Translational_Unit
Part:BBa_K2483009
Designed by: Bryan Nowack Group: iGEM17_Potsdam (2017-10-19)
IAAM and IAAH yeast optimized under GAL1 control
This part was used as a control for our liquid-liquid phase separation project. We used the CDS of the Indoleacetic acid-producing enzymes IAAM and IAAH from the part BBa_K515100 by Imperial College 2011 and codon optimized them for S.cerevisiae.
As a promoter, we used GAL1 (strong, galactose-induced promoter) and CYC1 as a terminator.
The CDS' are facing away from each other because of the way this part was assembled (we used Gibson Assembly) and the original structure of the plasmid (pYES2/CT).
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 2301
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 2301
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 2301
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 2301
Illegal NgoMIV site found at 1212
Illegal AgeI site found at 916
Illegal AgeI site found at 2086
Illegal AgeI site found at 2377 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 3594
Illegal BsaI.rc site found at 913
[edit]
Categories
Parameters
//cds/biosynthesis
//function/biosynthesis
//function/biosynthesis
chassis | S.cerevisiae |
input_s | L-Tryptophan |
output | Indolacetic Acid |
proteins | IAAM/IAAH |