Difference between revisions of "Part:BBa K4825026:Design"
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===References=== | ===References=== | ||
+ | "Chen, Y., Zhang, S., Young, E.M. et al. Genetic circuit design automation for yeast. Nat Microbiol 5, 1349–1360 (2020). https://doi.org/10.1038/s41564-020-0757-2. | ||
+ | |||
+ | Wei W, Shang Y, Zhang P, Liu Y, You D, Yin B, Ye B. Engineering Prokaryotic Transcriptional Activator XylR as a Xylose-Inducible Biosensor for Transcription Activation in Yeast. ACS Synth Biol. 2020 May 15;9(5):1022-1029. doi: 10.1021/acssynbio.0c00122. Epub 2020 Apr 17. PMID: 32268060." |
Revision as of 08:35, 12 October 2023
XylR-NLS
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 235
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
LEU2 is used as the yeast auxotrophic marker in this part, instead of normally URA3, which allows the co-transformation of the plasmid of this part and the plasmid of xylose promoters.
Source
Bacillus licheniformis
References
"Chen, Y., Zhang, S., Young, E.M. et al. Genetic circuit design automation for yeast. Nat Microbiol 5, 1349–1360 (2020). https://doi.org/10.1038/s41564-020-0757-2.
Wei W, Shang Y, Zhang P, Liu Y, You D, Yin B, Ye B. Engineering Prokaryotic Transcriptional Activator XylR as a Xylose-Inducible Biosensor for Transcription Activation in Yeast. ACS Synth Biol. 2020 May 15;9(5):1022-1029. doi: 10.1021/acssynbio.0c00122. Epub 2020 Apr 17. PMID: 32268060."