TABLE 2.
α-Glucosidase and amylase activities of whole-cell extracts of strainsa
Strain | Growth substrate (carbon source) | Activityb (U/g of cell protein)
|
|
---|---|---|---|
α-Glucosidase | Amylase | ||
BT5482 | Glucose | 2.2c | <0.6 |
Maltose | 60.3 | 49.1 | |
BTΩsusR | Glucose | <0.6 | <0.6 |
Maltose | 7.4 | <0.6 | |
BTΩsusB | Glucose | ND | ND |
Maltose | 6.1 | 84.9 | |
BTΩsusRΩmalR | Glucose | <0.6 | <0.6 |
Maltose | 1.5 | <0.6 | |
BTΩmalR | Glucose | <0.6 | <0.6 |
Maltose | 14.0 | 5.7 | |
BTΩsusBΩmalR | Glucose | ND | ND |
Maltose | <0.6 | 4.5 |
For this assay, strains were grown on minimal medium containing glucose or maltose (0.3%).
The substrates used to detect α-glucosidase and amylase activities are p-nitrophenyl-α-d-glucopyranoside and 4-nitrophenyl-α-d-maltoheptaoside-4,6-O-ethylidene, respectively. One unit of activity was defined as one micromole of p-nitrophenol liberated per minute. This experiment was conducted in duplicate, and the variation between replicates was <10%. ND, not determined.
There was some α-glucosidase activity from wild type on glucose, so there was a basal level expression of α-glucosidase on glucose.