Team:ETH Zurich/Biology/Validation

Sensor AlcR

Design of a AlcR/acetaldehyde repressed promoter P_AlcR

Because funghi activator normally does not work in e.coli, we modified AlcR in a way that it acts as a repressor. The mechanism of how AlcR activates transcription is not completely known what makes the process of redesigning it very challenging. For the promoter P_AlcR the operator site of AlcR from apergillus nidulans was placed between the -10 and -35 region of the bacterial promoter. As DNA targets we used two different versions, one with direct-repeat targets and one with inverted [4]. The idea is that in present of acetaldehyde AlcR will bind to the operon and block the binding of the RNA-polymerase. This only works if the mechanism of AlcR binding does not involves conformational changes or something similar.

Design of the promoter for the AlcR-system in SmoColi, the operon sequence is designed between the -10 and the -35 region (blue) of a strong promoter with inverted and direct-repeats.

Expression of AlcR in E.coli

Given that codon usage is not the same in E.coli and aspergillus nidulans, we analyzed codon usage of AlcR. We obtained a Codon adaptation index (CAI) of 0.7 for the aspergillus nidulans protein in E.coli, especially at the beginning of the gene a few very rare codons were included. To get a fully E.coli optimized Gen, we ordered the gene codon optimized. To make some first test, we exchanged the rare codons at the beginning of the aspergillus nidulans protein with PCR. With these protein we made same first Test of the expression of AlcR.

To test our designed AlcR-promotors the following system was designed (see Figure). In present of acetaldeyhde AlcR binds to the AlcR operon and inhibits the expression of GFP. For a better signal assam gfp was used.

Design of our testsystem.

results

To monitor the expression of AlcR a His-tag was introduced in the test system.

western blot

Sensor XylR

Xylene degradation

Bandpass

References