Takagaki K, Kon A, Kawasaki H, Nakamura T, Endo M
Department of Biochemistry, Hirosaki University School of Medicine, Japan.
J Biochem Biophys Methods. 1989 Aug-Sep;19(2-3):207-14. doi: 10.1016/0165-022x(89)90027-4.
The present paper describes a fluorometric assay for galactosaminoglycan-degrading endo-beta-xylosidase, utilizing glycosaminoglycan chains bearing a 4-methylumbelliferyl group at the reducing terminus as a substrate. This fluorogenic substrate is synthesized by human skin fibroblasts cultured in the presence of a fluorogenic xyloside, 4-methylumbelliferyl-beta-D-xyloside. The assay is based on measurement of the fluorescence of 4-methylumbelliferone, enzymatically liberated from the synthetic substrate by endo-beta-xylosidase. We examined the applicability of the assay for analysis of endo-beta-xylosidase activity.