Strasser R, Steinkellner H, Borén M, Altmann F, Mach L, Glössl J, Mucha J
Zentrum für Angewandte Genetik, Universität für Bodenkultur Wien, Austria.
Glycoconj J. 1999 Dec;16(12):787-91. doi: 10.1023/a:1007127815012.
N-acetylglucosaminyltransferase II (GnTII, EC 2.4.1.143) is a Golgi enzyme involved in the biosynthesis of glycoprotein-bound N-linked oligosaccharides, catalysing an essential step in the conversion of oligomannose-type to complex N-glycans. GnTII activity has been detected in both animals and plants. However, while cDNAs encoding the enzyme have already been cloned from several mammalian sources no GnTII homologue has been cloned from plants so far. Here we report the molecular cloning of an Arabidopsis thaliana GnTII cDNA with striking homology to its animal counterparts. The predicted domain structure of A. thaliana GnTII indicates a type II transmembrane protein topology as it has been established for the mammalian variants of the enzyme. Upon expression of A. thaliana GnTII cDNA in the baculovirus/insect cell system, a recombinant protein was produced that exhibited GnTII activity.
N-乙酰葡糖胺基转移酶II(GnTII,EC 2.4.1.143)是一种参与糖蛋白结合的N-连接寡糖生物合成的高尔基体酶,催化寡甘露糖型向复杂N-聚糖转化的关键步骤。在动物和植物中均检测到了GnTII活性。然而,虽然已经从多种哺乳动物来源克隆了编码该酶的cDNA,但迄今为止尚未从植物中克隆到GnTII同源物。在此,我们报道了拟南芥GnTII cDNA的分子克隆,其与动物对应物具有显著的同源性。拟南芥GnTII的预测结构域结构表明它是一种II型跨膜蛋白拓扑结构,就像该酶的哺乳动物变体一样。在杆状病毒/昆虫细胞系统中表达拟南芥GnTII cDNA后,产生了一种具有GnTII活性的重组蛋白。