Types | DnaRegion
|
Roles | Composite
engineered_region
|
Sequences | BBa_K510016_sequence (Version 1)
|
Description
The mini-Tn7-Gm-pBad/araC artificial transposon has been constructed based on pUC18R6KT-miniTn7-Gm (BBa_K510012) by inserting a pBad/araC promoter(BBa_I0500) in its BioBrick cloning site (BCS). This plasmid can be used as inducible expression vector in single copy by integrating the device in the genome of the working organism.
Notes
The BBa_I0500 BioBrick was inserted within the BCS of pUC18R6KT-miniTn7BB-Gm by EcoRI and PstI clonning.
Source
The pUC18R6KT vector was amplified by PCR using as template a pTNS2 plasmid (GenBank accession number: AY884833) provided by Herbert P. Schweizer. The primers were designed to flanked the pUC18R6KT with SfiI restriction sites and allow the insertion of the mini-Tn7-Gm. Primers: attcGGCCTAGGCGGCCgtcgttttacaacgtcgtgac and attcGGCCGCCTAGGCCggaagcataaagtgtaaagcctg. The miniTn7BB-Gm minitransposon was synthesized commercially, and then digested at the flanking SfiI sites and cloned into SfiI-digested pUC18R6KT PCR products.