Device
Part:BBa_K1475009:Design
Designed by: Daniel Weltz Pedersen Group: iGEM14_SDU-Denmark (2014-10-07)
Limonene synthase with tet promoter, RBS and terminator
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 178
Design Notes
The device was constructed using standard assembly from the p(TetR) repressible promoter Part:BBa_R0040 and a LIMS1 translational unit Part:BBa_I742111
LIMS1: Due to the natural sequence containing several forbidden restriction sites some codons was mutated silently to make the sequence compliant with the BioBrick standard during the initial design of the LIMS1 basic part (Part:BBa_I742110).
Source
Organizm: Citrus limon
References
1. UniProt, accession number: Q8L5K3. http://www.uniprot.org/uniprot/Q8L5K3
2. BRENDA, 2014: EC 4.2.3.20 - (R)-limonene synthase. http://www.brenda-enzymes.org/enzyme.php?ecno=4.2.3.20&Suchword=&organism%5B%5D=Citrus+limon&show_tm=0