Sarkar M
Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.
Glycoconj J. 1994 Jun;11(3):204-9. doi: 10.1007/BF00731219.
UDP-GlcNAc: alpha 3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GnT I; EC 2.4.1.101) catalyses a key reaction in the conversion of oligomannose to complex and hybrid N-glycans. The cytoplasmic tail and transmembrane segment of rabbit GnT I cDNA were replaced with an in-frame cleavable signal sequence and the hybrid construct was inserted into the genome of Autographa californica nuclear polyhedrosis virus (AcMNPV) under the control of the polyhedrin promoter. Sf9 insect cells were infected with the recombinant baculovirus and the enzymatically active and soluble catalytic domain of GnT I was purified from the medium (1-5 mg l-1) in two steps to a specific activity of about 2 mumol min-1 mg-1 protein. Recombinant GnT I has been used for the chemical-enzymatic synthesis of analogues of Man alpha 1-6]GlcNAc beta 1-2Man alpha 1-3]Man beta-O-octyl.
UDP-N-乙酰葡糖胺:α3-D-甘露糖苷β-1,2-N-乙酰葡糖胺基转移酶I(GnT I;EC 2.4.1.101)催化寡甘露糖向复杂型和杂合型N-聚糖转化过程中的关键反应。将兔GnT I cDNA的胞质尾段和跨膜区段替换为框内可切割信号序列,并将该杂合构建体在多角体蛋白启动子的控制下插入苜蓿银纹夜蛾核型多角体病毒(AcMNPV)的基因组中。用重组杆状病毒感染Sf9昆虫细胞,然后分两步从培养基(1 - 5 mg l-1)中纯化出具有酶活性且可溶的GnT I催化结构域,其比活性约为2 μmol min-1 mg-1蛋白质。重组GnT I已用于[Manα1-6]GlcNAcβ1-2Manα1-3]Manβ-O-辛酯类似物的化学酶促合成。