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The action of β-glucosidase on the methyl derivatives of  p -nitrophenyl β- d -glucopyranoside ( p NP-β-Glc), which were regio-specifically substituted at  O-2 ,  O-3 ,  O-4 , and  O-6  positions, was studied. Specifically, several β-glucosidases isolated from brown-rot, white-rot, soft-rot fungi, and almond were investigated. These β-glucosidases did not act on the 2, 3, and 4- O -methyl derivatives, while the 6- O -methyl one was hydrolyzed by all the enzymes to some extent. The results indicate that the methyl group at  O-2 ,  O-3 , and  O-4  of the glucopyranoside strongly inhibits the recognition by the β-glucopyranoside, while the enzymes do not discriminate the structure difference between  p NP-β-Glc and its methyl derivative at  O-6 .

Action of fungal β-glucosidase on the mono - O -methylated p -nitrophenyl β- d -glucopyranoside 2 nd ICC 2007, Tokyo, Japan, October 25–29, 2007