| Literature DB >> 18689485 |
Johannes Amon1, Tanja Bräu, Aletta Grimrath, Eva Hänssler, Kristin Hasselt, Martina Höller, Nadja Jessberger, Lisa Ott, Juraj Szököl, Fritz Titgemeyer, Andreas Burkovski.
Abstract
The effect of nitrogen regulation on the level of transcriptional control has been investigated in a variety of bacteria, such as Bacillus subtilis, Corynebacterium glutamicum, Escherichia coli, and Streptomyces coelicolor; however, until now there have been no data for mycobacteria. In this study, we found that the OmpR-type regulator protein GlnR controls nitrogen-dependent transcription regulation in Mycobacterium smegmatis. Based on RNA hybridization experiments with a wild-type strain and a corresponding mutant strain, real-time reverse transcription-PCR analyses, and DNA binding studies using cell extract and purified protein, the glnA (msmeg_4290) gene, which codes for glutamine synthetase, and the amtB (msmeg_2425) and amt1 (msmeg_6259) genes, which encode ammonium permeases, are controlled by GlnR. Furthermore, since glnK (msmeg_2426), encoding a PII-type signal transduction protein, and glnD (msmeg_2427), coding for a putative uridylyltransferase, are in an operon together with amtB, these genes are part of the GlnR regulon as well. The GlnR protein binds specifically to the corresponding promoter sequences and functions as an activator of transcription when cells are subjected to nitrogen starvation.Entities:
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Year: 2008 PMID: 18689485 PMCID: PMC2580704 DOI: 10.1128/JB.00855-08
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490