Part:BBa_K627011:Design
Fusion part of pBAD arabinose-inducible induction system and the HRV 14_3C protease
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1523
Illegal BglII site found at 1711
Illegal BamHI site found at 1144 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1239
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 961
Design Notes
This biobrick was built by PCR using the following PCR primers:
Site directed mutagenesis of HRV 14 3C protease:
Fragment 1:
- f_14_3C_iGEM: ATATAGAATTCGCGGCCGCTTCTAGATGGGACCAAACACAGAATTTGCACTATCC
- r_14_3C_ACCAGC: ACCATTTGCTGGTACATCATCACCAGG
Fragment 2:
- f_14_3C_ACCAGC: CCTGGTGATGATGTACCAGCAAATGGT
- r_14_3C_tm_XbaI208_A-T: CACTGTAAGCTCAAGATTAATGTTCTC
Fragment 3:
- f_14_3C_tm_Xba208_A-T: GAGAACATTAATCTTGAGCTTACAGTG
- r_14_3C_tm_XbaI280_A-T: ATCCACACCTTCGAGATCTTCTGATAT
Fragment 4:
- f_14_3C_tm_Xba280_A-T: ATATCAGAAGATCTCGAAGGTGTGGAT
- r_14_3C_iGEM_BamHI: ATATAGGATCCACTGCAGCGGCCGCTACTAGTTTTGTTTCTCTACAAAATATTGTTTTTTAAGTTGAGCTGA
Primers used for first assembly PCR of mutated fragments:
Fragment 5, containing Fragment 1 and 2:
- f_14_3C_iGEM: ATATAGAATTCGCGGCCGCTTCTAGATGGGACCAAACACAGAATTTGCACTATCC
- r_14_3C_tm_Xba208_A-T: CACTGTAAGCTCAAGATTAATGTTCTC
Fragment 6, containing Fragment 3 and 4:
- f_14_3C_tm_Xba208_A-T: GAGAACATTAATCTTGAGCTTACAGTG
- r_14_3C_iGEM_BamHI: ATATAGGATCCACTGCAGCGGCCGCTACTAGTTTTGTTTCTCTACAAAATATTGTTTTTTAAGTTGAGCTGA
Primer used for final assembly PCR of mutated fragments:
Complete mutated 14_3C protease, containing Fragment 5 and 6:
- f_14_3C_iGEM: ATATAGAATTCGCGGCCGCTTCTAGATGGGACCAAACACAGAATTTGCACTATCC
- r_14_3C_iGEM_BamHI: ATATAGGATCCACTGCAGCGGCCGCTACTAGTTTTGTTTCTCTACAAAATATTGTTTTTTAAGTTGAGCTGA
Primers used for amplification of the pBAD arabinose-inducible induction system:
- f_AraC_iGEM_HindIII: TATAAGCTTGAATTCGCGGCCGCTTCTAGATTATGACAACTTGACGGCTACATCATT
- r_AraC_NgoMIV: ATAGCCGGCCTCCTTCTTAAAGTTAAACAAAATTATTTCTAGCCC
Primers used for amplification and modification of HRV 14 3C protease:
- f_14_3C_AraFusion_NgoMIV: ATATTGCCGGCATGGGACCAAACACAGAATTTGCACTATCC
- r_14_3C_iGEM_BamHI: ATATAGGATCCACTGCAGCGGCCGCTACTAGTTTTGTTTCTCTACAAAATATTGTTTTTTAAGTTGAGCTGA
Source
TorA signal sequence and the lactamase was amplified via PCR from pJC354, which originates from two iGEM compatible BioBricks: BBa_K208005 and BBa_I757010. The cleavage site was created, based on the information of the Brenda enzymes database, via 2 oligonucleotides ordered from Sigma-Aldrich.
References
Used parts from the Registry of Standard Biological Parts:
- BBa_K208005
- BBa_I757010