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