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Journal of Bacteriology, September 1998, p. 4746-4749, Vol. 180, No. 17
Department of Veterinary Pathobiology,
University of Illinois, Urbana, Illinois 61801
Received 5 March 1998/Accepted 12 June 1998
An Escherichia coli DNA fragment was identified that
contained part of the
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
In Vivo Expression of the
-Glucoside
(bgl) Operon of Escherichia coli Occurs in
Mouse Liver
-glucoside (bgl) operon. This
fragment was identified because it contained a promoter that was
responsible for the expression of a reporter gene, the chloramphenicol
acetyltransferase gene, in a mouse liver during bacterial infection but
not when a bacterial clone was grown in vitro. This fragment contained
a promoter and a rho-independent transcription terminator which were
flanked by the 3' end of bglG and the 5' end of
bglF. Reverse transcription-PCR confirmed that
cat-specific mRNA was produced in infected mouse liver but
not in vitro. mRNA encoding the positive regulator of the
bgl operon, bglG, also was detected in mouse
liver infected with an E. coli strain. These results
demonstrated that expression of the bgl operon occurs in
infected mouse liver and suggests a unique role for this operon in
vivo.
*
Corresponding author. Mailing address: Department of
Veterinary Pathobiology, University of Illinois, 2001 S. Lincoln Ave., Urbana, IL 61801. Phone: (217) 244-7999. Fax: (217) 244-7421. E-mail:
m-khan{at}staff.uiuc.edu.
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