Difference between revisions of "Part:BBa M50420:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | We codon optimized the amino acid sequence for E. coli. We did not make any other modifications from the source sequences. | + | We codon optimized the Cry11Aa amino acid sequence for E. coli. All of our parts were sourced from existing iGEM parts which are listed below. We did not make any other modifications from the source sequences. |
− | + | ||
Line 15: | Line 14: | ||
The source is previously established parts and the protein from uniprot cry11Aa. | The source is previously established parts and the protein from uniprot cry11Aa. | ||
− | Promoter: | + | Promoter: BBa_K914003 |
− | RBS: | + | RBS: BBa_B0034 |
− | Leader Sequence: | + | Leader Sequence: BBa_J32015 |
− | Gene: | + | Gene: BBa_K332011 codon optimized for E. coli |
− | 6x-His Tag: | + | 6x-His Tag: BBa_K1223006 |
− | Terminator: | + | Terminator: BBa_B0012 |
===References=== | ===References=== |
Revision as of 03:23, 12 June 2018
Mosquito Larvae Insecticide
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 188
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We codon optimized the Cry11Aa amino acid sequence for E. coli. All of our parts were sourced from existing iGEM parts which are listed below. We did not make any other modifications from the source sequences.
Source
The source is previously established parts and the protein from uniprot cry11Aa.
Promoter: BBa_K914003
RBS: BBa_B0034
Leader Sequence: BBa_J32015
Gene: BBa_K332011 codon optimized for E. coli
6x-His Tag: BBa_K1223006
Terminator: BBa_B0012