| Literature DB >> 27697563 |
Richard Kelwick1, Alexander J Webb1, James T MacDonald1, Paul S Freemont2.
Abstract
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.Entities:
Keywords: Bacillus subtilis; Cell-free transcription-translation; Luciferase assay; Promoter library; Regulatory element prototyping; Synthetic biology
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Year: 2016 PMID: 27697563 DOI: 10.1016/j.ymben.2016.09.008
Source DB: PubMed Journal: Metab Eng ISSN: 1096-7176 Impact factor: 9.783