Structures of four-way junctions in gene <i>17</i> of T3 and T7.

<p>(A) T3 nt 33324–33353 (B) T3 nt 33317–33347 (C) T7 nt 35109–35139 (D) T7 nt 35082–35117. One strand is highlighted in grey; the other is not. Arrows indicate Endo I cutting sites.</p

Efficiency of plating of phages on <i>E. coli</i> female and male strains determined at 37°C.

<p>Efficiency of plating of phages on <i>E. coli</i> female and male strains determined at 37°C.</p

Alignment of T3 and T7 sequences near the crossover regions seen in the T3/7 phage.

<p>(A) Within gene <i>17</i>. (B) Within gene <i>18.5</i>. Sequences were aligned by ClustalW. The parent phages of the two sides of the crossover region (shown by arrows) are indicated on top of the alignment.</p

The mechanism of endonucleolytic cleavages at nonequivalent sites and strand annealing (CNSA).

<p>Colors and arrows are the same as those of <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0030954#pone-0030954-g005" target="_blank">Figure 5</a>. The steps are: 1, production of DSBs by cutting at nonequivalent sites of T3 and T7 DNA; 2, 5′ resections of DSBs of T3 and T7; 3, annealing of the T3 DSBs with the T7 DSB; 4, removal of the nonhomologous nucleotides, filling the gap, and ligation.</p

Structures of four-way junctions in gene <i>18.5</i> of T3 and T7.

<p>(A) T3 nt 35315–35345 or equivalently T7 nt 37094–37124 (B) T7 nt 37163–37188. One of the strands is highlighted in grey. Endo I cutting sites are shown by arrows.</p

Adsorption efficiency (%) of phages on <i>E. coli</i> female and male strains.

<p>Adsorption efficiency (%) of phages on <i>E. coli</i> female and male strains.</p