Dynamic Control of Gene Expression with Riboregulated Switchable Feedback Promoters

Cameron J. Glasscock, Bradley W. Biggs, John T. Lazar, Jack H. Arnold, Lisa A. Burdette, Aliki Valdes, Min Kyoung Kang, Danielle Tullman-Ercek*, Keith E.J. Tyo*, Julius B. Lucks*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

One major challenge in synthetic biology is the deleterious impacts of cellular stress caused by expression of heterologous pathways, sensors, and circuits. Feedback control and dynamic regulation are broadly proposed strategies to mitigate this cellular stress by optimizing gene expression levels temporally and in response to biological cues. While a variety of approaches for feedback implementation exist, they are often complex and cannot be easily manipulated. Here, we report a strategy that uses RNA transcriptional regulators to integrate additional layers of control over the output of natural and engineered feedback responsive circuits. Called riboregulated switchable feedback promoters (rSFPs), these gene expression cassettes can be modularly activated using multiple mechanisms, from manual induction to autonomous quorum sensing, allowing control over the timing, magnitude, and autonomy of expression. We develop rSFPs in Escherichia coli to regulate multiple feedback networks and apply them to control the output of two metabolic pathways. We envision that rSFPs will become a valuable tool for flexible and dynamic control of gene expression in metabolic engineering, biological therapeutic production, and many other applications.

Original languageEnglish (US)
Pages (from-to)1199-1213
Number of pages15
JournalACS synthetic biology
Volume10
Issue number5
DOIs
StatePublished - May 21 2021

Funding

The authors gratefully acknowledge Dr. Ryan Philippe for careful reading of the manuscript, the gift of E. coli Tax1 and plasmids p5Trc and p10Trc from Manus Bio, and Taylor Nichols for helpful discussions. The pOSIP plasmid kit used for clonetegration was a gift from Drew Endy and Keith Shearwin (Addgene kit # 1000000035). E. coli DH1, pP -MevT-MBIS, and pTrc-ADS were gifts from Jay Keasling. pTHSSe_59 was a gift from Christopher Voigt (Addgene plasmid # 109253; http://n2t.net/addgene:109253 ; RRID: Addgene 109253). This work was supported by an NSF CAREER award (1452441 to J.B.L.), an NSF CBET award (1803747 to J.B.L., K.E.J.T. and D.T.-E.), an NSF Graduate Research Fellowship (DGE-1144153 to C.J.G.), an NIH Biotechnology Training Grant (T32-GM008449-23 to B.W.B.) and an NSF Synthetic Biology REU (DBI-1757973 to A.V.). gadE

Keywords

  • RNA
  • feedback
  • gene regulation
  • isoprenoids
  • metabolic engineering
  • quorum-sensing

ASJC Scopus subject areas

  • Biomedical Engineering
  • Biochemistry, Genetics and Molecular Biology (miscellaneous)

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