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. 2014 Feb;196(4):811–824. doi: 10.1128/JB.01104-13

TABLE 2.

Frequency of recombination of S. meliloti megaplasmid deletions into wild-type strains carrying the empty plasmid vector pTH1931 or pTH1931 containing TA genesa

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a

The diagram above the table illustrates the two homologous recombination events (dashed lines) that occur in transduction of deletion ΔCDET::Gmr Nmr from a donor strain into a wild-type recipient. The structure of the resulting Gmr Nmr transductant (recombinant) is shown. Similarly, the Gmr Nmr-marked ΔA257, ΔA131, ΔA132, and ΔB139 deletions (Fig. 2 and 3) were transduced using phage ΦM12 into RmP110 wild-type (WT) recipient strains carrying the empty Spr plasmid vector pTH1931 or pTH1931 carrying the TA gene regions as indicated.

b

Numbers of transductant colonies per plate as well as transductional frequency per recipient for each transduction are indicated. Results are representative of three independent experiments.