Team:Johns Hopkins-Wetware/Parts

We constructed and submitted three vectors that can easily convert our Yeast Golden Gate Parts into BioBricks. These conversion vectors consist of the pSB1C3 standard BioBrick backbone and also contain RFP (BBa_J04450) for easy red/white screening. We have inserted BsaI sites flanking the RFP gene. BsaI digestion exposes the signature overhangs corresponding to a promoter, coding sequence, or terminator (BBa_K799024, BBa_K799025, BBa_K799024). In a one-pot digestion-ligation reaction, Yeast Golden Gate Parts can be converted to BioBricks through a red/white selection.

We have sequenced these vectors across the RFP insert to verify the signature overhang and BsaI sequences. Using these new vectors, have also performed one-pot digestion ligation reactions to successfully convert 5 promoters, 2 ORFs, and 1 terminator sequence into BioBrick-compatible parts.

We BioBricked 5 ethanol-induced yeast promoters with varying induction levels (BBa_K799001, BBa_K799003, BBa_K799005, BBa_K799007, BBa_K799009), the human cytochrome p450 2E1 (CYP2E1) used in our ethanol-control project (BBa_K799027), and the yeast terminator from the MFA2 gene (BBa_K799029). We also BioBricked a GFP sequence lacking BsaI and BsmBI sites for use with Yeast Golden Gate (BBa_K799028). We have sequence verified all of these parts. The ethanol-inducible promoters have been characterized through GFP expression under various ethanol levels. We have tested the ability of CYP2E1 to reduce ethanol concentration over a 24 hour fermentation.

In the first iteration of our BioParts course, we generated around 850 yeast parts including promoters, coding sequences, and terminators. These are parts that can be converted to the BioBrick standard using our conversion vectors above.