas the previous pandemic strain of the classical biotype is polymyxin sensitive. The almEFG operon found in El Tor V. cholerae confers >100-fold resistance to polymyxins through the glycyl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520716/ https://www.ncbi.nlm.nih.gov/pubmed/25068415 http://dx.doi.org/10.1021/cb500438x |
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author | Henderson, Jeremy C. Fage, Christopher D. Cannon, Joe R. Brodbelt, Jennifer S. Keatinge-Clay, Adrian T. Trent, M. Stephen |
author_facet | Henderson, Jeremy C. Fage, Christopher D. Cannon, Joe R. Brodbelt, Jennifer S. Keatinge-Clay, Adrian T. Trent, M. Stephen |
author_sort | Henderson, Jeremy C. |
collection | PubMed |
description | [Image: see text] The current pandemic El Tor biotype of O1 Vibrio cholerae is resistant to polymyxins, whereas the previous pandemic strain of the classical biotype is polymyxin sensitive. The almEFG operon found in El Tor V. cholerae confers >100-fold resistance to polymyxins through the glycylation of lipopolysaccharide. Here, we present the mechanistic determination of initial steps in the AlmEFG pathway. We verify that AlmF is an aminoacyl carrier protein and identify AlmE as the enzyme required to activate AlmF as a functional carrier protein. A combination of structural information and activity assays was used to identify a pair of active site residues that are important for mediating AlmE glycine specificity. Overall, the structure of AlmE in complex with its glycyl-adenylate intermediate reveals that AlmE is related to Gram-positive d-alanine/d-alanyl carrier protein ligase, while the trio of proteins in the AlmEFG system forms a chemical pathway that resembles the division of labor in nonribosomal peptide synthetases. |
format | Online Article Text |
id | pubmed-4520716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45207162015-08-01 Antimicrobial Peptide Resistance of Vibrio cholerae Results from an LPS Modification Pathway Related to Nonribosomal Peptide Synthetases Henderson, Jeremy C. Fage, Christopher D. Cannon, Joe R. Brodbelt, Jennifer S. Keatinge-Clay, Adrian T. Trent, M. Stephen ACS Chem Biol [Image: see text] The current pandemic El Tor biotype of O1 Vibrio cholerae is resistant to polymyxins, whereas the previous pandemic strain of the classical biotype is polymyxin sensitive. The almEFG operon found in El Tor V. cholerae confers >100-fold resistance to polymyxins through the glycylation of lipopolysaccharide. Here, we present the mechanistic determination of initial steps in the AlmEFG pathway. We verify that AlmF is an aminoacyl carrier protein and identify AlmE as the enzyme required to activate AlmF as a functional carrier protein. A combination of structural information and activity assays was used to identify a pair of active site residues that are important for mediating AlmE glycine specificity. Overall, the structure of AlmE in complex with its glycyl-adenylate intermediate reveals that AlmE is related to Gram-positive d-alanine/d-alanyl carrier protein ligase, while the trio of proteins in the AlmEFG system forms a chemical pathway that resembles the division of labor in nonribosomal peptide synthetases. American Chemical Society 2014-07-28 2014-10-17 /pmc/articles/PMC4520716/ /pubmed/25068415 http://dx.doi.org/10.1021/cb500438x Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Henderson, Jeremy C. Fage, Christopher D. Cannon, Joe R. Brodbelt, Jennifer S. Keatinge-Clay, Adrian T. Trent, M. Stephen Antimicrobial Peptide Resistance of Vibrio cholerae Results from an LPS Modification Pathway Related to Nonribosomal Peptide Synthetases |
title | Antimicrobial Peptide Resistance of Vibrio
cholerae Results from an LPS Modification Pathway Related
to Nonribosomal Peptide Synthetases |
title_full | Antimicrobial Peptide Resistance of Vibrio
cholerae Results from an LPS Modification Pathway Related
to Nonribosomal Peptide Synthetases |
title_fullStr | Antimicrobial Peptide Resistance of Vibrio
cholerae Results from an LPS Modification Pathway Related
to Nonribosomal Peptide Synthetases |
title_full_unstemmed | Antimicrobial Peptide Resistance of Vibrio
cholerae Results from an LPS Modification Pathway Related
to Nonribosomal Peptide Synthetases |
title_short | Antimicrobial Peptide Resistance of Vibrio
cholerae Results from an LPS Modification Pathway Related
to Nonribosomal Peptide Synthetases |
title_sort | antimicrobial peptide resistance of vibrio
cholerae results from an lps modification pathway related
to nonribosomal peptide synthetases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520716/ https://www.ncbi.nlm.nih.gov/pubmed/25068415 http://dx.doi.org/10.1021/cb500438x |
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