Thompson D B, Daniel W L, Glaser J H
Comp Biochem Physiol B. 1985;82(1):55-61. doi: 10.1016/0305-0491(85)90127-0.
Approximately 25 and 40%, respectively, of murine (Mus musculus) and rat (Rattus norvegicus) hepatic arylsulfatase (EC 3.1.6.1) activity eluted from DEAE-ion exchange resins under high salt conditions. This high salt fraction contained arylsulfatase A and an enzyme which was immunologically similar to arylsulfatase B. The latter enzyme was thermostable, resistant to inhibition by silver, completely inhibited by phosphate, displayed linear kinetics, and had a higher pH optimum than arylsulfatase A. Anionic arylsulfatase B also hydrolyzed chondroitin-4-SO4 heptasaccharide. Sephacryl S-300 gel filtration resolved anionic arylsulfatase B into 55 and 115 kd fractions. Rodent arylsulfatase A activity was grossly underestimated when 4-methyl-umbelliferyl sulfate was employed as substrate.
在高盐条件下,分别约有25%和40%的小鼠(小家鼠)和大鼠(褐家鼠)肝脏芳基硫酸酯酶(EC 3.1.6.1)活性从DEAE离子交换树脂上洗脱下来。这个高盐组分包含芳基硫酸酯酶A和一种在免疫学上与芳基硫酸酯酶B相似的酶。后一种酶耐热,对银抑制有抗性,被磷酸盐完全抑制,呈现线性动力学,并且比芳基硫酸酯酶A有更高的最适pH值。阴离子型芳基硫酸酯酶B也能水解硫酸软骨素-4-硫酸七糖。Sephacryl S-300凝胶过滤将阴离子型芳基硫酸酯酶B分离成55和115 kd的组分。当使用4-甲基伞形酮基硫酸酯作为底物时,啮齿动物芳基硫酸酯酶A的活性被严重低估。