JAC Advance Access published online on February 25, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkg133
© 2003 by The British Society for Antimicrobial Chemotherapy
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Original article
1 Center for Research in Anti-Infectives & Biotechnology,
Department of Medical Microbiology and Immunology, Creighton University
School of Medicine, Omaha, NE 68178, USA
Received 18 June 2002
; revised 10 August 2002
; accepted 24 December 2002
Serratia marcescens encodes an inducible,
chromosomal
Keywords: ampC, Analyses of ampC gene expression
in Serratia marcescens reveal new regulatory properties
-lactamase, ampC.
Studies addressing the regulation of inducible ampC genes
have focused primarily on Enterobacter cloacae and Citrobacter freundii. The purpose of this study
was to clone and sequence the ampC, ampR and intergenic
region of S. marcescens and examine both inducible
and basal level ampC expression. Sequence analysis
of the S. marcescens ampC gene identified an extended
5' untranslated region (UTR) of 126
nucleotides, which formed a prominent stem-loop structure.
Induction of ampC expression required AmpR, and
the start of transcription was determined using primer extension
analysis. In vivo half-life analysis revealed that
the half-life of the S. marcescens ampC transcript
was 7 min. Confirmation of the in vivo half-life
and the role of the stem-loop structure in the 5' UTR
was demonstrated by comparing transcript half-life and luciferase
expression between a wild-type (WT) and a 5' UTR
stem-loop deletion mutant. These data demonstrated that the
stem-loop structure was involved in transcript stability.
Taken together, these findings indicate that constitutive expression
of S. marcescens ampC is regulated
by both transcriptional initiation and post-transcriptional events.
-lactamase,
Gram-negative bacteria, regulation
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