Université de Toulouse; INSA, UPS, INP; LISBP, 135 Avenue de Rangueil, F-31077 Toulouse, France.
Carbohydr Polym. 2013 Apr 15;94(1):567-76. doi: 10.1016/j.carbpol.2013.01.064. Epub 2013 Jan 28.
GBD-CD2, an engineered sucrose-acting enzyme of glycoside hydrolase family 70, transfers D-glucopyranosyl (D-Glcp) units from sucrose onto dextrans or gluco-oligosaccharides (GOS) through the formation of α-(1→2) linkages leading to branched products of interest for health, food and cosmetic applications. Structural characterization of the branched products obtained from sucrose and pure GOS of degree of polymerization (DP) 4 or DP 5 revealed that highly α-(1→2) branched and new molecular structures can be synthesized by GBD-CD2. The formation of α-(1→2) branching is kinetically controlled and can occur onto vicinal α-(1→6)-linked D-Glcp residues. To investigate the mode of branching of 1.5 kDa dextran, simulations of various branching scenarios and resistance to glucoamylase degradation were performed. Analysis of the simulation results suggests that the branching process is stochastic and indicates that the enzyme acceptor site can accommodate both linear and poly-branched acceptors. This opens the way to the design of novel enzyme-based processes yielding carbohydrate structures varying in size and resistance to hydrolytic enzymes.
GBD-CD2 是一种经过工程改造的蔗糖作用酶,属于糖苷水解酶家族 70,通过形成 α-(1→2) 键,将 D-吡喃葡萄糖基(D-Glcp)单元从蔗糖转移到葡聚糖或葡萄糖低聚糖(GOS)上,从而得到具有健康、食品和化妆品应用价值的支化产物。对由蔗糖和聚合度(DP)为 4 或 DP 5 的纯 GOS 获得的支化产物进行结构表征,表明 GBD-CD2 可以合成高度 α-(1→2) 支化的新型分子结构。α-(1→2) 支化的形成是动力学控制的,并且可以发生在相邻的 α-(1→6)-连接的 D-Glcp 残基上。为了研究 1.5 kDa 葡聚糖的支化模式,对各种支化场景进行了模拟,并对其抵抗葡萄糖淀粉酶降解的能力进行了研究。模拟结果分析表明,支化过程是随机的,表明酶的受体部位可以容纳线性和多支化的受体。这为设计新型基于酶的工艺开辟了道路,这些工艺可以产生在大小和对水解酶的抗性方面有所不同的碳水化合物结构。