Ontology highlight
ABSTRACT: Objective
The purpose of this project was to use an in vivo method to discover riboswitches that are activated by new ligands. We employed phage-assisted continuous evolution (PACE) to evolve new riboswitches in vivo. We started with one translational riboswitch and one transcriptional riboswitch, both of which were activated by theophylline. We used xanthine as the new target ligand during positive selection followed by negative selection using theophylline. The goal was to generate very large M13 phage populations that contained unknown mutations, some of which would result in new aptamer specificity. We discovered side products of three new theophylline translational riboswitches with different levels of protein production.Results
We used next generation sequencing to id
SUBMITTER: Shaver ZM
PROVIDER: S-EPMC6280357 | biostudies-literature | 2018 Dec
REPOSITORIES: biostudies-literature