Difference between revisions of "Part:BBa K2938000:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | Designed by our lab prior to the competition with a single point mutation to slow down initial translation initiation rates. | |
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Schlesinger, Orr, et al. "Tuning of recombinant protein expression in Escherichia coli by manipulating transcription, translation initiation rates, and incorporation of noncanonical amino acids." ACS synthetic biology 6.6 (2017): 1076-1085. | Schlesinger, Orr, et al. "Tuning of recombinant protein expression in Escherichia coli by manipulating transcription, translation initiation rates, and incorporation of noncanonical amino acids." ACS synthetic biology 6.6 (2017): 1076-1085. | ||
https://www.biorxiv.org/content/10.1101/100982v1.full | https://www.biorxiv.org/content/10.1101/100982v1.full | ||
+ | |||
+ | Shin, Jonghyeon, and Vincent Noireaux. "Efficient cell-free expression with the endogenous E. Coli RNA polymerase and sigma factor 70." Journal of biological engineering 4.1 (2010): 8. |
Latest revision as of 13:17, 4 October 2019
Attenuated pBEST-PR promoter after point mutation
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 56
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Designed by our lab prior to the competition with a single point mutation to slow down initial translation initiation rates.
Source
This promoter was already in use in our lab.
References
Schlesinger, Orr, et al. "Tuning of recombinant protein expression in Escherichia coli by manipulating transcription, translation initiation rates, and incorporation of noncanonical amino acids." ACS synthetic biology 6.6 (2017): 1076-1085. https://www.biorxiv.org/content/10.1101/100982v1.full
Shin, Jonghyeon, and Vincent Noireaux. "Efficient cell-free expression with the endogenous E. Coli RNA polymerase and sigma factor 70." Journal of biological engineering 4.1 (2010): 8.