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A portable attTn7 target site

Single-target transposition to the bacterial genome is dependent on the presence of a conserved sequence, encompasing the 3' end of the glmS gene, encoding glucosamine synthetase, and part the intergenic region immediately downstream, designated the attTn7 site. This region is highly conserved (Milewski, 2002), and Tn7 transposition has been demonstrated in over 20 bacterial species (Craig, 1996). However, the lack of a suitable target may be the limiting factor in some of the organisms in which Tn7 transposition does not occur, including a variety of bacteria, but also archea and eukaryotes. The possibility of inserting a functional attTn7 in the genomes of these organisms may enable site-specific Tn7 transposition for at least some of them, thus expanding the host range of this transposon and its derived tools, such as the miniTn7 BioBrick toolkit.

Construction of a "portable" attTn7

As a first step toward this goal, we undertook the cloning of the functional E. coli attTn7 (BBa_K510022) into a plasmid vector, and the demonstration that this "portable" plasmid-borne attTn7 can be recognized as a Tn7 transposition target by our miniTn7BB minitransposons. The attTn7 was PCR-amplified from the chromosome of the E. coli K12 strain MC4100 with primers bearing prefix and suffix restriction sites, cleaved and ligated into pSB1C3. The construct was verified by sequencing.

Characterization of the "portable" attTn7

For preliminary characterization of the "portable" attTn7, we attempted to demonstrate transposition into the plasmid-borne target. The miniTn7BB-Gm transposon was transferred into E. coli DH5α bearing pSB1C3-attTn7 by tetraparental mating using the helper plasmid pTNS2to provide the Tn7 transposition functions. Transconjugants bearing transposon insertions were selected on LB plates supplemented with gentamycin and chloramphenicol. To identify clones bearing the transposon insertion at the plasmid-borne target, transconjugant colonies were pooled, plasmid DNA was extracted from the pool and used to transform E. coli. Transformants were selected on LB plates containing chloramphenicol and scored for gentamycin resistance (Figure 1). 97 out of 100 colonies had become simultaneously resistant to both antibiotics, strongly suggesting that the miniTn7BB-Gm was inserted in the chloramphenicol resistance plasmid, and transferred along with its target. Restriction analysis confirmed that indeed this was the case, and that the transposon was inserted within the att-Tn7 target site at the pSB1C3-attTn7 plasmid (data not shown).

Figure 1. Patches of E. coli transformed with plasmid DNA from pooled colonies obtained after insertion of pUC18Sfi-miniTn7BB-Gm into the genome of E.coli DH5α bearing pSC1C3-attTn7. Open squares indicate patches showing sensitivity to gentamycin , that is, not bearing the miniTn7 transposon insertion.

Construction of a miniTn7 transposon bearing the "portable" attTn7

This module allows the integration of BioBricks into bacterial chromosomes (using prefix or suffix restriction sites that flank the attTn7), while regenerating an intact Tn7 attachment site for further genetic manipulation. Thus, the miniTn7BB-Gm-attTn7 allow further integration of BioBrick parts in the chromosome of a strain that already has a copy of mimni Tn7 inserted.