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. 2001 Oct;183(19):5675–5683. doi: 10.1128/JB.183.19.5675-5683.2001

TABLE 2.

Repression of the maltose regulon when glp genes are amplified

Fusion and introduced plasmida β-Galactosidase activityb
Repression by glpc
pHo 5 pHo 7 pHo 5 pHo 7
Φ(malK′-lacZ+)1 (pGPH1768)
 pACYC177 189 ± 11 339 ± 51
 pGPH9925 (glpFKX) VL VL Full Full
 pGPH11250 (glpFK) VL VL Full Full
 pGPH9993 (glpF) 136 ± 18 328 ± 29 1.4 1
 pGPH11264 (glpK) VL 90 ± 32 Full 3.8
 pGPH11249 (glpX) 153 ± 40 295 ± 74 1.2 1.1
Φ(malT′-lacZ+)1 (pGPH8881)
 pACYC177 417 ± 86 593 ± 41
 pGPH9925 (glpFKX) 162 ± 35 194 ± 25 2.6 3.1
 pGPH11250 (glpFK) 150 ± 21 244 ± 58 2.8 2.4
 pGPH9993 (glpF) 328 ± 7 657 ± 53 1.3 1.1
 pGPH11264 (glpK) 128 ± 37 232 ± 34 3.3 2.6
 pGPH11249 (glpX) 395 ± 58 656 ± 93 1.1 0.9
Φ(malP′-lacZ+)1 (pGPH9463)
 pACYC177 1,261 ± 21 2,321 ± 163
 pGPH9925 (glpFKX) ND 1,116 ± 26 2.1
a

Fusions were in an MC4100 background in pJEL250. 

b

β-Galactosidase activity was assayed during growth at 30°C in MM adjusted to pH 5 or 7 and supplemented with glycerol [and maltose for Φ(malP′-lacZ+)1], ampicillin, and kanamycin. ND, not done; VL, very low β-galactosidase activity (below the sensitivity threshold of the method used). 

c

Repression values correspond to the ratio between β-galactosidase activities of the strain with pACYC177 and the strain with amplified glp genes.