| Literature DB >> 25605389 |
Erik R Van Vlack1, Jessica C Seeliger2.
Abstract
Mycobacteria include both environmental species and many pathogenic species such as Mycobacterium tuberculosis, an intracellular pathogen that is the causative agent of tuberculosis in humans. Inducible gene expression is a powerful tool for examining gene function and essentiality, both in in vitro culture and in host cell infections. The theophylline-inducible artificial riboswitch has recently emerged as an alternative to protein repressor-based systems. The riboswitch is translationally regulated and is combined with a mycobacterial promoter that provides transcriptional control. We here provide methods used by our laboratory to characterize the riboswitch response to theophylline in reporter strains, recombinant organisms containing riboswitch-regulated endogenous genes, and in host cell infections. These protocols should facilitate the application of both existing and novel artificial riboswitches to the exploration of gene function in mycobacteria.Entities:
Keywords: Flow cytometry; GFP; Homologous recombination; Inducible; Infection; Mycobacteria; Theophylline; β-Galactosidase
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Year: 2014 PMID: 25605389 PMCID: PMC5154175 DOI: 10.1016/bs.mie.2014.10.034
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600