An extracellular naringinase (an enzyme complex consisting of a-L-rhamnosidase and b-D-glucosidase activity, EC 3.2.1.40) that hydrolyses naringin (a trihydroxy flavonoid) for the production of rhamnose and glucose was purified from the culture filtrate of Aspergillus niger 1344. The enzyme was purified 38-fold by ammonium sulphate precipitation, ion exchange and gel filtration chromatography with an overall recovery of 19% with a specific activity of 867 units per mg of protein. The molecular mass of the purified enzyme was estimated to be about 168 kDa by gel filtration chromatography on a Sephadex G-200 column and the molecular mass of the subunits was estimated to be 85 kDa by sodium dodecyl sulphate-Polyacrylamide gel electrophoresis (SDS-PAGE). The enzyme had an optimum pH of 4.0 and temperature of 50°C, respectively. The naringinase was stable at 37°C for 72 h, whereas at 40°C the enzyme showed 50% inactivation after 96 h of incubation. Hg 2+ , SDS, p-chloromercuribenzoate, Cu 2+ and Mn 2+ completely inhibited the enzyme activity at a concentration of 2.5-10 mM, whereas, Ca 2+ , Co 2+ and Mg 2+ showed very little inactivation even at high concentrations (10-100 mM). The enzyme activity was strongly inhibited by rhamnose, the end product of naringin hydrolysis. The enzyme activity was accelerated by Mg 2+ and remained stable for one year after storage at )20°C. The purified enzyme preparation successfully hydrolysed naringin and rutin, but not hesperidin.