Characterization of permissive and non-permissive peptide insertion sites in chloramphenicol acetyltransferase.


Journal

Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 20 04 2020
revised: 02 06 2020
accepted: 10 07 2020
pubmed: 21 7 2020
medline: 22 6 2021
entrez: 21 7 2020
Statut: ppublish

Résumé

The growing prevalence of antibiotic resistance in numerous pathogenic bacteria is a major public health concern and urgently requires the development of new therapeutic approaches. Multidrug resistant species that remain sensitive to chloramphenicol (CAM) treatment have engendered renewed interest in using this drug as a modern day antimicrobial agent. High-level resistance to CAM commonly is mediated by chloramphenicol acetyltransferase (CAT) which catalyzes the acetylation of CAM and renders the drug inactive. Of the three main types (CAT

Identifiants

pubmed: 32687937
pii: S0882-4010(20)30761-0
doi: 10.1016/j.micpath.2020.104395
pii:
doi:

Substances chimiques

Peptides 0
Chloramphenicol 66974FR9Q1
Chloramphenicol O-Acetyltransferase EC 2.3.1.28

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104395

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Andrew Goodale (A)

Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, UK.

Fanourios Michailidis (F)

Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, UK.

Rachel Watts (R)

Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, UK.

Shi Chen Chok (SC)

Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, UK.

Finbarr Hayes (F)

Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, M13 9PL, UK. Electronic address: finbarr.hayes@manchester.ac.uk.

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Classifications MeSH