Difference between revisions of "Part:BBa K4825010:Design"

 
Line 17: Line 17:
  
 
===References===
 
===References===
 +
Sarah K. Hammer, Yanfei Zhang, and José L. Avalos
 +
ACS Synthetic Biology 2020 9 (3), 546-555
 +
DOI: 10.1021/acssynbio.9b00420

Revision as of 08:17, 12 October 2023


LEU2


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 637
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 637
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 637
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 637
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 637
    Illegal AgeI site found at 250
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

we engineered LEU1, LEU2, and LEU4 with three different signal peptide, which all lead them into mitochondria. Therefore, the concentration of enzymes that involve in 2-ketoacid elongation would become much higher in mitochondria, so that KIV will be convert to KIC before encountering KDC. In the end, KIC would be secreted out into cytosol and convert to Isopentanol


Source

Saccharomyces cerevisiae

References

Sarah K. Hammer, Yanfei Zhang, and José L. Avalos ACS Synthetic Biology 2020 9 (3), 546-555 DOI: 10.1021/acssynbio.9b00420