An E. coli cell-free expression toolbox: Application to synthetic gene circuits and artificial cells

Jonghyeon Shin, Vincent Noireaux

Research output: Contribution to journalArticlepeer-review

260 Scopus citations

Abstract

Cell-free protein synthesis is becoming a powerful technique to construct and to study complex informational processes in vitro. Engineering synthetic gene circuits in a test tube, however, is seriously limited by the transcription repertoire of modern cell-free systems, composed of only a few bacteriophage regulatory elements. Here, we report the construction and the phenomenological characterization of synthetic gene circuits engineered with a cell-free expression toolbox that works with the seven E. coli sigma factors. The E. coli endogenous holoenzyme E70 is used as the primary transcription machinery. Elementary circuit motifs, such as multiple stage cascades, AND gate and negative feedback loops are constructed with the six other sigma factors, two bacteriophage RNA polymerases, and a set of repressors. The circuit dynamics reveal the importance of the global mRNA turnover rate and of passive competition-induced transcriptional regulation. Cell-free reactions can be carried out over long periods of time with a small-scale dialysis reactor or in phospholipid vesicles, an artificial cell system. This toolbox is a unique platform to study complex transcription/translation-based biochemical systems in vitro.

Original languageEnglish (US)
Pages (from-to)29-41
Number of pages13
JournalACS Synthetic Biology
Volume1
Issue number1
DOIs
StatePublished - Jan 20 2012

Keywords

  • Cell-free gene circuits
  • Design principles
  • In vitro transcription-translation
  • Phospholipid vesicles

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