Goussault Y, Nakabayashi S, Warren C D, Bugge B, Jeanloz R W
Department of Biological Chemistry, Harvard Medical School, Boston, Massachusetts.
Carbohydr Res. 1988 Aug 15;179:381-92. doi: 10.1016/0008-6215(88)84134-x.
Incubation of calf pancreas microsomes with synthetic alpha-D-Manp-(1----6)-beta-D-Manp-(1----4)-beta-D-GlcpNAc-(1 ----4)-alpha-D- GlcpNAc-PP-Dol and GDP-D-[14C]-mannose gave three major lipid-linked oligosaccharide diphosphates. After release of the phospholipid residue by mild acid hydrolysis, the corresponding [14C]oligosaccharides were analyzed by gel-filtration, liquid chromatography, degradation by endo-N-acetyl-beta-D-glucosaminidases D and H, by jack bean alpha-D-mannosidase and Aspergillus oryzae (1----2)-alpha-D-mannosidase, acetolysis, and binding to concanavalin A-Sepharose. From the results it could be inferred that the following reaction took place in calf pancreas microsomes: alpha-D-Manp-(1----6)-beta-D-Manp-(1----4)-beta-D-GlcpNAc-(1 ----4)-alpha-D- GlcpNAc-PP-Dol + GDP-D-Man gave GDP + alpha-D-Manp-(1----3)-[alpha-D-Manp-(1----6)]-beta-D-Manp -(1----4)- beta-D-GlcpNAc-(1----4)-alpha-D-GlcpNAc-PP-Dol. The next products to be formed were alpha-D-Manp-(1----2)-alpha-D-Manp-(1----3)-[alpha-D-Manp -(1----6)]-beta-D- Manp-(1----4)-beta-D-GlcpNAc-(1----4)-alpha-D-GlcpNAc-PP-Dol, followed by alpha-D-Manp-(1----2)-alpha-D-Manp-(1----2)-alpha-D-Manp+ ++-(1----3)- [alpha-D-Manp-(1----6)]-beta-D-Manp-(1----4)-beta-D-GlcpNAc- (1----4)-alpha- D-GlcpNAc-PP-Dol. The mannose incorporation was enhanced by Triton X-100 and inhibited by Mn2+, and it occurred in the presence of either Mg2+ or EDTA. It is likely that the mannose donor was GDP-mannose since, under the conditions used, the formation of dolichyl mannosyl phosphate was negligible and the dolichyl heptasaccharide diphosphate accumulated.
用合成的α-D-甘露糖基-(1→6)-β-D-甘露糖基-(1→4)-β-D-葡萄糖胺基-N-乙酰-(1→4)-α-D-葡萄糖胺基-N-乙酰焦磷酸多萜醇和GDP-D-[14C]-甘露糖培育小牛胰腺微粒体,得到了三种主要的脂质连接寡糖二磷酸酯。通过温和酸水解释放磷脂残基后,通过凝胶过滤、液相色谱、内切-N-乙酰-β-D-葡萄糖胺糖苷酶D和H、刀豆α-D-甘露糖苷酶和米曲霉(1→2)-α-D-甘露糖苷酶降解、乙酰解以及与伴刀豆球蛋白A-琼脂糖结合等方法对相应的[14C]寡糖进行分析。从结果可以推断,在小牛胰腺微粒体中发生了以下反应:α-D-甘露糖基-(1→6)-β-D-甘露糖基-(1→4)-β-D-葡萄糖胺基-N-乙酰-(1→4)-α-D-葡萄糖胺基-N-乙酰焦磷酸多萜醇 + GDP-D-甘露糖 → GDP + α-D-甘露糖基-(1→3)-[α-D-甘露糖基-(1→6)]-β-D-甘露糖基-(1→4)-β-D-葡萄糖胺基-N-乙酰-(1→4)-α-D-葡萄糖胺基-N-乙酰焦磷酸多萜醇。接下来形成的产物是α-D-甘露糖基-(1→2)-α-D-甘露糖基-(1→3)-[α-D-甘露糖基-(1→6)]-β-D-甘露糖基-(1→4)-β-D-葡萄糖胺基-N-乙酰-(1→4)-α-D-葡萄糖胺基-N-乙酰焦磷酸多萜醇,随后是α-D-甘露糖基-(1→2)-α-D-甘露糖基-(1→2)-α-D-甘露糖基-(1→3)-[α-D-甘露糖基-(1→6)]-β-D-甘露糖基-(1→4)-β-D-葡萄糖胺基-N-乙酰-(1→4)-α-D-葡萄糖胺基-N-乙酰焦磷酸多萜醇。甘露糖的掺入被Triton X-100增强,被Mn2+抑制,并且在Mg2+或EDTA存在的情况下发生。甘露糖供体很可能是GDP-甘露糖,因为在所使用的条件下,多萜醇磷酸甘露糖的形成可以忽略不计,并且多萜醇七糖二磷酸积累。