The IHF regulon of exponentially growing Pseudomonas putida cells

• Published in: Environmental microbiology 2013-01, Vol.15 (1), p.49-63
• Main Authors: Silva-Rocha, Rafael, Chavarría, Max, Kleijn, Roelco J., Sauer, Uwe, de Lorenzo, Víctor
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - biosynthesis; Animal, plant and microbial ecology; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Bacteriology; Biofilms; Biological and medical sciences; Carbon Isotopes - analysis; Enzymes; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation, Bacterial; General aspects; Integration Host Factors - genetics; Integration Host Factors - metabolism; Microbial ecology; Microbiology; Miscellaneous; Pseudomonas putida; Pseudomonas putida - genetics; Pseudomonas putida - growth & development; Pseudomonas putida - metabolism; Regulon - genetics; RNA polymerase; Transcriptome
• ISSN: 1462-2912; 1462-2920
• DOI: 10.1111/j.1462-2920.2012.02750.x

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 13C‐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.