Difference between revisions of "Part:BBa K4825009:Design"
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===Source=== | ===Source=== | ||
− | Saccharomyces cerevisiae | + | <i>Saccharomyces cerevisiae</i> |
===References=== | ===References=== |
Latest revision as of 11:53, 12 October 2023
LEU1
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 643
Illegal EcoRI site found at 1432
Illegal PstI site found at 617
Illegal PstI site found at 1112
Illegal PstI site found at 1397 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 643
Illegal EcoRI site found at 1432
Illegal PstI site found at 617
Illegal PstI site found at 1112
Illegal PstI site found at 1397 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 643
Illegal EcoRI site found at 1432 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 643
Illegal EcoRI site found at 1432
Illegal PstI site found at 617
Illegal PstI site found at 1112
Illegal PstI site found at 1397 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 643
Illegal EcoRI site found at 1432
Illegal PstI site found at 617
Illegal PstI site found at 1112
Illegal PstI site found at 1397
Illegal NgoMIV site found at 160 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 1622
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