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粟酒裂殖酵母产生新型Gal0-2Man1-3 O-连接寡糖。

Schizosaccharomyces pombe produces novel Gal0-2Man1-3 O-linked oligosaccharides.

作者信息

Gemmill T R, Trimble R B

机构信息

Wadsworth Center, New York State Department of Health, Albany, NY 12201-0509, USA.

出版信息

Glycobiology. 1999 May;9(5):507-15. doi: 10.1093/glycob/9.5.507.

Abstract

Schizosaccharomyces pombe whole-cell glycoproteins, previously depleted of N-linked glycans by sequential treatment with endo-ss-N-acetylglucosaminidase H and peptide-N4-asparagine amidohydrolase F, were ss-eliminated with 0.1 M NaOH/1 M NaBH4 to release the O-linked oligosaccharides. The saccharide-alditols were separated by gel-exclusion chromatography into pools from Hexitol to Hex4Hexitol in size. Analysis of the Hexitol pool indicated Man to be the only sugar linked to Ser or Thr residues. The Hex1Hexitol pool contained two components, Galalpha1,2Man-ol (2A) and Manalpha1, 2Man-ol (2B). The Hex2Hexitol pool contained two components, Galalpha1,2Manalpha1,2Man-ol (3A) and Manalpha1,2Manalpha1,2Man-ol (3B). The two Hex3Hexitol components were Galalpha1,2(Galalpha1, 3)Manalpha1,2Man-ol (4A) and Manalpha1,2(Galalpha1,3)Manalpha1, 2Man-ol (4B). The Hex4Hexitol component was found to be a single isomer with the composition of Galalpha1,2(Galalpha1,3)Manalpha1, 2Manalpha1,2Man-ol (5AB). Surprisingly, galactobiose was not detected in any of these oligosaccharides. The gma12 (T. G. Chappell and G. Warren (1989) J. Cell Biol., 109, 2693-2707) and gth1 (T. G. Chappell personal communication) alpha1, 2-galactosyltransferase-deficient mutants and the gma12/gth1 double mutant S.pombe strains were similarly examined. The results indicated that gma12p is solely responsible for the addition of terminal alpha1,2-linked Gal in compound 2A, while one or both of gma12p and gth1p are required for the alpha1,2-linked Gal in 4A. Both transferases are largely responsible for terminal Gal in isomer 5AB. Neither gma12 nor gth1 had any discernible effect on the structure of the large N-linked galactomannans as determined by 1H NMR spectroscopy. Thus, while gth1p and gma12p appear responsible for adding alpha1,2-linked Gal to terminal Man, neither adds galactose side chains to the N-linked poly alpha1,6-Man outerchain, nor the O-linked branch-forming alpha1,3-linked Gal. Furthermore, the presence of Hexalpha1,2(Galalpha1,3)Manalpha1,2- structures in the O-linked glycans implies the presence of a novel branch-forming alpha1,3-galactosyltransferase in S.pombe.

摘要

粟酒裂殖酵母全细胞糖蛋白,先前已通过用内切-β-N-乙酰葡糖胺糖苷酶H和肽-N4-天冬酰胺酶F顺序处理去除了N-连接聚糖,用0.1 M NaOH/1 M NaBH4进行β-消除以释放O-连接寡糖。糖醛糖醇通过凝胶排阻色谱法按大小从己糖醇到己四醇分为不同组分。对己糖醇组分的分析表明,甘露糖是唯一与丝氨酸或苏氨酸残基相连的糖。己一醇组分包含两个成分,即Galα1,2Man-ol(2A)和Manα1,2Man-ol(2B)。己二醇组分包含两个成分,即Galα1,2Manα1,2Man-ol(3A)和Manα1,2Manα1,2Man-ol(3B)。两个己三醇成分是Galα1,2(Galα1,3)Manα1,2Man-ol(4A)和Manα1,2(Galα1,3)Manα1,2Man-ol(4B)。发现己四醇成分是一种单一异构体,其组成为Galα1,2(Galα1,3)Manα1,2Manα1,2Man-ol(5AB)。令人惊讶的是,在这些寡糖中均未检测到半乳糖二糖。对gma12(T.G.Chappell和G.Warren(1989年)《细胞生物学杂志》,109卷,2693 - 2707页)和gth1(T.G.Chappell个人通讯)α1,2-半乳糖基转移酶缺陷型突变体以及gma12/gth1双突变粟酒裂殖酵母菌株进行了类似的检测。结果表明,gma12p单独负责在化合物2A中添加末端α1,2-连接的半乳糖,而在4A中α1,2-连接的半乳糖需要gma12p和gth1p中的一个或两个。两种转移酶在很大程度上负责异构体5AB中的末端半乳糖。通过1H NMR光谱法测定,gma12和gth1对大的N-连接半乳甘露聚糖的结构均无明显影响。因此,虽然gth1p和gma12p似乎负责将α1,2-连接的半乳糖添加到末端甘露糖上,但两者均未向N-连接的多α1,6-甘露糖外链或O-连接的形成分支的α1,3-连接的半乳糖添加半乳糖侧链。此外,O-连接聚糖中Hexα1,2(Galα1,3)Manα1,2-结构的存在意味着粟酒裂殖酵母中存在一种新型的形成分支的α1,3-半乳糖基转移酶。

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