Journal of Bacteriology, November 1998, p. 6064-6067, Vol. 180, No. 22
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond, Virginia 23298-0678,1 and Department of Molecular and Cell Biology, University of California, Berkeley, California 94720-32042
Received 22 June 1998/Accepted 5 September 1998
The Serratia marcescens extracellular nuclease gene,
nucA, is positively regulated by the product of the
nucC gene. In this study, the upstream region required for
NucC-dependent nuclease expression was defined by using fusions to the
gene encoding chloramphenicol acetyltransferase (cat). This
sequence includes an element of hyphenated dyad symmetry identified
previously as the binding site for the P2 Ogr family of activators.
Footprint analysis confirmed that members of this family of activator
proteins bind to this site, protecting a region between
76 and
59
relative to the start of transcription. The activator binding site in
the nucA promoter lies one turn of the helix upstream from
the corresponding sites in the P2 and P4 late promoters. The effects of
deletions between the downstream end of the activator binding site and
the putative
35 region are consistent with a strict helical phasing requirement for activation.
Present address: Kosan Biosciences, Burlingame, CA 94010.
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