Determination, expression and characterization of an UDP-N-acetylglucosamine:α-1,3-D-mannoside β-1,2-N-acetylglucosaminyltransferase I (GnT-I) from the Pacific oyster, Crassostrea gigas.

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Julia Thoma, Reingard Grabherr, Erika Staudacher
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引用次数: 0

Abstract

Molluscs are intermediate hosts for several parasites. The recognition processes, required to evade the host's immune response, depend on carbohydrates. Therefore, the investigation of mollusc glycosylation capacities is of high relevance to understand the interaction of parasites with their host. UDP-N-acetylglucosamine:α-1,3-D-mannoside β-1,2-N-acetylglucosaminyltransferase I (GnT-I) is the key enzyme for the biosynthesis of hybrid and complex type N-glycans catalysing the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to the α-1,3 Man antenna of Man5GlcNAc2. Thereby, the enzyme produces a suitable substrate for further enzymes, such as α-mannosidase II, GlcNAc-transferase II, galactosyltransferases or fucosyltransferases. The sequence of GnT- I from the Pacific oyster, Crassostrea gigas, was obtained by homology search using the corresponding human enzyme as the template. The obtained gene codes for a 445 amino acids long type II transmembrane glycoprotein and shared typical structural elements with enzymes from other species. The enzyme was expressed in insect cells and purified by immunoprecipitation using protein A/G-plus agarose beads linked to monoclonal His-tag antibodies. GnT-I activity was determined towards the substrates Man5-PA, MM-PA and GnM-PA. The enzyme displayed highest activity at pH 7.0 and 30 °C, using Man5-PA as the substrate. Divalent cations were indispensable for the enzyme, with highest activity at 40 mM Mn2+, while the addition of EDTA or Cu2+ abolished the activity completely. The activity was also reduced by the addition of UDP, UTP or galactose. In this study we present the identification, expression and biochemical characterization of the first molluscan UDP-N-acetylglucosamine:α-1,3-D-mannoside β-1,2-N-acetylglucosaminyltransferase I, GnT-I, from the Pacific oyster Crassostrea gigas.

太平洋牡蛎(Crassostrea gigas)中一种 UDP-N-乙酰葡糖胺:α-1,3-D-甘露糖苷 β-1,2-N-乙酰葡糖胺基转移酶 I(GnT-I)的测定、表达和表征。
软体动物是多种寄生虫的中间宿主。躲避宿主免疫反应所需的识别过程依赖于碳水化合物。因此,研究软体动物的糖基化能力对于了解寄生虫与其宿主的相互作用具有重要意义。UDP-N-acetylglucosamine:α-1,3-D-mannoside β-1,2-N-acetylglucosaminyltransferase I(GnT-I)是混合型和复合型 N-聚糖生物合成的关键酶,它催化 N-乙酰葡糖胺从 UDP-N-acetylglucosamine 转移到 Man5GlcNAc2 的 α-1,3 Man 天线上。因此,该酶为其他酶,如α-甘露糖苷酶 II、GlcNAc-转移酶 II、半乳糖基转移酶或岩藻糖基转移酶提供了合适的底物。以相应的人类酶为模板,通过同源性搜索获得了太平洋牡蛎(Crassostrea gigas)的 GnT- I 基因序列。所获得的基因编码一种长 445 氨基酸的 II 型跨膜糖蛋白,与其他物种的酶具有相同的典型结构元素。该酶在昆虫细胞中表达,并通过与单克隆 His-tag 抗体相连的蛋白 A/G-plus 琼脂糖珠进行免疫沉淀纯化。测定了 GnT-I 对底物 Man5-PA、MM-PA 和 GnM-PA 的活性。以 Man5-PA 为底物,该酶在 pH 值为 7.0、温度为 30 ℃ 时活性最高。该酶离不开二价阳离子,在 40 mM Mn2+ 时活性最高,而加入 EDTA 或 Cu2+ 则完全丧失活性。加入 UDP、UTP 或半乳糖也会降低其活性。本研究首次从太平洋牡蛎(Crassostrea gigas)中鉴定、表达了软体动物 UDP-N-乙酰葡糖胺:α-1,3-D-甘露糖苷 β-1,2-N-乙酰葡糖胺基转移酶 I GnT-I,并对其进行了生化鉴定。
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来源期刊
Glycoconjugate Journal
Glycoconjugate Journal 生物-生化与分子生物学
CiteScore
6.00
自引率
3.30%
发文量
63
审稿时长
1 months
期刊介绍: Glycoconjugate Journal publishes articles and reviews on all areas concerned with: function, composition, structure, biosynthesis, degradation, interactions, recognition and chemo-enzymatic synthesis of glycoconjugates (glycoproteins, glycolipids, oligosaccharides, polysaccharides and proteoglycans), biochemistry, molecular biology, biotechnology, immunology and cell biology of glycoconjugates, aspects related to disease processes (immunological, inflammatory, arthritic infections, metabolic disorders, malignancy, neurological disorders), structural and functional glycomics, glycoimmunology, glycovaccines, organic synthesis of glycoconjugates and the development of methodologies if biologically relevant, glycosylation changes in disease if focused on either the discovery of a novel disease marker or the improved understanding of some basic pathological mechanism, articles on the effects of toxicological agents (alcohol, tobacco, narcotics, environmental agents) on glycosylation, and the use of glycotherapeutics. Glycoconjugate Journal is the official journal of the International Glycoconjugate Organization, which is responsible for organizing the biennial International Symposia on Glycoconjugates.
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