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培养的大豆细胞可溶性酶制剂合成含甘露糖的脂连接寡糖。

Biosynthesis of mannose-containing lipid-linked oligosaccharides by solubilized enzyme preparation from cultured soybean cells.

机构信息

Department of Biochemistry, University of Texas Health Science Center, San Antonio, Texas 78284.

出版信息

Plant Physiol. 1985 Apr;77(4):840-6. doi: 10.1104/pp.77.4.840.

Abstract

Glycosyl transferases that participate in the assembly of the lipid-linked oligosaccharide intermediates were solubilized from cultured soybean cells using 0.3% Nonidet P-40 (NP-40) in the presence of 10% glycerol. The solubilized enzyme preparation was reasonably stable and 50% of the activity still remained after storage at -10 degrees C for 1 month. The solubilized enzyme synthesized [(14)C]Man(3)GlcNAc(2)-pyrophosphoryl-polyprenol and [(14)C]Man(5)GlcNAc(2)-pyrophosphoryl-polyprenol when incubated with GDP-[(14)C]mannose plus a partially purified acceptor lipid isolated from calf liver. The formation of these lipid-linked oligosaccharides did not require the addition of dolichyl-phosphate or metal ions. In fact, the addition of 5 to 10 millimolar ethylenediaminetetraacetate stimulated the incorporation of mannose into lipid-linked oligosaccharides 2- to 3-fold. Since little or no dolichyl-phosphoryl-mannose is formed in the presence of ethylenediaminetetraacetate, the results suggest that the mannosyl residues added to form Man(3)GlcNAc(2)-lipid and Man(5)GlcNAc(2)-lipid come directly from GDP-mannose without the participation of dolichyl-phosphoryl-mannose. On the other hand, the formation of significant amounts of Man(6)GlcNAc(2)-lipid, Man(7)GlcNAc(2)-lipid, and Man(8)GlcNAc(2)-lipid occurred when the above incubations were supplemented with dolichyl-phosphate and metal ions. Based on various time course studies and supplementation studies with various additions, it appears likely that the first five mannose residues to form Man(5)GlcNAc(2)-lipid come directly from GDP-mannose, whereas other mannose units to form larger oligosaccharide-lipids come from dolichyl-phosphoryl-mannose.

摘要

参与脂质连接寡糖中间体组装的糖基转移酶使用 0.3% NP-40(非离子型去污剂 NP-40)在 10%甘油存在下从培养的大豆细胞中溶解。该溶解酶制剂相当稳定,在-10°C 下储存 1 个月后,仍有 50%的活性保留。当用 GDP-[14C]甘露糖和从小牛肝脏中分离的部分纯化的受体脂质孵育时,溶解的酶合成[(14)C]Man(3)GlcNAc(2)-焦磷酸化多萜醇和[(14)C]Man(5)GlcNAc(2)-焦磷酸化多萜醇。这些脂质连接寡糖的形成不需要添加多萜醇磷酸或金属离子。事实上,添加 5 至 10 毫摩尔乙二胺四乙酸刺激甘露糖掺入脂质连接寡糖 2 至 3 倍。由于在乙二胺四乙酸存在下很少或根本不形成多萜醇磷酸甘露糖,结果表明,形成 Man(3)GlcNAc(2)-脂质和 Man(5)GlcNAc(2)-脂质的甘露糖残基直接来自 GDP-甘露糖,而不参与多萜醇磷酸甘露糖。另一方面,当上述孵育物补充多萜醇磷酸和金属离子时,会形成大量的 Man(6)GlcNAc(2)-脂质、Man(7)GlcNAc(2)-脂质和 Man(8)GlcNAc(2)-脂质。根据各种时间进程研究和各种添加物的补充研究,形成 Man(5)GlcNAc(2)-脂质的前五个甘露糖残基似乎直接来自 GDP-甘露糖,而形成较大寡糖脂质的其他甘露糖单位来自多萜醇磷酸甘露糖。

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