Transcriptome analysis of temporal regulation of carbon metabolism by CcpA in Bacillus subtilis reveals additional target genes

被引:55
作者
Lulko, Andrzej T. [1 ]
Buist, Girbe [1 ]
Kok, Jan [1 ]
Kuipers, Oscar P. [1 ]
机构
[1] Univ Groningen, Mol Genet Grp, Groningen Biomol Sci & Biotechnol Inst, NL-9751 NN Haren, Netherlands
关键词
CcpA; CCR; CCA; cre; DNA microarrays; time series; Bacillus subtilis; man; opu; yhb;
D O I
10.1159/000096463
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The pleiotropic regulator of carbon metabolism in Grampositive bacteria, CcpA, regulates gene expression by binding to so-called cre elements, which are located either upstream or in promoter regions, or in open-reading frames. In this study we compared the transcriptomes of Bacillus subtilis 168 and its ccpA deletion mutant during growth in glucose-containing rich medium. Although growth was similar, glucose was completely consumed by the wild-type strain in the stationary phase, while it was still present in the culture of the mutant. At that stage, direct and indirect effects on gene expression were observed. During exponential growth, CcpA mainly influences the carbohydrate and energy metabolism, whereas from transition phase onwards its function expands on a broader range of physiological processes including nucleotide metabolism, cell motility and protein synthesis. A genome wide search revealed new putative cre sites, which could function in vivo according to our transcriptome data. Comparison of our data with published transcriptome data of ccpA mutant analysis in the exponential growth phase confirmed earlier identified CcpA regulon members. It also allowed identification of potential new CcpA-repressed genes, amongst others ycgN and the ydh operon. Novel activated members include opuE and the opuAABC, yhb and man operons, which all have a putative cre site that appears to be dependent on helical topology. A comparative analysis of these genes with the known activated genes i.e. ackA and pta revealed the presence of a possible upstream activating region (UAR) as has been shown to be functional for the activation of ackA. The data suggest that at later growth phases CcpA may regulate gene expression by itself or complexed with other, yet unknown cofactors. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:82 / 95
页数:14
相关论文
共 57 条
[31]   Evaluation and characterization of catabolite-responsive elements (cre) of Bacillus subtilis [J].
Miwa, Y ;
Nakata, A ;
Ogiwara, A ;
Yamamoto, M ;
Fujita, Y .
NUCLEIC ACIDS RESEARCH, 2000, 28 (05) :1206-1210
[32]   Transcriptional activation of the Bacillus subtilis ackA promoter requires sequences upstream of the CcpA binding site [J].
Moir-Blais, TR ;
Grundy, FJ ;
Henkin, TM .
JOURNAL OF BACTERIOLOGY, 2001, 183 (07) :2389-2393
[33]   Catabolite repression mediated by the CcpA protein in Bacillus subtilis:: novel modes of regulation revealed by whole-genome analyses [J].
Moreno, MS ;
Schneider, BL ;
Maile, RR ;
Weyler, W ;
Saier, MH .
MOLECULAR MICROBIOLOGY, 2001, 39 (05) :1366-1381
[34]   Catabolite regulation of the pta gene as part of carbon flow pathways in Bacillus subtilis [J].
Presecan-Siedel, E ;
Galinier, A ;
Longin, R ;
Deutscher, J ;
Danchin, A ;
Glaser, P ;
Martin-Verstraete, I .
JOURNAL OF BACTERIOLOGY, 1999, 181 (22) :6889-6897
[35]   Novel phosphotransferase system genes revealed by genome analysis -: the complete complement of PTS proteins encoded within the genome of Bacillus subtilis [J].
Reizer, J ;
Bachem, S ;
Reizer, A ;
Arnaud, M ;
Saier, MH ;
Stülke, J .
MICROBIOLOGY-UK, 1999, 145 :3419-3429
[36]   OligoArray 2.0: design of oligonucleotide probes for DNA microarrays using a thermodynamic approach [J].
Rouillard, JM ;
Zuker, M ;
Gulari, E .
NUCLEIC ACIDS RESEARCH, 2003, 31 (12) :3057-3062
[37]   Sequence and genetic organization of a Bacillus subtilis operon encoding 2,3-dihydroxybenzoate biosynthetic enzymes [J].
Rowland, BM ;
Grossman, TH ;
Osburne, MS ;
Taber, HW .
GENE, 1996, 178 (1-2) :119-123
[38]   Maltose and maltodextrin utilization by Bacillus subtilis [J].
Schönert, S ;
Seitz, S ;
Krafft, H ;
Feuerbaum, EA ;
Andernach, I ;
Witz, G ;
Dahl, MK .
JOURNAL OF BACTERIOLOGY, 2006, 188 (11) :3911-3922
[39]   Structural basis for allosteric control of the transcription regulator CcpA by the phosphoprotein HPr-Ser46-P [J].
Schumacher, MA ;
Allen, GS ;
Diel, M ;
Seidel, G ;
Hillen, W ;
Brennan, RG .
CELL, 2004, 118 (06) :731-741
[40]   Quantitative interdependence of coeffectors, CcpA and cre in carbon catabolite regulation of Bacillus subtilis [J].
Seidel, G ;
Diel, M ;
Fuchsbauer, N ;
Hillen, W .
FEBS JOURNAL, 2005, 272 (10) :2566-2577