TABLE 1.
Influence of growth conditions on the expression of glucuronidase by P. cellulosa
Carbohydrate added to Luria-Bertani growth mediuma | Enzyme activityb
|
|
---|---|---|
α-Glucuronidasec | β-Glucuronidased | |
None | NDe | ND |
4-O-Methyl-d-glucuronoxylan | 45 ± 5 | 32 ± 4 |
Oat spelt xylan | 75 ± 6 | 60 ± 6 |
Wheat arabinoxylan | 32 ± 3 | 33 ± 7 |
Rye arabinoxylan | 51 ± 6 | 41 ± 7 |
Oat spelt xylan and glucose | ND | ND |
Glucuronic acid | ND | ND |
β-Glucan | ND | ND |
Carbohydrates were each added to a final concentration of 0.2%.
α-Glucuronidase and β-glucuronidase activities, expressed as nanomoles of product per minute per milligram of total bacterial protein, were measured when the cultures reached the mid-log phase. The substrates employed were aldobiouronic acid (2 mM) to measure α-glucuronidase activity and 4-methylumbelliferyl-β-glucuronide (1 mM) to measure β-glucuronidase activity, as described elsewhere (7).
α-Glucuronidase activity was determined in cultures of wild-type P. cellulosa.
β-Glucuronidase activity was determined in cultures of P. cellulosa harboring pTN5.
ND, no activity detected. The sensitivities of the assays were such that 100 pmol of product/min/mg of protein could be detected with the α-glucuronidase assay and 1 pmol of product/min/mg protein could be detect with the β-glucuronidase assay.