Difference between revisions of "Part:BBa M50440:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | As this part was taken from previously described research, our design decisions were mostly left to address the induction of the protein and termination of translation. We chose GAL1 as our promoter because we were unsure of the toxicity the construct might have in the cell. This way, we were able to grow the cells up in glucose media, which inhibits GAL1, until we had robust colonies and were comfortable expressing the novel construct. | + | As this part was taken from previously described research, our design decisions were mostly left to address the induction of the protein and termination of translation. We chose GAL1 as our promoter because we were unsure of the toxicity the construct might have in the cell. This way, we were able to grow the cells up in glucose media, which inhibits GAL1, until we had robust colonies and were comfortable expressing the novel construct. The specific terminator was chosen because the codon was optimized for S. cerevisiae. The entire sequence was optimized for S. cerevisiae using the IDT Codon Optimization tool. |
===Source=== | ===Source=== | ||
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GAL1 promoter sequence: BBa_J63006 | GAL1 promoter sequence: BBa_J63006 | ||
| − | pHlash sequence: pHlash: A New Genetically Encoded and Ratiometric Luminescence Sensor of Intracellular pH, PLOS ( | + | pHlash sequence: pHlash: A New Genetically Encoded and Ratiometric Luminescence Sensor of Intracellular pH, PLOS (BBa_M50439) |
Terminator sequence: BBa_K1462070 | Terminator sequence: BBa_K1462070 | ||
Latest revision as of 11:48, 12 June 2018
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 150
Illegal AgeI site found at 759
Illegal AgeI site found at 1648 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1500
Illegal BsaI.rc site found at 1194
Illegal SapI.rc site found at 1513
Design Notes
As this part was taken from previously described research, our design decisions were mostly left to address the induction of the protein and termination of translation. We chose GAL1 as our promoter because we were unsure of the toxicity the construct might have in the cell. This way, we were able to grow the cells up in glucose media, which inhibits GAL1, until we had robust colonies and were comfortable expressing the novel construct. The specific terminator was chosen because the codon was optimized for S. cerevisiae. The entire sequence was optimized for S. cerevisiae using the IDT Codon Optimization tool.
Source
GAL1 promoter sequence: BBa_J63006
pHlash sequence: pHlash: A New Genetically Encoded and Ratiometric Luminescence Sensor of Intracellular pH, PLOS (BBa_M50439)
Terminator sequence: BBa_K1462070
References
https://parts.igem.org/Part:BBa_J63006
https://parts.igem.org/Part:BBa_K1462070
Zhang, Yunfei et al. “pHlash: A New Genetically Encoded and Ratiometric Luminescence Sensor of Intracellular pH.” Ed. Valentin Ceña. PLoS ONE 7.8 (2012): e43072. PMC. Web. 9 May 2018.