Construction of pTetFlp

From 2009.igem.org

Strategy for deletion of Rha-RedRecA and dhfr

Figure:1

As shown above the kan.gcc which encodes for kanamycin resistance was amplified from the Pirate-km.gcs plasmid (from Stewart lab). This Kan gene has homology arms to enable its introduction into the pRedFlp plasmid (from Stewart lab) by Red/ET recombination. The pTetFlp KanR has a pSC101 temperature sensitive origin (grows at 30°C but not at 37°C). The PCR product was isolated and purified from the gel. The gel was as shown below

PCR product of pR6K-KanR.JPG

Red/ET was done to introduce the KanR gene into the pTetFlp. The resulting plasmid was named pTetFlp KanR. This was digested with PstI, and showed the following results

PTetFlp-KanR, digested with Pst I.JPG

From the 14 minis, 3 correct clones were re-electroporated, in order to purify it. This is a high copy plasmid and the first step of Red/Et mostly results in a mixture of the original plasmid and the desired plasmid. Re-electroporation and transformation results in purer products. 16 minis were done, of which 13 were correct, as shown below

Re-electroporation of pTetFlp-KanR with Pst I and EcoRI digest.JPG

Strategy for insertion of Flp reporter

Figure:2

As shown in the strategy above, pTetFlp KanR was digested using XhoI in order to linearize it.

F3-ZeoR-F3-RFP (plasmid ordered from GeneArt), is as shown in Fig 3. This when digested using PvuII resulted in the fragment shown in Fig 4. It carries a zeocin resistance gene (ZeoR). The ZeoR gene is flanked by F3 sites that are similar to the FRT sites (vary in a few bases) and is hence recognized and excised by Flippase (Flp). There is a terminator upstream of the second F3 site and a RFP gene is immediately downstream. So in the absence of Flp RFP is not expressed, But when Flp excises the region between the F3 sites, RFP is expressed.

Figure:3


Figure:4


The PvuII digest was as shown below. From this the band of size 1549 bp was isolated from the gel and purified.

F3-ZeoR-F3-RFP digest with PvuII.JPG

Both pTetFlp KanR and F3-ZeoR-F3-RFP fragments were linear, so linear+linear Red/ET was done. The digets of 13 mini preps were as follows.

PTetFlp-KanR+F3-ZeoR-F3-RFP, digested with PstI.JPG

3 correct clones were re-electroporated and transformed. 23 minis were done from this. This is shown below.

Re-electroporated pTetFlp-KanR+F3-ZeoR-F3-RFP, digested with PstI.JPG



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