@inbook{8378d479a8734d1cb8a3c606d44db0ef,
title = "Using riboswitches to regulate gene expression and define gene function in mycobacteria",
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.",
keywords = "Flow cytometry, GFP, Homologous recombination, Inducible, Infection, Mycobacteria, Theophylline, β-Galactosidase",
author = "\{Van Vlack\}, \{Erik R.\} and Seeliger, \{Jessica C.\}",
note = "Publisher Copyright: {\textcopyright} 2015 Elsevier Inc. All rights reserved.",
year = "2015",
doi = "10.1016/bs.mie.2014.10.034",
language = "English",
series = "Methods in Enzymology",
publisher = "Academic Press Inc.",
pages = "251--265",
booktitle = "Methods in Enzymology",
}