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Cloning and sequencing of sarA of Staphylococcus aureus, a gene required for the expression of agr

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Cheung, A L, Projan, S J·1994·Journal of Bacteriology

Abstract

To evaluate the effect of a sar mutation on the agr locus, Northern (RNA) blotting was performed to determine the levels of RNAIII, the agr regulatory molecule, in two isogenic pairs of Staphylococcus aureus strains. Our results demonstrated that RNAIII was either significantly diminished or absent in both sar mutants compared with the parents. The RNAIII level was partially restored in sar mutants complemented with an intact sar gene (designated sarA). Additionally, we were able to complement selected sar phenotypes with a plasmid carrying RNAIII (pRN6735). These studies suggest that the sarA gene is necessary for the optimal expression of agr. The sarA gene of strain RN450 was subsequently cloned and sequenced. Sequence analysis revealed an open reading frame of 372 bp with a predicted molecular size of 14,718 Da and a deduced pI of 8.52. The deduced protein sequence has a predominance of charged residues (33%) and shares sequence similarity with the virF gene of Shigella flexneri.

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Metadata

Authors
Cheung, A. L., & Projan, S. J.
Venue
Journal of Bacteriology
Published
1994-07
Volume
176
Issue
13
Pages
4168-4172
ISSN
  • 0021-9193 (ISSN-L)
  • 1098-5530
OpenAlex
W1562798956
Cited by
200
References
0
FWCI
7.19
Type
journal article
Language
en
Open access
green

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Cheung, A. L., & Projan, S. J. (1994). Cloning and sequencing of sarA of Staphylococcus aureus, a gene required for the expression of agr. Journal of Bacteriology. https://doi.org/10.1128/jb.176.13.4168-4172.1994

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.