INVOLVEMENT OF SIGMA(54) IN EXPONENTIAL SILENCING OF THE PSEUDOMONAS-PUTIDA TOL PLASMID PU PROMOTER

Citation
I. Cases et al., INVOLVEMENT OF SIGMA(54) IN EXPONENTIAL SILENCING OF THE PSEUDOMONAS-PUTIDA TOL PLASMID PU PROMOTER, Molecular microbiology, 19(1), 1996, pp. 7-17
Citations number
62
Categorie Soggetti
Biology,Microbiology
Journal title
ISSN journal
0950382X
Volume
19
Issue
1
Year of publication
1996
Pages
7 - 17
Database
ISI
SICI code
0950-382X(1996)19:1<7:IOSIES>2.0.ZU;2-2
Abstract
The sigma(54)-dependent Pu promoter of the TOL plasmid pWWO of Pseudom onas putida becomes activated by the prokaryotic enhancer-binding XylR protein when cells encounter m-xylene in the medium. However, even in the presence of the aromatic inducer, Pu activity is silenced in vivo during rapid exponential growth of the cells in rich medium. Various elements known to be involved in the control of the transcriptional ac tivity of the promoter were examined to ascertain the mechanism by whi ch expression of Pu is limited during the exponential phase of growth. A truncated and fully constitutive XylR derivative deleted of its sig nal-reception N-terminal domain was found to be subjected to the same exponential silencing as the wildtype XylR when exposed to m-xylene. T his indicated that the phenomenon is not due to a late activation of X ylR by the aromatic effector. A Pu variant in which the integration ho st factor (IHF)-binding site had been functionally replaced by a stati cally curved DNA segment showed the same induction pattern, thus rulin g out variations in the intracellular levels of IHF changes during gro wth as the element responsible for the inactivity of Pu in rapidly gro wing cells. On the contrary, overproduction of the sigma(54) factor al lowed Pu expression during exponential phase. As sigma(54) protein lev els remained approximately constant during growth, the exponential sil encing of Pu could be caused ultimately by changes in the activity of the factor itself. This effect may not be exclusive to Pu, but could b e a general co-regulation mechanism in sigma(54)-dependent promoters t hat connects transcription of a specific set of genes with the general physiological status of the cells.