pRE112
(Plasmid #43828)

• Purpose: (Empty Backbone)
• Depositing Lab: Dieter Schifferli
• Publication: Edwards et al Gene. 1998 Jan 30;207(2):149-57.

Backbone

• Vector backbone: pRE107 (modified from pGP704)
• Backbone manufacturer: Addgene plasmid 43829
• Backbone size (bp): 5173
• Modifications to backbone: From pGP704: SacB1 from pUC58-sacB1 cloned into the EcoRI site. BamHI site in oriV converted to a ClaI site by partial digestion and Klenow treatment. From pRE107: Ampicillin resistance replaced with Chloramphenicol resistance (from pACYC184) by blunted-BamHI digestion.
• Vector type: Bacterial Expression ; Bacterial allelic exchange vector with sacB1
• Selectable markers: SacB (sucrose sensitivity)

Growth in Bacteria

• Bacterial Resistance(s): Chloramphenicol, 25 μg/mL
• Growth Temperature: 37°C
• Growth Strain(s): SM10 λpir
• Growth instructions: Contains lambda pir-dependent R6K replication origin; requires lambda pir-containing bacteria strain
• Copy number: Low Copy

Cloning Information

• Cloning method: Restriction Enzyme
• 5′ sequencing primer: CAT-F

Resource Information

• Supplemental Documents:
  • pRE112 annotated Genbank file
• A portion of this plasmid was derived from a plasmid made by: SM10 λpir bacterial strain and pGP704 plasmid backbone from John Mekalanos, Harvard Medical School, Boston, MA. SacB1 gene from plasmid pUC58-sacBI from Dennis Ohman, VCU Medical Center, Richmond, VA. CmR gene from pACYC184 (standard cloning vector - commercially available)
• Articles Citing this Plasmid:
  • 3 References

Terms and Licenses

• Academic/Nonprofit Terms:
  • UBMTA
• Industry Terms:
  • Not Available to Industry

Depositor Comments

The plasmids deposited here comprise a set of SacB1-dependent allelic exchange vectors improved from a previously described suicide vector, pGP704 (Miller and Mekalanos, 1988), by including a system to select for plasmid loss by recombination.

Plasmid pRE107 (Addgene plasmid #43829) was constructed by cloning the appropriate EcoRI fragment from pUC58-sacB1 (McIver et al., 1995) into pGP704 (see associated schematic image). The sacB1 allele is a modified variation of sacB, where unique restriction sites were removed by site directed mutagenesis (McIver et al., 1995). Additionally, the BamHI site in the R6K ori of the resulting plasmid was removed by partial BamHI digestion, blunting the resulting overhangs with PolIk (resulting in the formation of a ClaI site) and screening for its loss by restriction analysis.

To use this plasmid with bla fusions and increase the functionality of this system, the depositing laboratory replaced the ApR gene as follows.

The ApR gene flanked by the remaining BamHI sites was removed and replaced with either CmR, TcR or KmR resistance markers (see associated schematic image).

The CmR gene was PCR-amplified from pACYC184 using two primers

5′-CATGGTACCCGGGCCCTAAATACCTGTGACGGAAGAT-3′
and
5′-AACTGCAGACCCGGGCCCTATCACTTATTCAGGCGTAGC-3′

and standard conditions to produce a 958-bp fragment with overlapping SmaI/ApaI sites. This fragment was cloned into the blunted BamHI sites to produce plasmid pRE112.

The resulting plasmid together with others in this deposited series contain the conditional R6K ori, the origin of transfer (oriT) which allows conjugative transfer from permissive hosts, the sacB1 gene to provide negative selection and a MCS, along with a range of different AbR markers.