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. 2010 Oct 1;192(23):6182–6190. doi: 10.1128/JB.00176-10

TABLE 4.

Effect of iteron number on coresident plasmid segregation patterns in the absence and presence of excess RepC

pRAS1 plasmid Coresident plasmidsa
% colonies with resistance to the following antibiotic(s):
Direction and strength of segregation biasb
pRAS3.1.35.Km + pBAD28 pRAS3.1.35.Km + pBAD28-RepC Tet only Km only Tet and Km
pRAS3.1.35.Tet 53 ± 11 21 ± 6 28 ± 10 Tet > Km
55 ± 8 17 ± 1 29 ± 5 Tet > Km
pRAS3.1 91 ± 6 1 ± 1 7 ± 5 4 iterons >>> 3 iterons
88 ± 4 7 ± 3 6 ± 0 4 iterons >>> 3 iterons
pRAS3.1.55.Tet 79 ± 3 6 ± 3 14 ± 6 5 iterons ≫ 3 iterons
67 ± 2 16 ± 2 21 ± 1 5 iterons ≫ 3 iterons
pRAS3.1.75.Tet 63 ± 14 25 ± 13 15 ± 2 7 iterons > 3 iterons
63 ± 11 26 ± 13 13 ± 4 7 iterons > 3 iterons
a

The small black circles indicate the two plasmids in the cell in addition to the pRAS3 plasmid used in each experiment. All plasmids were completely stable in the absence of antibiotics for the duration of the assay.

b

Direction and strength of segregation bias as a result of iteron number in the absence or presence of additional RepC. Arrowheads indicate the direction of plasmid displacement, and the number of arrowheads is an indication of the strength of displacement.