Difference between revisions of "Part:BBa K2333441:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | of | + | Parts of this had to be ordered as a G-block and was assembled via Gibson Assembly. |
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===Source=== | ===Source=== | ||
− | + | The CueR and PcopA sequences were taken from E. coli. CueR was codon optimized. | |
+ | |||
+ | Pdt E was originally generated by mutagenesis from the endogenous Lon degraded tags from the bacteria Mycoplasma florum by Collins et al. 2014 "Tunable Protein Degradation in Bacteria". Pdt E corresponds to Collins et al.'s tag pdt#3d. To create pdt E, the amino acid sequence was taken from Collins et al. and was codon optimized for E. coli, then synthesized by IDT. | ||
+ | |||
+ | UNS sequences are from Torella, J. P., Boehm, C. R., Lienert, F., Chen, J. H., Way, J. C., & Silver, P. A. (2013). Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly. | ||
+ | |||
===References=== | ===References=== |
Revision as of 23:53, 29 October 2017
Copper sensor with Protein Degradation Tag E
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1229
Illegal AgeI site found at 1341 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Parts of this had to be ordered as a G-block and was assembled via Gibson Assembly.
Source
The CueR and PcopA sequences were taken from E. coli. CueR was codon optimized.
Pdt E was originally generated by mutagenesis from the endogenous Lon degraded tags from the bacteria Mycoplasma florum by Collins et al. 2014 "Tunable Protein Degradation in Bacteria". Pdt E corresponds to Collins et al.'s tag pdt#3d. To create pdt E, the amino acid sequence was taken from Collins et al. and was codon optimized for E. coli, then synthesized by IDT.
UNS sequences are from Torella, J. P., Boehm, C. R., Lienert, F., Chen, J. H., Way, J. C., & Silver, P. A. (2013). Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly.