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. 2013 Feb 6;5(2):619–653. doi: 10.3390/v5020619

Table 6.

Influence of modifying P or dnaB on P lethality and plasmid loss.

Host cells and plasmids Cell viability a and (plasmid retention/cfu; %) b at growth temperature (˚C)
25 Ave 37 & 39 42
594[pcIpR- P-timm] 1.0 0.0049 0.001
(195/196; ~100) (0/57; 0) (0/28; 0)
594[pcIpR- PSPA-timm] 1.0 0.006 0.004
(14/14; 100) (0/150; 0) (0/39; 0)
594[pcIpR- Pπ-timm] 1.0 0.635 0.003
(103/103; 100) (789/793; ~100) (0/294; 0)
594[pcIpR- PΔ76-timm] 1.0 0.96 0.12
(166/168; 99) (334/336; 99) (166/168; 99)
594 grpD55 [pcIpR-P-timm] 1.0 0.99 1.0
(35/35; 100) (87/88; 99) (14/14; 100)
594 grpD55 [pcIpR-PSPA-timm] 1.0 0.75 0.57
(42/42; 100) (88/94; 94) (18/19; 95)
594 grpD55 [pcIpR-Pπ-timm] 1.0 0.08 0.01
(54/54; 100) (434/435; ~100) (5/108; 5)
594 grpD55 [pcIpR-PΔ76-timm] 1.0 (nd) 0.45 (nd) 0.001 (nd)
Re-claim pcIpR-P-timm from 594 grpD55 cultures and transform into 594 dnaB+ cells
Re-claim from 25˚C cultures c 1.0 0.08 0.01
(54/56; 96) (0/119; 0) (0/91; 0)
Re-claim from 42˚C cultures d 1.0 0.059 0.026
(130/130; 96) (1/230; 0.4) (0/201; 0)

a : The cell viability shown in each column entry, in top line, was determined by dividing the cell titer obtained at each given incubation temperature by the cell titer at 25 ˚C.) Refer to Experimental Section 3.5.

b: The values in parentheses in each column entry show the number of AmpR cfu / number of survivor cfu assayed per indicated temperature; the value following represents the percentage of AmpR cfu with plasmids, and was rounded up. All data show the results for two or more independently transformed single colonies.

c : Exp.’s for sc1, sc2.

d : Exp.’s for sc’s 3,4,5, 6.