Literature DB >> 10913697

Analysis of the dormancy-inducible narK2 promoter in Mycobacterium bovis BCG.

B Hutter1, T Dick.   

Abstract

Upon depletion of oxygen, the obligate aerobe mycobacteria switch from growth to a state of non-replicating persistence or dormancy. Here, we report the first functional analysis of a dormancy-dependent mycobacterial promoter in Mycobacterium bovis BCG. Promoter probing using a 'lacZ reporter detected a dormancy-inducible promoter activity upstream of the coding sequence for the putative nitrite extrusion protein NarK2. Primer extension analysis mapped a transcriptional start point 47 bp upstream of the narK2 start codon. Deletion analysis revealed that the sequence -222 to -133 bp upstream from the transcriptional start point was required for basal and dormancy-inducible reporter expression. The sequence +1 to +47 downstream of the transcriptional start point had a strong inhibitory effect on the level of dormancy-induced beta-galactosidase activity. The identification of apparent activating and inhibiting regions suggests that the narK2 promoter is at least under dual control.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10913697     DOI: 10.1111/j.1574-6968.2000.tb09185.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  16 in total

1.  Proteins of Mycobacterium bovis BCG induced in the Wayne dormancy model.

Authors:  C Boon; R Li; R Qi; T Dick
Journal:  J Bacteriol       Date:  2001-04       Impact factor: 3.490

2.  Mycobacterium bovis BCG response regulator essential for hypoxic dormancy.

Authors:  Calvin Boon; Thomas Dick
Journal:  J Bacteriol       Date:  2002-12       Impact factor: 3.490

3.  Compiling a molecular inventory for Mycobacterium bovis BCG at two growth rates: evidence for growth rate-mediated regulation of ribosome biosynthesis and lipid metabolism.

Authors:  D J V Beste; J Peters; T Hooper; C Avignone-Rossa; M E Bushell; J McFadden
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

4.  Multifunctional T Cell Response to DosR and Rpf Antigens Is Associated with Protection in Long-Term Mycobacterium tuberculosis-Infected Individuals in Colombia.

Authors:  Leonar Arroyo; Mauricio Rojas; Kees L M C Franken; Tom H M Ottenhoff; Luis F Barrera
Journal:  Clin Vaccine Immunol       Date:  2016-10-04

5.  Dependence of Mycobacterium bovis BCG on anaerobic nitrate reductase for persistence is tissue specific.

Authors:  Christian Fritz; Silvia Maass; Andreas Kreft; Franz-Christoph Bange
Journal:  Infect Immun       Date:  2002-01       Impact factor: 3.441

Review 6.  Latent tuberculosis infection: myths, models, and molecular mechanisms.

Authors:  Noton K Dutta; Petros C Karakousis
Journal:  Microbiol Mol Biol Rev       Date:  2014-09       Impact factor: 11.056

7.  Mycobacteria Manipulate G-Protein-Coupled Receptors to Increase Mucosal Rac1 Expression in the Lungs.

Authors:  Nader Alaridah; Nataliya Lutay; Erik Tenland; Anna Rönnholm; Oskar Hallgren; Manoj Puthia; Gunilla Westergren-Thorsson; Gabriela Godaly
Journal:  J Innate Immun       Date:  2016-12-24       Impact factor: 7.349

8.  Portrait of a pathogen: the Mycobacterium tuberculosis proteome in vivo.

Authors:  Nicole A Kruh; Jolynn Troudt; Angelo Izzo; Jessica Prenni; Karen M Dobos
Journal:  PLoS One       Date:  2010-11-11       Impact factor: 3.240

9.  A family of acr-coregulated Mycobacterium tuberculosis genes shares a common DNA motif and requires Rv3133c (dosR or devR) for expression.

Authors:  Matthew A Florczyk; Lee Ann McCue; Anjan Purkayastha; Egidio Currenti; Meyer J Wolin; Kathleen A McDonough
Journal:  Infect Immun       Date:  2003-09       Impact factor: 3.441

10.  Regulation of expression of mas and fadD28, two genes involved in production of dimycocerosyl phthiocerol, a virulence factor of Mycobacterium tuberculosis.

Authors:  Tatiana D Sirakova; Ann Marie Fitzmaurice; Pappachan Kolattukudy
Journal:  J Bacteriol       Date:  2002-12       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.