Affiliation:
1. Departamento de Biotecnologı́a, Instituto de Agroquı́mica y Tecnologı́a de Alimentos (CSIC), 46100 Burjassot, Valencia, Spain,1and
2. Laboratoire de Recherches sur la Viande, INRA-Jouy, Domaine de Vilvert, 78352 Jouy en Josas, France2
Abstract
ABSTRACT
Lactobacillus sake
can use arginine via the arginine deiminase (ADI) pathway. We designed degenerate primers based on an alignment of known sequences of ornithine transcarbamoylase (OTC)-encoding genes in order to amplify the
L. sake
counterpart sequences by PCR. Screening a genomic library of
L. sake
in λEMBL3 allowed us to isolate a clone containing a 10-kb
L. sake
genomic DNA insert. Sequence analysis revealed that the genes involved in arginine catabolism were clustered and encoded ADI (
arcA
), OTC (
arcB
), carbamate kinase (
arcC
), and a putative carrier with high similarity to the arginine/ornithine antiporter of
Pseudomonas aeruginosa
(
arcD
). Additionally, a putative transaminase-encoding gene (
arcT
) was located in this region. The genes followed the order
arcA arcB arcC arcT arcD
, which differs from that found in other microorganisms.
arcA
,
arcB
,
arcC
, and
arcD
mutants were constructed, and the ADI pathway was impaired in all of them. Transcriptional studies indicated that
arcA
gene is subject to catabolite repression, and under the conditions used, several transcripts could be detected, suggesting the existence of different initiation sites or processing of a larger mRNA.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
104 articles.
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