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. 2001 Jan;183(2):580–586. doi: 10.1128/JB.183.2.580-586.2001

TABLE 2.

Regulation of β-galactosidase expression directed by the vegII promoter and cre-containing vegII promoter derivatives in S. xylosus wild-type and mutant strains altered in catabolite repression

cre operatora Strain Genotypeb β-Galactosidase activity (nmol of nitrophenol produced/ min/mg of protein)c
B medium B medium + glucose Glucose repression ratiod
None TX302 Wild type 139 150 0.9
TX602 ccpA::ermB 125 131 0.9
TX402 ΔglkA 120 127 0.9
TX502 ΔglcU 110 122 0.9
TX702 hprK::ermB 124 97 1.3
malRA TX313 Wild type 82 26 3.2
TX613 ccpA::ermB 97 90 1.1
TX413 ΔglkA 89 53 1.7
TX513 ΔglcU 87 42 2.1
TX713 hprK::ermB 81 70 1.1
xylAB TX314 Wild type 38 5 7.6
TX614 ccpA::ermB 68 62 1.1
TX414 ΔglkA 33 9 3.7
TX514 ΔglcU 36 11 3.2
TX714 hprK::ermB 55 47 1.2
ccpA TX315 Wild type 104 25 4.1
TX615 ccpA::ermB 114 110 1.0
TX415 ΔglkA 110 57 1.9
TX515 ΔglcU 106 55 1.9
TX715 hprK::ermB 98 91 1.1
lacPH TX316 Wild type 38 16 2.4
TX616 ccpA::ermB 51 53 1.0
TX416 ΔglkA 36 24 1.5
TX516 ΔglcU 38 25 1.5
TX716 hprK::ermB 56 50 1.1
scrA TX320 Wild type 128 71 1.8
TX620 ccpA::ermB 118 115 1.0
TX420 ΔglkA 124 116 1.1
TX520 ΔglcU 108 94 1.2
TX720 hprK::ermB 103 91 1.2
a

The sequences of the integrated cre operators are listed in Fig. 2; cre sequences were designated according to their corresponding genes. 

b

Only the genotype relevant for regulation is shown. In all strains, the lac region is modified (′lacR ΔlacP P-lacH). 

c

Mean values of three independent cultures are presented. The standard deviations did not exceed ±15%. Strains were grown in complex B medium to an OD578 of 1; 25 mM glucose was added as indicated. After 1 h of further growth, the OD578 was determined, and the cells were harvested and disrupted with glass beads. Extracts prepared from 30 ml of cells adjusted to an OD578 of 2 were used for the determination of β-galactosidase activities. 

d

The glucose repression ratio was calculated by dividing the enzyme activity found in cultures in B medium by the enzyme activity detected in glucose-containing cultures.