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Characterization of the Neisseria meningitidis Helicase RecG.
Beyene, Getachew Tesfaye; Balasingham, Seetha V; Frye, Stephan A; Namouchi, Amine; Homberset, Håvard; Kalayou, Shewit; Riaz, Tahira; Tønjum, Tone.
Afiliación
  • Beyene GT; Department of Microbiology, University of Oslo, Oslo, Norway.
  • Balasingham SV; Department of Microbiology, Oslo University Hospital (Rikshospitalet), Oslo, Norway.
  • Frye SA; Department of Microbiology, Oslo University Hospital (Rikshospitalet), Oslo, Norway.
  • Namouchi A; Department of Microbiology, Oslo University Hospital (Rikshospitalet), Oslo, Norway.
  • Homberset H; Department of Microbiology, University of Oslo, Oslo, Norway.
  • Kalayou S; Department of Microbiology, University of Oslo, Oslo, Norway.
  • Riaz T; Department of Microbiology, University of Oslo, Oslo, Norway.
  • Tønjum T; Department of Microbiology, University of Oslo, Oslo, Norway.
PLoS One ; 11(10): e0164588, 2016.
Article en En | MEDLINE | ID: mdl-27736945
Neisseria meningitidis (Nm) is a Gram-negative oral commensal that opportunistically can cause septicaemia and/or meningitis. Here, we overexpressed, purified and characterized the Nm DNA repair/recombination helicase RecG (RecGNm) and examined its role during genotoxic stress. RecGNm possessed ATP-dependent DNA binding and unwinding activities in vitro on a variety of DNA model substrates including a Holliday junction (HJ). Database searching of the Nm genomes identified 49 single nucleotide polymorphisms (SNPs) in the recGNm including 37 non-synonymous SNPs (nsSNPs), and 7 of the nsSNPs were located in the codons for conserved active site residues of RecGNm. A transient reduction in transformation of DNA was observed in the Nm ΔrecG strain as compared to the wildtype. The gene encoding recGNm also contained an unusually high number of the DNA uptake sequence (DUS) that facilitate transformation in neisserial species. The differentially abundant protein profiles of the Nm wildtype and ΔrecG strains suggest that expression of RecGNm might be linked to expression of other proteins involved in DNA repair, recombination and replication, pilus biogenesis, glycan biosynthesis and ribosomal activity. This might explain the growth defect that was observed in the Nm ΔrecG null mutant.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Bacteriano / Clonación Molecular / ADN Helicasas / Neisseria meningitidis Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Bacteriano / Clonación Molecular / ADN Helicasas / Neisseria meningitidis Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Estados Unidos