Affiliation:
1. Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET) and Departamento de Microbiología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Rosario, Argentina
Abstract
ABSTRACT
Although
Lactococcus
is one of the most extensively studied lactic acid bacteria and is the paradigm for biochemical studies of citrate metabolism, little information is available on the regulation of the citrate lyase complex. In order to fill this gap, we characterized the genes encoding the subunits of the citrate lyase of
Lactococcus lactis
CRL264, which are located on an 11.4-kb chromosomal DNA region. Nucleotide sequence analysis revealed a cluster of eight genes in a new type of genetic organization. The
citM-citCDEFXG
operon (
cit
operon) is transcribed as a single polycistronic mRNA of 8.6 kb. This operon carries a gene encoding a malic enzyme (CitM, a putative oxaloacetate decarboxylase), the structural genes coding for the citrate lyase subunits (
citD
,
citE
, and
citF
), and the accessory genes required for the synthesis of an active citrate lyase complex (
citC
,
citX
, and
citG
). We have found that the
cit
operon is induced by natural acidification of the medium during cell growth or by a shift to media buffered at acidic pHs. Between the
citM
and
citC
genes is a divergent open reading frame whose expression was also increased at acidic pH, which was designated
citI
. This inducible response to acid stress takes place at the transcriptional level and correlates with increased activity of citrate lyase. It is suggested that coordinated induction of the citrate transporter, CitP, and citrate lyase by acid stress provides a mechanism to make the cells (more) resistant to the inhibitory effects of the fermentation product (lactate) that accumulates under these conditions.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
60 articles.
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