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Staphylococcus aureus endoribonuclease III purification and properties

Authors :
Chevalier, Clément
Huntzinger, Eric
Fechter, Pierre
Boisset, Sandrine
Vandenesch, François
Romby, Pascale
Geissmann, Thomas
Architecture et Réactivité de l'ARN (ARN)
Institut de biologie moléculaire et cellulaire (IBMC)
Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)
Immunité infection vaccination (I2V)
Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-IFR128-Institut National de la Santé et de la Recherche Médicale (INSERM)
Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR128-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon
Source :
Methods in Enzymology, Methods in Enzymology, Elsevier, 2008, 447, pp.309-27. ⟨10.1016/S0076-6879(08)02216-7⟩
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

International audience; Staphylococcus aureus ribonuclease III (Sa-RNase III) belongs to the enzyme family known to process double-stranded RNAs consisting of two turns of the RNA helix. Although the enzyme is thought to play a role in ribosomal RNA processing and gene regulation, the deletion of the rnc gene in S. aureus does not affect cell growth in rich medium. S. aureus RNase III acts in concert with regulatory RNAIII to repress the expression of several mRNAs encoding virulence factors. The action of the RNase is most likely to initiate the degradation of repressed mRNAs leading to an irreversible repression. In this chapter, we describe the overexpression and purification of recombinant RNase III from S. aureus, and we show that its biochemical properties are similar to the orthologous enzyme from Escherichia coli. Both enzymes similarly recognize and cleave different RNA substrates and RNA-mRNA duplexes.

Details

Language :
English
ISSN :
00766879
Database :
OpenAIRE
Journal :
Methods in Enzymology, Methods in Enzymology, Elsevier, 2008, 447, pp.309-27. ⟨10.1016/S0076-6879(08)02216-7⟩
Accession number :
edsair.pmid.dedup....6aed9b35697b02a7012f67ca6686a955
Full Text :
https://doi.org/10.1016/S0076-6879(08)02216-7⟩