pBAD synthetic promoter library

As a tool for expressing lethal proteins in E. coli we made a synthetic promoter library (SPL, [http://dspace.mit.edu/handle/1721.1/60080 RFC 63]) with the pBAD arabinose inducible promoter. The concept was taken from the DTU iGEM team from 2010.

Methods

Experimental procedure

1. Random promoter sequences were ordered matching the sequence CTGACGNNNNNNNNNNNNNNNNNNTAWWATNNNNA.
2. USER cloning to add RFP downstream of promoter.
3. Colonies were plated.
4. Colonies that were not red prior to induction with arabinose but that did turn red after induction with arabinose were selected.
5. Wells were inoculated from overnight cultures of each of the selected colonies
6. One plate was run with arabinose, and another plate was run without arabinose.

Data analysis

1. Data was collected from the Biolector, and analyzed using a series of R scripts written by Chris Workman (unpublished).
   • The maturation and degradation times for mCherry were both assumed to be 40 min. TODOref
   • The growth rate, mu, was estimated to be 1.28 (from an average of all wells on all plates) since we expect each strain to grow at the same rate.
   • A time window representing exponential growth was selected (between 1 and 4.5 hours).
2. The RFP measurement for a constitutively expressed strain was used as a standard measure of growth. This is plotted on the x-axis in the detailed plots per colony below.
3. Figures were plotted using R.

Results

Summary

Details

Example of use

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See also "Hello World project".