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J Bacteriol, February 1998, p. 840-845, Vol. 180, No. 4
Department of Biochemistry and Microbiology,
University of Victoria, Victoria, British Columbia V8W
3P6,1 and
Microtek International
Ltd., Saanichton, British Columbia V8X 3X1,2
Canada
Received 21 August 1997/Accepted 16 December 1997
A Tn10 insertion affecting SEF14 fimbrial synthesis in
Salmonella enteritidis was located 13 bp upstream of a gene
designated fimU. The 77-bp DNA sequence of fimU
from S. enteritidis was identical to that of
fimU encoding tRNAArg (UCU) from
Salmonella typhimurium and 96% identical to that of the
Escherichia coli argU homolog. Furthermore, the open
reading frame adjacent to and overlapping the 3' end of
fimU was similar to the prophage DLP12 integrase gene. The
fimU-encoded transcript comigrated with total cellular tRNA
and was predicted to form a tRNA-like cloverleaf structure containing
the arginine anticodon UCU. Thus, fimU encoded a
tRNAArg specific for the rare codon AGA. fimU
mapped to the SEF21 fim operon located 15 C's from the
sef14 gene cluster. Although fimU was located
within the SEF21 fim gene cluster, the fimU
Tn10 insertion mutant of S. enteritidis was
found to be defective in SEF14 as well as SEF21 (type 1) fimbria
production. SEF17 and SEF18 fimbria production was not affected.
Complementation of this mutant with plasmid-borne fimU
restored normal production of the fimbrins SefA and FimA as well as
their respective fimbriae SEF14 and SEF21. This is the first
description of tRNA simultaneously controlling the production of two
distinct fimbriae.
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
tRNAArg (fimU) and
Expression of SEF14 and SEF21 in Salmonella
enteritidis
*
Corresponding author. Mailing address: Department of
Biochemistry and Microbiology, University of Victoria, Victoria, B.C. V8W 3P6, Canada. Phone: (250) 721 7078. Fax: (250) 721 8882. E-mail: wkay{at}uvic.ca.
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