Development of a Bacillus subtilis cell-free transcription-translation system for prototyping regulatory elements

Cell-free transcription-translation systems were originally applied towards in vitro protein production. More recently, synthetic biology is enabling these systems to be used within a systematic design context for prototyping DNA regulatory elements, genetic logic circuits and biosynthetic pathways....

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Veröffentlicht in:Metabolic engineering 2016-11, Vol.38, p.370-381
Hauptverfasser: Kelwick, Richard, Webb, Alexander J., MacDonald, James T., Freemont, Paul S.
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Sprache:eng
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Zusammenfassung:Cell-free transcription-translation systems were originally applied towards in vitro protein production. More recently, synthetic biology is enabling these systems to be used within a systematic design context for prototyping DNA regulatory elements, genetic logic circuits and biosynthetic pathways. The Gram-positive soil bacterium, Bacillus subtilis, is an established model organism of industrial importance. To this end, we developed several B. subtilis-based cell-free systems. Our improved B. subtilis WB800N-based system was capable of producing 0.8µM GFP, which gave a ~72x fold-improvement when compared with a B. subtilis 168 cell-free system. Our improved system was applied towards the prototyping of a B. subtilis promoter library in which we engineered several promoters, derived from the wild-type Pgrac (σA) promoter, that display a range of comparable in vitro and in vivo transcriptional activities. Additionally, we demonstrate the cell-free characterisation of an inducible expression system, and the activity of a model enzyme - renilla luciferase. •Several B. subtilis cell-free transcription-translation systems have been developed.•B. subtilis WB800N cell-free system ~72× more active than B. subtilis 168 system.•Comparability between in vitro and in vivo characterised regulatory elements.•Characterised an inducible expression system for genetic circuit applications.•Applied to measure the activity of the model enzyme Renilla luciferase.
ISSN:1096-7176
1096-7184
DOI:10.1016/j.ymben.2016.09.008