Coding
Part:BBa_K777100:Design
Designed by: Team Goettingen Group: iGEM12_Goettingen (2012-09-15)
flhDC
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 609
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
- The PstI restriction site was mutated to CTGCGG using the reverse primer.
- flhDC was amplified from genomic DNA of E. coli DH10B via PCR using the following primers:
- Fwd: ACTGAATTCGCGGCCGCTTCTAGATGCATACCTCCGAGTTGCTG
- Rev: TCCTGCAGCGGCCGCTACTAGTTACTGCCCGGGATGGCGGTTGACATAAGCcGCAGGCAAAGCTGCCAACAG
(the uncapitalized "c" induces the mutation for removal of the PstI site)
- Fwd: ACTGAATTCGCGGCCGCTTCTAGATGCATACCTCCGAGTTGCTG
Source
- The part was amplified from genomic DNA of E. coli str. K-12 substr. DH10B, complete genome (CP000948.1).
References
- Chevance F.F., Hughes K.T. Coordinating assembly of a bacterial macromolecular machine. Nat Rev Microbiol. 2008. 6:455–465.
- Ling H., Kang A., Tan M.H., Qi X., Chang M.W. The absence of the luxS gene Increases swimming motility and flagella synthesis in Escherichia coli K12. Biochem Biophys Res Commun. 2010. 401: 521-526.