Sasaki T, Sukegawa K, Masue M, Fukuda S, Tomatsu S, Orii T
Department of Pediatrics, Gifu University School of Medicine.
J Biochem. 1991 Nov;110(5):842-6. doi: 10.1093/oxfordjournals.jbchem.a123668.
A deficiency in alpha-N-acetylglucosaminidase is known as mucopolysaccharidosis IIIB or Sanfilippo B syndrome. We purified this enzyme almost 39,000-fold from liver to homogeneity with 3% recovery. Use of concanavalin A (Con A)-Sepharose and heparin-Sepharose resulted in 13.4-fold and 11.6-fold purifications of the enzymatic activity, respectively. The molecular mass was estimated to be 300 kDa by gel filtration and 80 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis. The isoelectric point was 5.1, optimal pH was 4.5, and the Km for p-nitrophenyl alpha-N-acetylglucosamine was 0.13-0.20 mM. The purified enzyme was stable at 50 degrees C for 1 h and within the pH range of 6.5-8.5. Anti-serum against the purified enzyme raised in BALB/c mice inhibited the activities of alpha-N-acetylglucosaminidase.
α-N-乙酰氨基葡萄糖苷酶缺乏症被称为黏多糖贮积症IIIB型或桑菲利普B综合征。我们从肝脏中纯化该酶,纯化倍数近39000倍,达到同质,回收率为3%。使用伴刀豆球蛋白A(Con A)-琼脂糖和肝素-琼脂糖分别使酶活性纯化了13.4倍和11.6倍。通过凝胶过滤估计分子量为300 kDa,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分析估计为80 kDa。等电点为5.1,最适pH为4.5,对硝基苯基α-N-乙酰氨基葡萄糖的Km为0.13 - 0.20 mM。纯化后的酶在50℃下1小时稳定,在pH 6.5 - 8.5范围内稳定。在BALB/c小鼠中产生的针对纯化酶的抗血清抑制了α-N-乙酰氨基葡萄糖苷酶的活性。