首页> 外文期刊>The FEBS journal >Aspergillus nidulans alpha-galactosidase of glycoside hydrolase family 36 catalyses the formation of alpha-galacto-oligosaccharides by transglycosylation.
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Aspergillus nidulans alpha-galactosidase of glycoside hydrolase family 36 catalyses the formation of alpha-galacto-oligosaccharides by transglycosylation.

机译:糖苷水解酶家族36的构巢曲霉α-半乳糖苷酶通过转糖基化催化α-半乳糖寡糖的形成。

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摘要

The alpha-galactosidase from Aspergillus nidulans (AglC) belongs to a phylogenetic cluster containing eukaryotic alpha-galactosidases and alpha-galacto-oligosaccharide synthases of glycoside hydrolase family 36 (GH36). The recombinant AglC, produced in high yield (0.65 g.L-1 culture) as His-tag fusion in Escherichia coli, catalysed efficient transglycosylation with alpha-(1 rightwards-arrow 6) regioselectivity from 40 mM 4-nitrophenol alpha-D-galactopyranoside, melibiose or raffinose, resulting in a 37-74% yield of 4-nitrophenol alpha-D-Galp-(1 rightwards-arrow 6)-D-Galp, alpha-D-Galp-(1 rightwards-arrow 6)- alpha-D-Galp-(1 rightwards-arrow 6)-D-Glcp and alpha-D-Galp-(1 rightwards-arrow 6)- alpha-D-Galp-(1 rightwards-arrow 6)-D-Glcp-( alpha1 rightwards-arrow beta2)-D-Fruf (stachyose), respectively. Furthermore, among 10 monosaccharide acceptor candidates (400 mM) and the donor 4-nitrophenol alpha-D-galactopyranoside (40 mM), alpha-(1 rightwards-arrow 6) linked galactodisaccharides were also obtained with galactose, glucose and mannose in high yields of 39-58%. AglC did not transglycosylate monosaccharides without the 6-hydroxymethyl group, i.e. xylose, L-arabinose, L-fucose and L-rhamnose, or with axial 3-OH, i.e. gulose, allose, altrose and L-rhamnose. Structural modelling using Thermotoga maritima GH36 alpha-galactosidase as the template and superimposition of melibiose from the complex with human GH27 alpha-galactosidase supported that recognition at subsite +1 in AglC presumably requires a hydrogen bond between 3-OH and Trp358 and a hydrophobic environment around the C-6 hydroxymethyl group. In addition, successful transglycosylation of eight of 10 disaccharides (400 mM), except xylobiose and arabinobiose, indicated broad specificity for interaction with the +2 subsite. AglC thus transferred alpha-galactosyl to 6-OH of the terminal residue in the alpha-linked melibiose, maltose, trehalose, sucrose and turanose in 6-46% yield and the beta-linked lactose, lactulose and cellobiose in 28-38% yield. The product structures were identified using NMR and ESI-MS and five of the 13 identified products were novel, i.e. alpha-D-Galp-(1 rightwards-arrow 6)-D-Manp; alpha-D-Galp-(1 rightwards-arrow 6)- beta-D-Glcp-(1 rightwards-arrow 4)-D-Glcp; alpha-D-Galp-(1 rightwards-arrow 6)- beta-D-Galp-(1 rightwards-arrow 4)-D-Fruf; alpha-D-Galp-(1 rightwards-arrow 6)-D-Glcp-( alpha1 rightwards-arrow alpha1)-D-Glcp; and alpha-D-Galp-(1 rightwards-arrow 6)- alpha-D-Glcp-(1 rightwards-arrow 3)-D-Fruf
机译:来自构巢曲霉(AglC)的α-半乳糖苷酶属于系统发育簇,其包含糖苷水解酶家族36(GH36)的真核α-半乳糖苷酶和α-半乳糖寡糖合酶。以大肠杆菌中的His-tag融合物的高产量(0.65 gL-1培养物)产生的重组AglC催化了来自40 mM 4-硝基苯酚α-D-吡喃半乳糖苷的α-(1向右箭头6)区域选择性的高效转糖基作用, melibiose或棉子糖,产生4-硝基苯酚α-D-Galp-(1向右箭头6)-D-Galp,α-D-Galp-(1向右箭头6)-alpha- D-Galp-(1向右箭头6)-D-Glcp和alpha-D-Galp-(1向右箭头6)-alpha-D-Galp-(1向右箭头6)-D-Glcp-(alpha1向右箭头beta2)-D-Fruf(水苏糖)。此外,在10个单糖受体候选物(400 mM)和供体4-硝基苯酚α-D-半乳糖吡喃糖苷(40 mM)中,还获得了半乳糖,葡萄糖和甘露糖高产量的α-(1向右箭头6)连接的半乳​​糖。 39-58%。没有6-羟甲基基团的木糖,即木糖,L-阿拉伯糖,L-岩藻糖和L-鼠李糖,或具有轴向的3-OH,即果糖,Allose,altrose和L-鼠李糖,AglC不会对糖基进行转糖基化。使用海栖嗜热菌GH36α-半乳糖苷酶作为模板进行结构建模,并将复合物中的半胱氨酸与人GH27α-半乳糖苷酶叠加,支持在AglC的+1位亚基处进行识别可能需要在3-OH和Trp358之间存在氢键以及周围的疏水环境C-6羟甲基。此外,除木糖和阿拉伯糖以外的10种二糖中的8种(400 mM)成功进行了糖基转移,表明与+2亚位点的相互作用具有广泛的特异性。因此,AglC以6-46%的产率将α-半乳糖基转移至α-连接的角叉果糖,麦芽糖,海藻糖,蔗糖和松二糖的末端残基的6-OH,β-连接的乳糖,乳果糖和纤维二糖的产率为28-38%。 。用NMR和ESI-MS鉴定产物结构,鉴定出的13种产物中有5种是新颖的,即α-D-Galp-(1向右箭头6)-D-Manp。 alpha-D-Galp-(1向右箭头6)-beta-D-Glcp-(1向右箭头4)-D-Glcp; alpha-D-Galp-(1向右箭头6)-beta-D-Galp-(1向右箭头4)-D-Fruf; alpha-D-Galp-(1向右箭头6)-D-Glcp-(alpha1向右箭头alpha1)-D-Glcp;和alpha-D-Galp-(1向右箭头6)-alpha-D-Glcp-(1向右箭头3)-D-Fruf

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