JB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Marin, K.
Right arrow Articles by Hagemann, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Marin, K.
Right arrow Articles by Hagemann, M.
Journal of Bacteriology, June 2002, p. 2870-2877, Vol. 184, No. 11
0021-9193/02/$04.00+0     DOI: 10.1128/JB.184.11.2870-2877.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Salt-Dependent Expression of Glucosylglycerol-Phosphate Synthase, Involved in Osmolyte Synthesis in the Cyanobacterium Synechocystis sp. Strain PCC 6803{dagger}

Kay Marin, Jana Huckauf, Sabine Fulda, and Martin Hagemann*

Universität Rostock, FB Biowissenschaften, Pflanzenphysiologie, 18051 Rostock, Germany

Received 21 November 2001/ Accepted 28 February 2002

The cyanobacterium Synechocystis sp. strain PCC 6803 is able to acclimate to levels of salinity ranging from freshwater to twice the seawater concentrations of salt by accumulating the compatible solute glucosylglycerol (GG). Expression of the ggpS gene coding for the key enzyme (glucosylglycerol-phosphate synthase) in GG synthesis was examined in detail. Under control conditions, the GgpS protein is stable, so that weak constitutive transcription of the ggpS gene resulted in a significant protein content. However, the enzyme activity was biochemically switched off, and no GG was detectable. After a salt shock, an immediate increase in mRNA content proportional to the salt content occurred, while the GgpS protein and GG contents rose in a linear manner. Furthermore, the stability of the ggpS mRNA increased transiently. In salt-acclimated cells expression of the ggpS gene, the GgpS protein content, and the amount of accumulated GG depended linearly on the external salt concentration. Mapping of the 5' end of the ggpS transcript revealed a long nontranslated 5' sequence and a putative typical cyanobacterial promoter, which did not show any obvious salt-regulatory element. The alternative {sigma} factor {sigma}F was found to be involved in salt-dependent regulation of ggpS, since in a {sigma}F mutant induction of this gene was strongly reduced. The present study demonstrated that in addition to biochemical regulation of GgpS activity, alterations of ggpS expression are involved in regulation of GG synthesis in Synechocystis sp. strain PCC 6803. A model showing the interaction of the two regulatory levels is presented.


* Corresponding author. Mailing address: Universität Rostock, FB Biowissenschaften/Pflanzenphysiologie, Albert Einstein Str. 3a, D-18051 Rostock, Germany. Phone: 49-381-4986113. Fax: 49-381-4986112. E-mail: martin.hagemann{at}biologie.uni-rostock.de.

{dagger} This work is dedicated to Norbert Erdmann on his 65th birthday.


Journal of Bacteriology, June 2002, p. 2870-2877, Vol. 184, No. 11
0021-9193/02/$04.00+0     DOI: 10.1128/JB.184.11.2870-2877.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Appl. Environ. Microbiol. Infect. Immun. Eukaryot. Cell
Mol. Cell. Biol. J. Virol. Microbiol. Mol. Biol. Rev.
ALL ASM JOURNALS

Copyright © 2002 by the American Society for Microbiology. All rights reserved.