Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6494212 | Metabolic Engineering | 2016 | 12 Pages |
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 0.8 µM 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 (ÏA) 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.
Keywords
Bacillus subtilistRNACTPGTPUTPCOA3-PGADTTPromoter library3-phosphoglyceratecAMPadenosine 3′,5′-cyclic monophosphateAdenosine TriphosphateATPLuciferase assaytransfer ribonucleic acidUridine triphosphatedithiothreitolSynthetic biologyCytidine triphosphateMagnesiumNADNicotinamidePotassiumcoenzyme AGuanosine triphosphate
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Bioengineering
Authors
Richard Kelwick, Alexander J. Webb, James T. MacDonald, Paul S. Freemont,