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Enzyme α-L-rhamnosidase

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  • An alkali tolerant α-L-rhamnosidase from the culture filtrate of a fungal strain, Fusarium poae MTCC-2086 has been purified to homogeneity. The procedure involved concentration by ultrafiltration and cation-exchange chromatography on carboxymethyl cellulose. The purified enzyme gave a single protein band corresponding to molecular mass of 51.0 kDa in SDS-PAGE analysis showing that the enzyme preparation was pure. The native PAGE analysis of the purified enzyme also gave single protein band confirming the purity of the enzyme preparation.

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