Structural and Functional Analysis of the Gene Cluster Encoding the Enzymes of the Arginine Deiminase Pathway of Lactobacillus sake

Author:

Zúñiga Manuel1,Champomier-Verges Marie2,Zagorec Monique2,Pérez-Martínez Gaspar1

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

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