Journal of Bacteriology, March 2005, p. 2148-2156, Vol. 187, No. 6
0021-9193/05/$08.00+0 doi:10.1128/JB.187.6.2148-2156.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Transcriptome Analysis of the Rhodobacter sphaeroides PpsR Regulon: PpsR as a Master Regulator of Photosystem Development
Oleg V. Moskvin,
Larissa Gomelsky, and
Mark Gomelsky*
Department of Molecular Biology, University of Wyoming, Laramie, Wyoming
Received 13 August 2004/
Accepted 8 December 2004
PpsR from the anoxygenic phototrophic bacterium Rhodobacter sphaeroides has been known as an oxygen- and light-dependent repressor of bacteriochlorophyll and carotenoid biosynthesis genes and puc operons involved in photosystem development. However, the putative PpsR-binding sites, TGTN12ACA, are also located upstream of numerous nonphotosystem genes, thus raising the possibility that the role of PpsR is broader. To characterize the PpsR regulon, transcriptome profiling was performed on the wild-type strain grown at high and low oxygen tensions, on the strain overproducing PpsR, and on the ppsR mutant. Transcriptome analysis showed that PpsR primarily regulates photosystem genes; the consensus PpsR binding sequence is TGTcN10gACA (lowercase letters indicate lesser conservation); the presence of two binding sites is required for repression in vivo. These findings explain why numerous single TGTN12ACA sequences are nonfunctional. In addition to photosystem genes, the hemC and hemE genes involved in the early steps of tetrapyrrole biosynthesis were identified as new direct targets of PpsR repression. Unexpectedly, PpsR was found to indirectly repress the puf and puhA operons encoding photosystem core proteins. The upstream regions of these operons contain no PpsR binding sites. Involvement in regulation of these operons suggests that PpsR functions as a master regulator of photosystem development. Upregulation of the puf and puhA operons that resulted from ppsR inactivation was sufficient to restore the ability to grow phototrophically to the prrA mutant. PrrA, the global redox-dependent activator, was previously considered indispensable for phototrophic growth. It is revealed that the PrrBA and AppA-PpsR systems, believed to work independently, in fact interact and coordinately regulate photosystem development.
* Corresponding author. Mailing address: Department of Molecular Biology, University of Wyoming, Dept. 3944, 1000 E. University Ave., Laramie, WY 82071. Phone: (307) 766-3522. Fax: (307) 766-3875. E-mail: gomelsky{at}uwyo.edu.
Supplemental material for this article may be found at http://jb.asm.org/.
Journal of Bacteriology, March 2005, p. 2148-2156, Vol. 187, No. 6
0021-9193/05/$08.00+0 doi:10.1128/JB.187.6.2148-2156.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
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