Difference between revisions of "Part:BBa K1413002:Design"
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===Design Notes=== | ===Design Notes=== | ||
This part have been engineered in order to improve the signal of GFP afer induced transcription. | This part have been engineered in order to improve the signal of GFP afer induced transcription. | ||
− | It has been obtained by performing a mutation of 3 nucleotides within the sequence of RBS B0032. | + | It has been obtained by performing a mutation of 3 nucleotides within the sequence of RBS B0032.</br> |
− | RBS B0032 = tca<b>cac</b>aggaaag | + | RBS B0032 = tca<b>cac</b>aggaaag |
− | + | New RBS (SD 001) = tca<b>agg</b>aggaaag</br> | |
− | New RBS (SD 001) = tca<b>agg</b>aggaaag | + | |
This novel RBS sequence has been designed in accordance with the consensus Shine-Dalgarno sequence: AGGAGGUAA and allows the RNA to bind more tightly to the 16S ribosome to initiate translation. | This novel RBS sequence has been designed in accordance with the consensus Shine-Dalgarno sequence: AGGAGGUAA and allows the RNA to bind more tightly to the 16S ribosome to initiate translation. |
Revision as of 15:28, 31 October 2014
P0 promoter-RBS SD001-sfGFP- Terminator B0015 - Pr promoter-DmpR
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1241
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1719
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1404
Illegal BsaI.rc site found at 1945
Illegal SapI.rc site found at 211
Illegal SapI.rc site found at 2602
Design Notes
This part have been engineered in order to improve the signal of GFP afer induced transcription. It has been obtained by performing a mutation of 3 nucleotides within the sequence of RBS B0032.</br> RBS B0032 = tcacacaggaaag New RBS (SD 001) = tcaaggaggaaag</br>
This novel RBS sequence has been designed in accordance with the consensus Shine-Dalgarno sequence: AGGAGGUAA and allows the RNA to bind more tightly to the 16S ribosome to initiate translation.
Source
This part derives from BBa_K1413001.