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首页> 外文期刊>Glycobiology. >Novel Schizosaccharomyces pombe N-linked GalMan9GlcNAc isomers: role of the Golgi GMA12 galactosyltransferase in core glycan galactosylation.
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Novel Schizosaccharomyces pombe N-linked GalMan9GlcNAc isomers: role of the Golgi GMA12 galactosyltransferase in core glycan galactosylation.

机译:新型粟酒裂殖酵母N-联的GalMan9GlcNAc异构体:高尔基GMA12半乳糖基转移酶在核心聚糖半乳糖基化中的作用。

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摘要

Schizosaccharomyces pombe synthesizes very large N-linked galactomannans, which are elongated from the Man9GlcNAc2 core that remains after the trimming of three Glc residues from the Glc3Man9GlcNAc2 originally transferred from dolichyl pyrophosphate to nascent proteins in the endoplasmic reticulum. Prior to elongation of the galactomannan outer chain, the Man9GlcNAc2 core is modified into a family of Hex10-15GlcNAc2 structures by the addition of both Gal and Man residues (Ziegler et al. (1994) J. Biol. Chem., 269, 12527-12535). To understand the pathway of Man9GlcNAc2 modification, the Hex10GlcNAc-sized pool was isolated by Bio-Gel P-4 gel filtration from the endo H-released N-glycans of S.pombe glycoproteins. This pool yielded four major fractions, a, b, c, and g, on preparative high pH, anion exchange chromatography, that represented 10, 29, 46, and 13% of the total Hex10GlcNAc present, respectively. Structures of the glycan isomers present in each fraction were determined by one- and two-dimensional 1H NMR spectroscopy techniques. Fraction a is principally (approximately 93%) a Man10GlcNAc with a new alpha1,2-linked Man cap on the upper-arm of Man9GlcNAc. Fraction b contained two isomers of GalMan9GlcNAc in which an alpha1,2-linked terminal Gal had been added either to the upper (b1, 30%) or middle-arm (b2, 70%) of Man9GlcNAc. The gma12 - alpha1,2-galactosyltransferase-negative S. pombe strain (Chappell et al. (1994) Mol. Biol. Cell., 5, 519-528) did not make fraction b implying that the gma12p galactosyltransferase is responsible for synthesis of both isomers b1 and b2. Isomer c is Man10GlcNAc in which a new branching alpha1, 6-linked Man had been added to the lower-arm alpha1,3-linked core residue as found earlier in Saccharomyces cerevisiae and Pichia pastoris. Fraction g had less than molar stoichiometry of both Gal and Glc. The major isomer (g1, 85%) is the Man9GlcNAc core with an alpha1,3-linked branching Gal on the penultimate 2-O-substituted Man of the lower arm. This residue is also found on a novel O-linked oligosaccharide recently described in S.pombe; Manalpha1,2(Galalpha1, 3)Manalpha1,2Mannitol (Gemmill and Trimble (1999) Glycobiology, 9, 507-515). The second isomer (g2, 15%) is the partially processed Glc2Man9GlcNAc intermediate. Defining these Hex10GlcNAc structures provides a starting point for understanding the enzymology of N-linked galactomannan core heterogeneity seen on S.pombe glycoproteins.
机译:裂殖酵母(Schizosaccharomyces pombe)合成了非常大的N-连接半乳甘露聚糖,其从Man9GlcNAc2核中延伸出来,而Man9GlcNAc2核被修剪后,最初将Glc3Man9GlcNAc2中的三个Glc残基从焦磷酸焦磷酸转移到内质网中的新生蛋白质上。在延长半乳甘露聚糖外链之前,通过同时添加Gal和Man残基将Man9GlcNAc2核心修饰为Hex10-15GlcNAc2结构家族(Ziegler等(1994)J。Biol。Chem。,269,12527- 12535)。为了了解Man9GlcNAc2修饰的途径,通过Bio-Gel P-4凝胶过滤从S.pombe糖蛋白的内H释放N-聚糖中分离了Hex10GlcNAc大小的库。在制备型高pH值阴离子交换色谱上,该库产生了四个主要馏分a,b,c和g,分别代表存在的Hex10GlcNAc总量的10%,29%,46%和13%。通过一维和二维1H NMR光谱技术确定每个馏分中存在的聚糖异构体的结构。分数a主要是(大约93%)Man10GlcNAc,在Man9GlcNAc的上臂上带有一个新的与alpha1,2连接的Man帽。馏分b包含GalMan9GlcNAc的两个异构体,其中已将α1,2连接的末端Gal添加到Man9GlcNAc的上臂(b1,30%)或中臂(b2,70%)中。 gma12-α1,2-半乳糖基转移酶阴性的粟酒裂殖酵母菌株(Chappell等(1994)Mol。Biol。Cell。,5,519-528)未产生级分b,这暗示gma12p半乳糖基转移酶负责合成两个异构体b1和b2。异构体c是Man10GlcNAc,其中已在较早的酿酒酵母和巴斯德毕赤酵母中发现了一个新的分支支链alpha1,6-连接的Man,已添加到下臂alpha1,3-连接的核心残基上。分数g小于Gal和Glc的摩尔化学计量。主要的异构体(g1,85%)是Man9GlcNAc核心,在下臂的倒数第二个2-O取代的Man上具有与α1,3-连接的分支Gal。最近在S.pombe中描述的新型O-连接的寡糖上也发现了该残基。 Manalpha1,2(Galalpha1,3)Manalpha1,2Mannitol(Gemmill and Trimble(1999)Glycobiology,9,507-515)。第二种异构体(g2,15%)是部分加工的Glc2Man9GlcNAc中间体。定义这些Hex10GlcNAc结构为理解S.pombe糖蛋白上N-连接的半乳​​甘露聚糖核心异质性的酶学提供了一个起点。

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