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. 2002 Oct;68(10):5034–5041. doi: 10.1128/AEM.68.10.5034-5041.2002

TABLE 3.

Comparison of β-galactosidase activities and stabilities of the heterologous genes from the cascade and single expression systems in different configurations

Strain Plasmid β-Galactosidase activity (Miller units)a
β-Galactosidase/total proteins (%)b
% of Lac+ coloniesc
−2OHB +2OHB −2OHB +2OHB −2OHB +2OHB
CC118λpir pTPm-lacZ 1,211 1,358 NDd ND 100 100
CC118λpir pCNB2-lacZ 10,917 67,002 3.6 13 98, 81 20, 1.5
CC118λpir pCNB4-lacZ 510 17,952 ND 3.9 100, 97 96, 85
CC4S2PT32 171 30,383 ND 8.8 100 100
CC4S2PT97 408 39,143 ND 11 100 100
CC1184S2λpir pTPm-lacZ 1,487 78,257 ND 20 100, 99 5, 0
a

β-Galactosidase activity was assayed after 5 h of incubation without salicylate (−2OHB) or with 2 mM salicylate (+2OHB). The data are means from three independent experiments.

b

The relative amounts of β-galactosidase in cells were measured by densitometry of Coomassie blue-stained SDS-8% PAGE gels.

c

The stability assay was performed as described in Materials and Methods. Three independent experiments were performed for each strain and type of conditions. As expected, the values varied considerably for the experiments with the plasmid-containing strains, probably due to the stochastic appearance of the cured strains during culture. The maximum and minimum values are shown except for cases when identical results were obtained.

d

ND, not determined (0.5%).