Aspergillus nidulansα-galactosidase of glycoside hydrolase family 36 catalyses the formation of α-galacto-oligosaccharides by transglycosylation

被引:41
作者
Nakai, Hiroyuki [1 ]
Baumann, Martin J. [1 ]
Petersen, Bent O. [2 ]
Westphal, Yvonne [3 ]
Abou Hachem, Maher [1 ]
Dilokpimol, Adiphol [1 ]
Duus, Jens O. [2 ]
Schols, Henk A. [3 ]
Svensson, Birte [1 ]
机构
[1] Tech Univ Denmark, Dept Syst Biol, DK-2800 Lyngby, Denmark
[2] Carlsberg Lab, Valby, Denmark
[3] Wageningen Univ, Food Chem Lab, Wageningen, Netherlands
关键词
acceptor specificity; carbohydrate structural analysis; transglycosylation; alpha-galacto-oligosaccharides; alpha-galactosidase; MOLECULAR-CLONING; BIFIDOBACTERIUM-ADOLESCENTIS; N-ACETYLGALACTOSAMINIDASE; ESCHERICHIA-COLI; PICHIA-PASTORIS; PHANEROCHAETE-CHRYSOSPORIUM; CLOSTRIDIUM-PERFRINGENS; FUNCTIONAL EXPRESSION; LACTOBACILLUS-REUTERI; THERMOTOGA-MARITIMA;
D O I
10.1111/j.1742-4658.2010.07763.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 center dot L-1 culture) as His-tag fusion in Escherichia coli, catalysed efficient transglycosylation with alpha-(1 -> 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 -> 6)-d-Galp, alpha-d-Galp-(1 -> 6)-alpha-d-Galp-(1 -> 6)-d-Glcp and alpha-d-Galp-(1 -> 6)-alpha-d-Galp-(1 -> 6)-d-Glcp-(alpha 1 ->beta 2)-d-Fruf (stachyose), respectively. Furthermore, among 10 monosaccharide acceptor candidates (400 mm) and the donor 4-nitrophenol alpha-d-galactopyranoside (40 mm), alpha-(1 -> 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 -> 6)-d-Manp; alpha-d-Galp-(1 -> 6)-beta-d-Glcp-(1 -> 4)-d-Glcp; alpha-d-Galp-(1 -> 6)-beta-d-Galp-(1 -> 4)-d-Fruf; alpha-d-Galp-(1 -> 6)-d-Glcp-(alpha 1 ->alpha 1)-d-Glcp; and alpha-d-Galp-(1 -> 6)-alpha-d-Glcp-(1 -> 3)-d-Fruf.
引用
收藏
页码:3538 / 3551
页数:14
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