Generation of tools for expression and purification of the phage-encoded Type I restriction enzyme inhibitor, Ocr.


Journal

Microbiology (Reading, England)
ISSN: 1465-2080
Titre abrégé: Microbiology (Reading)
Pays: England
ID NLM: 9430468

Informations de publication

Date de publication:
Jul 2024
Historique:
medline: 23 7 2024
pubmed: 23 7 2024
entrez: 23 7 2024
Statut: ppublish

Résumé

DNA manipulation is an essential tool in molecular microbiology research that is dependent on the ability of bacteria to take up and preserve foreign DNA by horizontal gene transfer. This process can be significantly impaired by the activity of bacterial restriction modification systems; bacterial operons comprising paired enzymatic activities that protectively methylate host DNA, while cleaving incoming unmodified foreign DNA. Ocr is a phage-encoded protein that inhibits Type I restriction modification systems, the addition of which significantly improves bacterial transformation efficiency. We recently established an improved and highly efficient transformation protocol for the important human pathogen group A

Identifiants

pubmed: 39042422
doi: 10.1099/mic.0.001465
doi:

Substances chimiques

Recombinant Proteins 0
Viral Proteins 0
Deoxyribonucleases, Type I Site-Specific EC 3.1.21.3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Joana Alves (J)

The Roslin Institute, University of Edinburgh, Easter Bush Campus, Midlothian, Scotland, EH25 9RG, UK.

Inga Dry (I)

The Roslin Institute, University of Edinburgh, Easter Bush Campus, Midlothian, Scotland, EH25 9RG, UK.

John H White (JH)

EaStCHEM School of Chemistry, University of Edinburgh, The King's Buildings, Edinburgh, EH9 3FJ, UK.

David T F Dryden (DTF)

Department of Biosciences, University of Durham, South Road, DH1 3LE, UK.

Nicola N Lynskey (NN)

The Roslin Institute, University of Edinburgh, Easter Bush Campus, Midlothian, Scotland, EH25 9RG, UK.

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Classifications MeSH