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 | |
The sequences of the integrated cre operators are listed in Fig. 2; cre sequences were designated according to their corresponding genes.
Only the genotype relevant for regulation is shown. In all strains, the lac region is modified (′lacR ΔlacP P-lacH).
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.
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.