“…Naringin (4′,-5,7′-trihydroxyflavonone-7-rhamnoglucoside) is first hydrolyzed by α-L-rhamnosidase activity of naringinase to rhamnose and prunin (one third of the bitterness of naringin) which can be further hydrolyzed into glucose and naringenin by the β-D-glucosidase component of naringinase. The potential application of rhamnosidase is used in the debittering of citrus fruit juices (Busto et al, 2007), manufacture of prunin from naringin, manufacture of L-rhamnose by hydrolysis of natural glycosides containing terminal L-rhamnose, enhancement of wine aromas by enzymatic hydrolysis of terpenyl glycosides containing L-rhamnose, elimination of hesperidin crystals from orange juices, conversion of chloropolysporin B to chloropolysporin C, the derhamnosylation of many L-rhamnose containing steroids for example, diosgene, desglucoruscin, ginsenosides-Rg2, etc. whose derhamnosylated products have their clinical importance (Feng et al, 2005).…”