Biochemical Journal 1988-09-15

One-proton catalysis by the alpha-L-arabinofuranosidase III of Monilinia fructigena.

T Selwood, M L Sinnott

Index: Biochem. J. 254 , 899, (1988)

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Abstract

1. Michaelis-Menten parameters for the hydrolysis of p-nitrophenyl alpha-L-arabinofuranoside were measured as a function of pL (pH or pD) in both 1H2O and 2H2O. 2. The variation of both Vmax. and Vmax./Km with pL is sigmoid, the pK governing Vmax. shifting from 6.34 +/- 0.05 in 1H2O to 6.84 +/- 0.07 in 2H2O, and that governing Vmax./Km from 5.89 +/- 0.03 in 1H2O to 6.38 +/- 0.05 in 2H2O. 3. In the plateau regions there is a small inverse solvent isotope effect on Vmax./Km (0.92), and one of 1.45 on Vmax. 4. The variation of Vmax. with isotopic composition is strictly linear, indicating that the isotope effect arises from the transfer of a single proton.

Related Compounds

Structure Name/CAS No. Articles
4-NITROPHENYL A-L-ARABINOFURANOSIDE Structure 4-NITROPHENYL A-L-ARABINOFURANOSIDE
CAS:6892-58-6