Identification of the Mycobacterium tuberculosis GlnE promoter and its response to nitrogen availability.

Carey A Pashley, Amanda C Brown, Dina Robertson, Tanya Parish
Author Information
  1. Carey A Pashley: Centre for Infectious Disease, Institute for Cell and Molecular Science, Barts and the London, London E1 2AT, UK.
  2. Amanda C Brown: Centre for Infectious Disease, Institute for Cell and Molecular Science, Barts and the London, London E1 2AT, UK.
  3. Dina Robertson: Centre for Infectious Disease, Institute for Cell and Molecular Science, Barts and the London, London E1 2AT, UK.
  4. Tanya Parish: Centre for Infectious Disease, Institute for Cell and Molecular Science, Barts and the London, London E1 2AT, UK.

Abstract

Adenylyltransferase, GlnE, has a predicted role in controlling the enzymic activity of glutamine synthetase, the key enzyme in ammonia assimilation. It was previously demonstrated that glnE is an essential gene in Mycobacterium tuberculosis. glnE is located downstream of glnA2, one of four glutamine synthetases. The expression of GlnE under various conditions was determined. Although a co-transcript of glnA2 and glnE was detectable, the major transcript was monocistronic. A transcriptional start site immediately upstream of glnE was identified and it was shown by site-directed mutagenesis that the predicted -10 region is a functional promoter. It was demonstrated that in a Mycobacterium smegmatis background M. tuberculosis P(glnE) was up-regulated in ammonia- or glutamine-containing media.

Grants

  1. 063894/Wellcome Trust

MeSH Term

Gene Expression Regulation, Bacterial
Genes, Bacterial
Genes, Essential
Mutagenesis, Site-Directed
Mycobacterium tuberculosis
Nitrogen
Nucleotidyltransferases
Promoter Regions, Genetic
Up-Regulation

Chemicals

Nucleotidyltransferases
glutamine-synthetase adenylyltransferase
Nitrogen

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