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Characterization by BOKU-Vienna 2017
For characterization the synGAL promoter was combined with GFP and the CYC1 terminator and afterwards integrated into the ura3 gene of Saccharomyces cerevisiae . The GFP fluorescence was measured using a flow cytometer after inducing with 3 different galactose concentrations (0,5%, 1% and 2%).
The cultivation was performded in 24 deepwell plates using 2 mL YP media. The preculture was performed in selective YPD. Prior to main culture inoculation the cells were washed twice in YP to remove remaining glucose. 100µL of 1mL preculture were used for inoculation of the main culture. As controls a wildtype and a clone expressing GFP under the constituve pTDH3 promoter were cultivated. In addition, the synGAL promoter without a Kozak sequence was investigated.
Results:
There is no significant difference between the different galactose concentrations which were investigated. The galpromoter combined with a Kozak sequnce showed the highes expression levels of GFP. It is about twice compared to the gal promoter without a Kozak sequence and three times higher compared to the pTDH3 promoter of Saccharomyces cerevisiae . The clones expressing GFP under the control of the consitutive TDH3 promoter were cultivated in YP + 2% glucose.