Tunable Gene Expression System Independent of Downstream Coding Sequence

ACS Synth Biol. 2020 Nov 20;9(11):2998-3007. doi: 10.1021/acssynbio.0c00029. Epub 2020 Oct 14.

Abstract

Fine control of the expression levels of proteins constitutes a major challenge in synthetic biology and metabolic engineering. However, the dependence of translation initiation on the downstream coding sequence (CDS) obscures accurate prediction of the protein expression levels from mRNA sequences. Here, we present a tunable gene-expression system comprising 24 expression cassettes that produce predefined relative expression levels of proteins ranging from 0.001 to 1 without being influenced by the downstream CDS. To validate the practical utility of the tunable expression system, it was applied to a synthetic circuit displaying three states of fluorescence depending on the difference in protein expression levels. To demonstrate the suitability of application to metabolic engineering, this system was used to diversify the levels of key metabolic enzymes. As a result, expression-optimized strains were capable of producing 2.25 g/L of cadaverine, 2.59 g/L of L-proline, and 95.7 mg/L of 1-propanol. Collectively, the tunable expression system could be utilized to optimize genetic circuits for desired operation and to optimize metabolic fluxes through biosynthetic pathways for enhancing production yields of bioproducts. This tunable system will be useful for studying basic and applied biological sciences in addition to applications in synthetic biology and metabolic engineering.

Keywords: metabolic engineering; protein expression; synthetic biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biochemical Phenomena / genetics
  • Escherichia coli / genetics
  • Gene Expression / genetics*
  • Gene Expression Regulation, Bacterial / genetics
  • Gene Regulatory Networks / genetics
  • Metabolic Engineering / methods
  • Open Reading Frames / genetics*
  • Synthetic Biology / methods