NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE23499 Query DataSets for GSE23499
Status Public on Jul 25, 2012
Title The IHF regulon of exponentially growing Pseudomonas putida cells
Platform organism Pseudomonas putida KT2440
Sample organism Pseudomonas putida
Experiment type Expression profiling by array
Summary Integration host factor (IHF) sites are largely absent from intergenic regions of ORFs encoding central metabolic functions in Pseudomonas putida mt-2. To gain an insight into this unequal distribution of otherwise abundant IHF-binding sequences, the transcriptome of IHF-plus and IHF-minus cells growing exponentially on glucose as sole carbon source was examined. In parallel, the cognate metabolic fluxes of the wild-type P. putida strain and its ihfA derivative were determined by culturing cells to a steady-state physiological regime with (13) C-labelled glucose. While expression of many transcripts was altered by the lack of IHF, flux balance analysis revealed that the ihfA mutation did not influence central carbon metabolism. Identification of multiple IHF sites adjacent to genes responsive to the factor allowed a refinement of the consensus and the mapping of the preferred binding positions for activation or repression of associated promoters. That few (if any) of the genes affected by IHF involved core pathways suggested that the central carbon metabolism tolerates the loss of the factor. Instead, IHF controlled various cell surface-related functions and downregulated genes encoding ribosomal proteins, the alpha subunit of RNA polymerase and components of the ATP synthase. These results were confirmed with lacZ fusions to a suite of promoters detected in the transcriptome as affected by IHF. Taken together, the data suggest that IHF plays a role in the physiological shift that sets P. putida for entering stationary phase.
 
Overall design We compared the transcriptional profiles of P. putida mt-2 and the ihfA mutant. Samples were hybridized on a P. putida genome-wide oligonucleotide-based DNA microarray (Progenika Biopharma SA). RNA samples of seven independent biological samples were mixed in three pools. A dye-swap was performed.
 
Contributor(s) Silva-Rocha R, Chavarría M, Kleijn RJ, Sauer U, de Lorenzo V
Citation(s) 22510163
Submission date Aug 06, 2010
Last update date Sep 21, 2012
Contact name Victor de Lorenzo
Organization name CNB-CSIC
Department Systems Biology
Street address Darwin 3
City Campus de Cantoblanco
State/province Madrid
ZIP/Postal code 28049
Country Spain
 
Platforms (1)
GPL10767 Progenika Biopharma Pseudomonas putida MPA-02-0001
Samples (3)
GSM575620 mt-2 vs IHF-, rep1
GSM575621 mt-2 vs IHF-, rep2
GSM575622 mt-2 vs IHF-, rep3
Relations
BioProject PRJNA131011

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE23499_RAW.tar 3.7 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap