pRE112, pRE107, pRE118, pDMS197, pGP704 Plasmid

等位交換載體，自殺質粒

BioVector NTCC質粒載體菌種細胞蛋白抗體基因保藏中心

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 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.

Map圖譜：

BioVector NTCC質粒載體菌種細胞蛋白抗體基因保藏中心