Chemický ústav, Slovenská akadémia vied, Dúbravská cesta 9, 845 38, Bratislava, Slovakia.
Glycoconj J. 2013 Dec;30(9):899-909. doi: 10.1007/s10719-013-9495-5. Epub 2013 Aug 25.
Homology searches indicated that up to five class I α-mannosidases (glycohydrolase family 47) and eight class II α-mannosidases (glycohydrolase family 38) are encoded by the fruitfly (Drosophila melanogaster) genome. Selected example mannosidases were expressed in secreted form using the yeast Pichia pastoris. A number of characteristics of these enzymes were determined with p-nitrophenyl-α-mannoside as substrate; particularly striking were the low optima (pH 5) of three class II mannosidases most closely related to known lysosomal mannosidases and the distinct Co(II)-requirement of a mannosidase previously named ManIIb. Some of the recombinant mannosidases were demonstrably active towards oligomannosidic glycans, specifically, the Co(II)-requiring ManIIb, two 'acidic' mannosidases and the class I mas-1 mannosidase. Other than previous characterisations of the well-known Golgi mannosidase II, this is the first study summarising various properties of recombinant mannosidases from the fruitfly.
同源性搜索表明,果蝇(Drosophila melanogaster)基因组编码了多达 5 种 I 类α-甘露糖苷酶(糖水解酶家族 47)和 8 种 II 类α-甘露糖苷酶(糖水解酶家族 38)。选择的甘露糖苷酶以分泌形式使用酵母毕赤酵母(Pichia pastoris)表达。使用 p-硝基苯基-α-甘露糖苷作为底物,确定了这些酶的许多特性;特别引人注目的是与已知溶酶体甘露糖苷酶最密切相关的三种 II 类甘露糖苷酶的低最适 pH 值(5),以及先前命名为 ManIIb 的甘露糖苷酶的独特 Co(II)需求。一些重组甘露糖苷酶对寡甘露糖基聚糖具有明显的活性,特别是 Co(II)需要的 ManIIb、两种“酸性”甘露糖苷酶和 I 类 mas-1 甘露糖苷酶。除了对著名的高尔基甘露糖苷酶 II 的先前表征外,这是首次总结来自果蝇的重组甘露糖苷酶的各种特性的研究。