1985
DOI: 10.3136/nskkk1962.32.8_582
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High-pressure liquid chromatographic determination of naringinase activity.

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“…and the activity ofthe enzyme was assayed using soluble starch as the substrate by measuring the decrease in iodine-staining power as previously described (Kometani et al, 1994b), p-Amylase from sweet potato was from the Sigma Chemical Co., Ltd. and one unit of the enzyme was defined as the amount of enzyme that formed I mg of maltose from starch in 3 min at 20'C and pH 4.8. Naringinase(commercial enzyme mixture of a-rhamnosidase and ~-glucosidase from Aspergillus niger) was a gift from the Tanabe Seiyaku Co., Ltd. a-Rhamnosidase activity was assayed according to a previously described method (Horiuchi et al, 1985) with slight modification ofthe HPLC conditions. The activity was assayed using naringin as a substrate by measuring the decrease in the amount of substrate with HPLC on an ODS as will be described later.…”
Section: Methodsmentioning
confidence: 99%
“…and the activity ofthe enzyme was assayed using soluble starch as the substrate by measuring the decrease in iodine-staining power as previously described (Kometani et al, 1994b), p-Amylase from sweet potato was from the Sigma Chemical Co., Ltd. and one unit of the enzyme was defined as the amount of enzyme that formed I mg of maltose from starch in 3 min at 20'C and pH 4.8. Naringinase(commercial enzyme mixture of a-rhamnosidase and ~-glucosidase from Aspergillus niger) was a gift from the Tanabe Seiyaku Co., Ltd. a-Rhamnosidase activity was assayed according to a previously described method (Horiuchi et al, 1985) with slight modification ofthe HPLC conditions. The activity was assayed using naringin as a substrate by measuring the decrease in the amount of substrate with HPLC on an ODS as will be described later.…”
Section: Methodsmentioning
confidence: 99%