Regulatory
Part:BBa_K1351038:Design
Designed by: Nikolai Peschek Group: iGEM14_LMU-Munich (2014-10-06)
P3-promoter
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Several mutated illegal restriction sites. The mutated codons have been optimized regarding the codon usage of Bacillus subtilis.
Source
This part was generated by amplification from artificially synthesized DNA with the primers listed below, followed by digestion with EcoRI and PstI and ligation into pSB1C3.
P3_fwd: GATCGAATTCGCGGCCGCTTCTAGAGGTACAATCTTTTATCATTATATTGCCTAAC
P3_rev: GATCACTAGTACTCTGTGATCTAGTTATATTAAAACATGC
Annealing sequences are written in bold.
References
Reynolds, J. and S. Wigneshweraraj (2011). "Molecular Insights into the Control of Transcription Initiation at the Staphylococcus aureus agr operon." Journal of Molecular Biology 412(5): 862-881.