Trinchera M, Pirovano B, Ghidoni R
Department of Medical Chemistry and Biochemistry, Medical School, University of Milan, Italy.
J Biol Chem. 1990 Oct 25;265(30):18242-7.
Using a sucrose density gradient fractionation of a highly purified Golgi apparatus from rat liver, we determined the sub-Golgi distribution of CMP-NeuAc:GM3 ganglioside alpha 2----8sialyltransferase (GM3-SAT) and CMP-NeuAc:GT1b ganglioside alpha 2----8sialyltransferase (GT1b-SAT), in comparison with that of the other glycosyltransferase activities involved in ganglioside biosynthesis. While GM3-SAT was recovered in several density fractions, GT1b-SAT was mainly found on less dense sub-Golgi membranes; this indicates that these two activities are physically separate. Moreover, with regard to the monosialo pathway, CMP-NeuAc:lactosylceramide alpha 2----3sialyltransferase, UDP-GalNAc:GM3 ganglioside beta 1----4N-acetylgalactosaminyltransferase, UDP-Gal:GM2 ganglioside beta 1----3galactosyltransferase, and CMP-NeuAc:GM1 ganglioside alpha 2----3sialyltransferase were resolved from more dense to less dense fractions, respectively. In the disialo pathway, UDP-GalNAc:GD3 ganglioside beta 1----4N-acetylgalactosaminyltransferase, UDP-Gal:GD2 ganglioside beta 1----3galactosyltransferase and CMP-NeuAc:GD1b ganglioside alpha 2----3sialyltransferase co-distributed with the corresponding activities of the monosialo pathway. These last results indicate that many Golgi glycosyltransferases involved in ganglioside biosynthesis are localized in the order in which they act.
利用大鼠肝脏高度纯化的高尔基体进行蔗糖密度梯度分级分离,我们确定了CMP-唾液酸:GM3神经节苷脂α2----8唾液酸转移酶(GM3-SAT)和CMP-唾液酸:GT1b神经节苷脂α2----8唾液酸转移酶(GT1b-SAT)的高尔基体亚分布,并与神经节苷脂生物合成中涉及的其他糖基转移酶活性进行了比较。虽然GM3-SAT在几个密度级分中被回收,但GT1b-SAT主要存在于密度较低的高尔基体亚膜上;这表明这两种活性在物理上是分开的。此外,关于单唾液酸途径,CMP-唾液酸:乳糖基神经酰胺α2----3唾液酸转移酶、UDP-GalNAc:GM3神经节苷脂β1----4N-乙酰半乳糖胺基转移酶、UDP-Gal:GM2神经节苷脂β1----3半乳糖基转移酶和CMP-唾液酸:GM1神经节苷脂α2----3唾液酸转移酶分别从密度较高的级分解析到密度较低的级分。在双唾液酸途径中,UDP-GalNAc:GD3神经节苷脂β1----4N-乙酰半乳糖胺基转移酶、UDP-Gal:GD2神经节苷脂β1----3半乳糖基转移酶和CMP-唾液酸:GD1b神经节苷脂α2----3唾液酸转移酶与单唾液酸途径的相应活性共分布。这些最后的结果表明,许多参与神经节苷脂生物合成的高尔基体糖基转移酶按其作用顺序定位。