TABLE 3.
Mutational analysis of the his leader regiona
| Plasmid | Potential mRNA structure present upstream of lux AB genesb | Luciferase activities (lx/OD [103])
|
Strength of termination (fold)c | Antitermination factor (fold)d | |
|---|---|---|---|---|---|
| CDM+H | CDM−H | ||||
| pJIM2530 | ![]() |
960 ± 190 | 930 ± 160 | 1 | 1 |
| pTer-4 | 23 ± 4 | 330 ± 40 | 42 | 14 | |
| pTer-3 | 10 ± 2 | 17 ± 0.6 | 96 | 1.7 | |
| pTer-2 | 5.2 ± 0.4 | 6.9 ± 0.3 | 185 | 1.3 | |
| pTer-4m1 | 10 ± 2 | 19 ± 3 | 96 | 1.9 | |
| pTer-4m2 | 12 ± 2 | 19 ± 3 | 80 | 1.6 | |
To study attenuation mechanism, the luciferase activity resulting from the insertion of various derivatives of the DNA segment carrying the his leader region between a constitutive promoter (PorfD-repE) and the lux genes on a plasmid was measured in L. lactis growing in CDM with or without histidine.
Fusions are under the control of constitutive promoter PorfD-repE from pJIM2530.
Quotient of the lux value of the control plasmid pJIM2530 and that of the indicated plasmid in the presence of histidine.
Quotient of the lux value obtained in the absence of histidine and that obtained in the presence of histidine for the same plasmid.
