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Journal of Bacteriology, September 2000, p. 4822-4828, Vol. 182, No. 17
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Analysis of Genetic Elements Controlling
Staphylococcus aureus lrgAB Expression: Potential Role of
DNA Topology in SarA Regulation
David F.
Fujimoto,
Eric W.
Brunskill,
and
Kenneth W.
Bayles*
Department of Microbiology, Molecular Biology
and Biochemistry, University of Idaho, Moscow, Idaho 83844-3052
Received 29 March 2000/Accepted 16 June 2000
Penicillin-induced killing and murein hydrolase activity in
Staphylococcus aureus are dependent on a variety of
regulatory elements, including the LytSR two-component regulatory
system and the virulence factor regulators Agr and Sar. The LytSR
effects on these processes can be explained, in part, by the recent
finding that a LytSR-regulated operon, designated lrgAB,
affects murein hydrolase activity and penicillin tolerance. To
examine the regulation of lrgAB expression in greater
detail, we performed Northern blot and promoter fusion analyses. Both
methods revealed that Agr and Sar, like LytSR, positively regulate
lrgAB expression. A mutation in the agr locus
reduced lrgAB expression approximately sixfold, while the
sar mutation reduced lrgAB expression to
undetectable levels. cis-acting regulatory elements
involved in lrgAB expression were identified by fusing
various fragments of the lrgAB promoter region to the
xylE reporter gene and integrating these constructs into
the chromosome. Catechol 2,3-dioxygenase assays identified DNA
sequences, including an inverted repeat and intrinsic bend sites, that
contribute to maximal lrgAB expression. Confirmation of the
importance of the inverted repeat was achieved by demonstrating that multiple copies of the inverted repeat reduced lrgAB
promoter activity, presumably by titrating out a positive regulatory
factor. The results of this study demonstrate that lrgAB
expression responds to a variety of positive regulatory factors and
suggest that specific DNA topology requirements are important for
optimal expression.
*
Corresponding author. Mailing address: Department of
Microbiology, Molecular Biology and Biochemistry, College of
Agriculture, University of Idaho, Moscow, ID 83844-3052. Phone: (208)
885-7164. Fax: (208) 885-6518. E-mail: kbayles{at}uidaho.edu.

Present address: The Childrens' Hospital Research Foundation,
Division of Developmental Biology, Cincinnati, OH
45229.
Journal of Bacteriology, September 2000, p. 4822-4828, Vol. 182, No. 17
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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