Shinoda K, Morishita Y, Sasaki K, Matsuda Y, Takahashi I, Nishi T
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., 3-6-6, Asahi-machi, Machida-shi, Tokyo 194, Japan.
J Biol Chem. 1997 Dec 19;272(51):31992-7. doi: 10.1074/jbc.272.51.31992.
The human alpha1,3-fucosyltransferase, Fuc-TVII, a key enzyme in the biosynthesis of selectin ligands, was expressed as a soluble protein-A chimeric form in a human B cell lymphoma cell line, Namalwa KJM-1, and purified using IgG-Sepharose. The enzymatic properties of recombinant soluble Fuc-TVII were then examined. Its enzyme activity was highest at pH 7.5, and the presence of 25 mM Mn2+ was required for full activity. Fuc-TVII exhibits an acceptor specificity restricted to alpha2,3-sialylated type 2 oligosaccharides, and the apparent Km values for alpha2,3-sialyl lacto-N-neotetraose and GDP-fucose were 3.08 mM and 16.4 microM, respectively. The inhibitory effects of various nucleotides on the activity of Fuc-TVII reflected its donor specificity for the nucleotide portion of GDP. Fuc-TVII was demonstrated to be useful for the synthesis of a sialyl Lewis x hexasaccharide from lacto-N-neotetraose in combination with an alpha2, 3-sialyltransferase, ST3Gal IV. Polyethylene glycols enhanced the thermal stability of Fuc-TVII, leading to increased formation of the reaction product.
人α1,3-岩藻糖基转移酶Fuc-TVII是选择素配体生物合成中的关键酶,它在人B细胞淋巴瘤细胞系Namalwa KJM-1中表达为可溶性蛋白A嵌合形式,并使用IgG-琼脂糖进行纯化。随后检测了重组可溶性Fuc-TVII的酶学性质。其酶活性在pH 7.5时最高,完全活性需要25 mM Mn2+的存在。Fuc-TVII表现出对α2,3-唾液酸化2型寡糖的受体特异性,α2,3-唾液酸乳糖-N-新四糖和GDP-岩藻糖的表观Km值分别为3.08 mM和16.4 μM。各种核苷酸对Fuc-TVII活性的抑制作用反映了其对GDP核苷酸部分的供体特异性。已证明Fuc-TVII与α2,3-唾液酸转移酶ST3Gal IV联合使用,可用于从乳糖-N-新四糖合成唾液酸化路易斯x六糖。聚乙二醇提高了Fuc-TVII的热稳定性,导致反应产物形成增加。