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Journal of Bacteriology, January 2000, p. 146-154, Vol. 182, No. 1
R&D, Valio Ltd., FIN-00039 Valio,
Helsinki,1 Agricultural Research Centre of
Finland, Food Research Institute, FIN-31600
Jokioinen,3 and Department of Applied
Chemistry and Microbiology, University of Helsinki, FIN-00014
University of Helsinki,4 Finland, and
Department of Dairy and Food Science, The Royal Veterinary
and Agricultural University, DK-1958 Frederiksberg C,
Denmark2
Received 15 July 1999/Accepted 29 September 1999
A peptidase gene expressing X-prolyl dipeptidyl aminopeptidase
(PepX) activity was cloned from Lactobacillus rhamnosus 1/6 by using the chromogenic substrate
L-glycyl-L-prolyl-
0021-9193/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
X-Prolyl Dipeptidyl Aminopeptidase Gene
(pepX) Is Part of the glnRA Operon in
Lactobacillus rhamnosus

and
-naphthylamide for
screening of a genomic library in Escherichia coli. The
nucleotide sequence of a 3.5-kb HindIII fragment expressing
the peptidase activity revealed one complete open reading frame (ORF)
of 2,391 nucleotides. The 797-amino-acid protein encoded by this ORF
was shown to be 40, 39, and 36% identical with PepXs from
Lactobacillus helveticus, Lactobacillus
delbrueckii, and Lactococcus lactis, respectively. By
Northern analysis with a pepX-specific probe, transcripts
of 4.5 and 7.0 kb were detected, indicating that pepX is
part of a polycistronic operon in L. rhamnosus. Cloning and sequencing of the upstream region of pepX revealed the
presence of two ORFs of 360 and 1,338 bp that were shown to be able to encode proteins with high homology to GlnR and GlnA proteins, respectively. By multiple primer extension analyses, the only functional promoter in the pepX region was located 25 nucleotides upstream of glnR. Northern analysis with
glnA- and pepX-specific probes indicated that
transcription from glnR promoter results in a 2.0-kb
dicistronic glnR-glnA transcript and also in a longer read-through polycistronic transcript of 7.0 kb that was detected with
both probes in samples from cells in exponential growth phase. The
glnA gene was disrupted by a single-crossover recombinant event using a nonreplicative plasmid carrying an internal part of
glnA. In the disruption mutant, glnRA-specific
transcription was derepressed 10-fold compared to the wild type, but
the 7.0-kb transcript was no longer detectable with either the
glnA- or pepX-specific probe, demonstrating
that pepX is indeed part of glnRA operon in
L. rhamnosus. Reverse transcription-PCR analysis further
supported this operon structure. An extended stem-loop structure was
identified immediately upstream of pepX in the
glnA-pepX intergenic region, a sequence that showed
homology to a 23S-5S intergenic spacer and to several other L. rhamnosus-related entries in data banks.
*
Corresponding author. Mailing address: Department of
Dairy and Food Science, The Royal Veterinary and Agricultural
University, Rolighedsvej 30, DK-1958 Frederiksberg C, Denmark.
Phone: 45 35 28 32 56. Fax: 45 35 28 32 31. E-mail:
pekka{at}biobase.dk.
Present address: Faculty of Veterinary Medicine, University of
Helsinki, FIN-00014 University of Helsinki, Finland.
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