Affiliation:
1. Department of Molecular Genetics, University of Groningen, Groningen Biomolecular Sciences and Biotechnology Institute, PO Box 14, 9750 AA Haren, The Netherlands
Abstract
ABSTRACT
Carbon catabolite control protein A (CcpA) is the main regulator involved in carbon catabolite repression in gram-positive bacteria. Time series gene expression analyses of
Lactococcus lactis
MG1363 and
L. lactis
MG1363Δ
ccpA
using DNA microarrays were used to define the CcpA regulon of
L. lactis
. Based on a comparison of the transcriptome data with putative CcpA binding motifs (
cre
sites) in promoter sequences in the genome of
L. lactis
, 82 direct targets of CcpA were predicted. The main differences in time-dependent expression of CcpA-regulated genes were differences between the exponential and transition growth phases. Large effects were observed for carbon and nitrogen metabolic genes in the exponential growth phase. Effects on nucleotide metabolism genes were observed primarily in the transition phase. Analysis of the positions of putative
cre
sites revealed that there is a link between either repression or activation and the location of the
cre
site within the promoter region. Activation was observed when putative
cre
sites were located upstream of the hexameric −35 sequence at an average position of −56.5 or further upstream with decrements of 10.5 bp. Repression was observed when the
cre
site was located in or downstream of putative −35 and −10 sequences. The highest level of repression was observed when the
cre
site was present at a defined side of the DNA helix relative to the canonical −10 sequence. Gel retardation experiments, Northern blotting, and enzyme assays showed that CcpA represses its own expression and activates the expression of the divergently oriented prolidase-encoding
pepQ
gene, which constitutes a link between regulation of carbon metabolism and regulation of nitrogen metabolism.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
135 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献