Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 144 (1998), 267-278; DOI  10.1099/00221287-144-2-267
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pemberton, J. M.
Right arrow Articles by McEwan, A. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pemberton, J. M.
Right arrow Articles by McEwan, A. G.
Agricola
Right arrow Articles by Pemberton, J. M.
Right arrow Articles by McEwan, A. G.

Regulation of photosynthetic gene expression in purple bacteria

John M. Pemberton, Irene M. Horne and Alastair G. McEwan

Department of Microbiology, The University of Queensland, St Lucia 4072, Queensland, Australia

ABSTRACT

Purple phototrophic bacteria have the ability to capture and use sunlight efficiently as an energy source. In these organisms, photosynthesis is carried out under anaerobic conditions. The introduction of oxygen into a culture growing phototrophically results in a rapid decrease in the synthesis of components of the photosynthetic apparatus and a change to an alternative source of energy, usually derived from the degradation of organic compounds under aerobic conditions (chemoheterotrophy). Switching back and forth between anaerobic (photosynthetic) and aerobic growth requires tight regulation of photosynthetic gene expression at the molecular level. Initial experiments by Cohen-Bazire et al. (1957) showed quite clearly that the regulation of photosynthetic gene expression was in response to two environmental stimuli. The most potent stimulus was oxygen; its presence shut down production of photosynthetic pigments very rapidly. To a lesser extent photosynthetic gene expression responded to light intensity. Low light intensity produced high levels of photosynthetic pigments; high light intensities caused a decrease, but the effect was less dramatic than that observed for oxygen. Since these initial observations were made in Rhodobacter sphaeroides some forty years ago, a great deal has been revealed as to the nature of the genes that encode the various components of the photosynthetic apparatus. Recent progress in the understanding of the regulation of expression of these genes in R. sphaeroides and Rhodobacter capsulatus is the subject of this review.

Alastair G. McEwan. Tel: +61 7 3365 4878. Fax: +61 7 3365 4620. e-mail: mcewan@biosci.uq.edu.au


Keywords: photosynthesis, purple bacteria, gene expression, oxygen-sensing, light-sensing




This article has been cited by other articles:


Home page
Plant Cell PhysiolHome page
H. Shimada, K. Ishida, Y. Machiya, and K.-i. Takamiya
Isolation of SIP, a Protein that Interacts with SPB, a Possible Transcriptional Regulatory Factor in Rhodobacter sphaeroides
Plant Cell Physiol., October 1, 2007; 48(10): 1504 - 1508.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
C. L. Tavano, J. C. Comolli, and T. J. Donohue
The role of dor gene products in controlling the P2 promoter of the cytochrome c2 gene, cycA, in Rhodobacter sphaeroides
Microbiology, June 1, 2004; 150(6): 1893 - 1899.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
A. T. Kovacs, G. Rakhely, and K. L. Kovacs
Genes Involved in the Biosynthesis of Photosynthetic Pigments in the Purple Sulfur Photosynthetic Bacterium Thiocapsa roseopersicina
Appl. Envir. Microbiol., June 1, 2003; 69(6): 3093 - 3102.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
L. Gomelsky, J. Sram, O. V. Moskvin, I. M. Horne, H. N. Dodd, J. M. Pemberton, A. G. McEwan, S. Kaplan, and M. Gomelsky
Identification and in vivo characterization of PpaA, a regulator of photosystem formation in Rhodobacter sphaeroides
Microbiology, February 1, 2003; 149(2): 377 - 388.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
J. C. Comolli, A. J. Carl, C. Hall, and T. Donohue
Transcriptional Activation of the Rhodobacter sphaeroides Cytochrome c2 Gene P2 Promoter by the Response Regulator PrrA
J. Bacteriol., January 15, 2002; 184(2): 390 - 399.
[Abstract] [Full Text] [PDF]


Home page
J. Bacteriol.Home page
S. Masuda, K. V. P. Nagashima, K. Shimada, and K. Matsuura
Transcriptional Control of Expression of Genes for Photosynthetic Reaction Center and Light-Harvesting Proteins in the Purple Bacterium Rhodovulum sulfidophilum
J. Bacteriol., May 15, 2000; 182(10): 2778 - 2786.
[Abstract] [Full Text]


Home page
J. Bacteriol.Home page
M. Gomelsky, I. M. Horne, H.-J. Lee, J. M. Pemberton, A. G. McEwan, and S. Kaplan
Domain Structure, Oligomeric State, and Mutational Analysis of PpsR, the Rhodobacter sphaeroides Repressor of Photosystem Gene Expression
J. Bacteriol., April 15, 2000; 182(8): 2253 - 2261.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
S. Ouchane and S. Kaplan
Topological Analysis of the Membrane-localized Redox-responsive Sensor Kinase PrrB from Rhodobacter sphaeroides 2.4.1
J. Biol. Chem., June 11, 1999; 274(24): 17290 - 17296.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Gomelsky and S. Kaplan
AppA, a Redox Regulator of Photosystem Formation in Rhodobacter sphaeroides 2.4.1, Is a Flavoprotein. IDENTIFICATION OF A NOVEL FAD BINDING DOMAIN
J. Biol. Chem., December 25, 1998; 273(52): 35319 - 35325.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1998 Society for General Microbiology.