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Cloning, characterization, and sequencing of an accessory gene regulator (agr) in Staphylococcus aureus

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Peng, H L, Novick, R P, Kreiswirth, B, Kornblum, J, Schlievert, P·1988·Journal of Bacteriology

Abstract

We have previously identified a gene in Staphylococcus aureus, agr, whose activity is required for high-level post-exponential-phase expression of a series of secreted proteins. In this paper, we describe the cloning of this gene in Escherichia coli by using an inserted transposon (Tn551) as a cloning probe. The cloned gene, consisting of a 241-codon open reading frame containing the site of the transposon insertion, was recloned to an S. aureus vector, pSK265, and shown to be functional in S. aureus. Activity was evaluated by determinations of alpha-hemolysin, beta-hemolysin, and toxic shock syndrome toxin-1 production in early-stationary-phase cultures. The cloned gene showed considerable variation with respect to different exoproteins and different host strains compared with the chromosomal agr determinant; this variation could not be attributed to the higher copy number of the cloned gene and probably reflects inapparent subtleties of the regulatory system.

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Metadata

Authors
Peng, H. L., Novick, R. P., Kreiswirth, B., Kornblum, J., & Schlievert, P.
Venue
Journal of Bacteriology
Published
1988-09
Volume
170
Issue
9
Pages
4365-4372
ISSN
  • 0021-9193 (ISSN-L)
  • 1098-5530
OpenAlex
W1790927204
Cited by
566
References
0
FWCI
11.14
Type
journal article
Language
en
Open access
green

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Peng, H. L., Novick, R. P., Kreiswirth, B., Kornblum, J., & Schlievert, P. (1988). Cloning, characterization, and sequencing of an accessory gene regulator (agr) in Staphylococcus aureus. Journal of Bacteriology. https://doi.org/10.1128/jb.170.9.4365-4372.1988

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