Furukawa K, Roth S
Biochem J. 1985 Apr 15;227(2):573-82. doi: 10.1042/bj2270573.
Two galactosyltransferases with nearly identical Mr values were purified 5000-7000-fold from microsomal membranes of chick-embryo livers by using several affinity columns. One enzyme transfers galactose from UDP-galactose to form a beta-(1----4)-linkage to GlcNAc (N-acetylglucosamine) or AsAgAGP [asialo-agalacto-(alpha 1-acid glycoprotein)]. The other enzyme forms a beta-(1----3)-linkage to AsOSM [asialo-(ovine submaxillary mucin)]. Both enzymes were solubilized (85%) from a microsomal pellet by using 1% Triton X-100 in 0.1 M-NaCl. The supernatant activities were subjected to DEAE-Sepharose chromatography and four affinity columns: UDP-hexanolamine-Sepharose, alpha-lactalbumin-Sepharose, GlcNAc-Sepharose and either AsAgAGP-Sepharose or AsOSM-Sepharose. The AsAgAGP enzyme [(1----4)-transferase] and the AsOSM enzyme [(1----3)-transferase] behave identically on the DEAE-Sepharose and UDP-hexanolamine-Sepharose columns, and similarly on the alpha-lactalbumin-Sepharose column. Final separation of the two enzymes, however, could only be achieved on affinity columns of their immobilized respective acceptors. Both purified enzymes migrate as a single band on sodium dodecyl sulphate/polyacrylamide-gel electrophoresis after silver staining, and both have an apparent Mr of 68 000. The enzymes were radioiodinated and again subjected to sodium dodecyl sulphate/polyacrylamide-gel electrophoresis. Radioautographic analyses showed only one, intensely radioactive, band. Activity stains performed for both transferases after cellulose acetate electrophoresis indicate that, with this system too, both activities have identical mobilities, and co-migrate, as well, with the major, silver-stained, protein band. Kinetic studies with the purified enzymes show that the Km value for GlcNAc, for the (1----4)-transferase, is 4mM; for the (1----3)-transferase the Km value for AsOSM is 5mM, in terms of GalNAc (N-acetylgalactosamine) equivalents. Both enzymes have a Km value of 25 microM for UDP-galactose.
利用几种亲和柱从鸡胚肝脏微粒体膜中纯化出两种相对分子质量几乎相同的半乳糖基转移酶,纯化倍数达5000 - 7000倍。一种酶将UDP - 半乳糖中的半乳糖转移,形成与GlcNAc(N - 乙酰葡糖胺)或AsAgAGP[去唾液酸 - 去半乳糖 -(α1 - 酸性糖蛋白)]的β-(1→4)连接。另一种酶则形成与AsOSM[去唾液酸 -(羊下颌粘蛋白)]的β-(1→3)连接。两种酶都用含1% Triton X - 100的0.1M - NaCl溶液从微粒体沉淀中增溶(85%)。将上清液活性物质进行DEAE - 琼脂糖凝胶柱层析,并通过四个亲和柱:UDP - 己醇胺 - 琼脂糖柱、α - 乳白蛋白 - 琼脂糖柱、GlcNAc - 琼脂糖柱以及AsAgAGP - 琼脂糖柱或AsOSM - 琼脂糖柱。AsAgAGP酶[(1→4)转移酶]和AsOSM酶[(1→3)转移酶]在DEAE - 琼脂糖柱和UDP - 己醇胺 - 琼脂糖柱上表现相同,在α - 乳白蛋白 - 琼脂糖柱上也类似。然而,两种酶的最终分离只能在其各自固定化受体的亲和柱上实现。两种纯化后的酶在银染后的十二烷基硫酸钠/聚丙烯酰胺凝胶电泳中均迁移为单一谱带,且表观相对分子质量均为68000。对酶进行放射性碘化后再次进行十二烷基硫酸钠/聚丙烯酰胺凝胶电泳。放射自显影分析仅显示一条强放射性谱带。在醋酸纤维素电泳后对两种转移酶进行活性染色表明,在该系统中,两种活性也具有相同的迁移率,并且与主要的银染蛋白带共同迁移。对纯化酶的动力学研究表明,对于(1→4)转移酶,GlcNAc的Km值为4mM;对于(1→3)转移酶,以GalNAc(N - 乙酰半乳糖胺)当量计,AsOSM的Km值为5mM。两种酶对UDP - 半乳糖的Km值均为25μM。