This year Imperial College has added 45 new B.subtilis specific parts to the registry. In addition we sort to characterise some of these parts, including the constitutive promoter and ribosome binding site pveg-spoVG. The testing constructs we developed for this are shown below:
Summary of Data
The promoter and RBS combinations were characterised by measuring the expression of fluorescent proteins in B.subtilis. Cultures of B.subtilis transformed with the test constructs and non-transformed B.subtilis (control) were grown to the mid-log phase. Fluorescence and O.D.600 were both measured using a plate reader to generate fluorescence levels of the various samples. To make this data more generic the fluorescence data was normalized based on cell number using the O.D.600 and a calibration curve of O.D.600 vs colony forming units, as explained in the diagram below:
This calibration curve allowed us to produce the final data as shown below. This clearly shows B.subtilis transformed with biobricks GFP and RFP are fluorescing at the corresponding excitation and emission wavelengths.
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