Translational_Unit

Part:BBa_K2483009

Designed by: Bryan Nowack   Group: iGEM17_Potsdam   (2017-10-19)
Revision as of 17:07, 19 October 2017 by Registry (Talk | contribs)

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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:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 2301
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 2301
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 2301
  • 25
    INCOMPATIBLE 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
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 3594
    Illegal BsaI.rc site found at 913


[edit]
Categories
//cds/biosynthesis
//function/biosynthesis
Parameters
chassisS.cerevisiae
input_sL-Tryptophan
outputIndolacetic Acid
proteinsIAAM/IAAH