Dual transcriptional-translational cascade permits cellular level tuneable expression control.

Research output: Contribution to journalArticle

  • External authors:
  • Jayendra Shankar
  • Christopher Robinson
  • Samantha Halliwell
  • Lisa Butler
  • Mathew Upton


The ability to induce gene expression in a small molecule dependent manner has led to many applications in target discovery, functional elucidation and bio-production. To date these applications have relied on a limited set of protein-based control mechanisms operating at the level of transcription initiation. The discovery, design and reengineering of riboswitches offer an alternative means by which to control gene expression. Here we report the development and characterization of a novel tunable recombinant expression system, termed RiboTite, which operates at both the transcriptional and translational level. Using standard inducible promoters and orthogonal riboswitches, a multi-layered modular genetic control circuit was developed to control the expression of both bacteriophage T7 RNA polymerase and recombinant gene(s) of interest. The system was benchmarked against a number of commonly used E. coli expression systems, and shows tight basal control, precise analogue tunability of gene expression at the cellular level, dose-dependent regulation of protein production rates over extended growth periods and enhanced cell viability. This novel system expands the number of E. coli expression systems for use in recombinant protein production and represents a major performance enhancement over and above the most widely used expression systems.

Bibliographical metadata

Original languageEnglish
Article numbere21
JournalNucleic acids research
Issue number3
Early online date23 Sep 2015
StatePublished - 18 Feb 2016

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