Difference between revisions of "Part:BBa K2753002:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | The geranyl pyrophosphate synthase gene was codon optimised for E. coli. | |
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===Source=== | ===Source=== | ||
− | + | The sequence of this part was originally obtained from NCBI then was synthesised by GenScript | |
===References=== | ===References=== | ||
+ | |||
+ | Alonso-gutierrez, J., Chan, R., Batth, T. S., Adams, P. D., Keasling, J. D., Petzold, C. J., & Soon, T. (2013). Metabolic engineering of Escherichia coli for limonene and perillyl alcohol production. Metabolic Engineering, 19, 33–41. https://doi.org/10.1016/j.ymben.2013.05.004 |
Latest revision as of 07:32, 17 October 2018
pSB1C3-GPPS cds
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The geranyl pyrophosphate synthase gene was codon optimised for E. coli.
Source
The sequence of this part was originally obtained from NCBI then was synthesised by GenScript
References
Alonso-gutierrez, J., Chan, R., Batth, T. S., Adams, P. D., Keasling, J. D., Petzold, C. J., & Soon, T. (2013). Metabolic engineering of Escherichia coli for limonene and perillyl alcohol production. Metabolic Engineering, 19, 33–41. https://doi.org/10.1016/j.ymben.2013.05.004