State Key Laboratory of Food Science & Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, Jiangsu 214122, PR China.
State Key Laboratory of Food Science & Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, Jiangsu 214122, PR China.
Food Chem. 2017 May 1;222:105-112. doi: 10.1016/j.foodchem.2016.12.015. Epub 2016 Dec 10.
Glucansucrase was obtained from Lactobacillus reuteri SK24.003 and its characterizations and in vitro biosynthesis for glucose polymer and oligosaccharides were investigated. The final specific activity of glucansucrase was 1.3IU/mg protein with 8.6-fold purification and 8.7% recovery. The molecular weight of purified enzyme was 166.0kDa. The glucansucrase exhibited optimum activity at 30-35°C, whereas the maximum activity was obtained at pH 5.0-5.5. The double-charged ions including Mg, Mn, Ni, Co, Ca, Fe and Zn activated the glucansucrase activities and Ca ion highly stimulated the activity by approximately 4 times. K, V and k of purified glucansucrase were calculated to be 3.7mM, 0.8IU/mg and 18.21/s, respectively. For in vitro biosynthesis, glucansucrase synthesized 1,6-,1,4-α-d-glucan with a molecular weight of 2.5×10g/mol from sucrose as initial primer. Moreover, maltose acceptor-products synthesized by glucansucrase were composed of panose, maltotriose, maltotetraose, tetrasaccharide and pentasaccharide products analogues with an α-1,4/α-1,6 alternating structure.
从植物乳杆菌 SK24.003 中获得了葡聚糖蔗糖酶,并对其进行了性质鉴定及其在体外合成葡萄糖聚合物和低聚糖的研究。葡聚糖蔗糖酶的最终比活力为 1.3IU/mg 蛋白,经过 8.6 倍的纯化和 8.7%的回收率。纯化酶的分子量为 166.0kDa。葡聚糖蔗糖酶在 30-35°C 下表现出最佳活性,而在 pH5.0-5.5 时获得最大活性。包括 Mg、Mn、Ni、Co、Ca、Fe 和 Zn 在内的双电荷离子激活了葡聚糖蔗糖酶的活性,而 Ca 离子对活性的刺激作用约为 4 倍。纯化的葡聚糖蔗糖酶的 K、V 和 k 值分别计算为 3.7mM、0.8IU/mg 和 18.21/s。在体外生物合成中,葡聚糖蔗糖酶以蔗糖为初始引物合成了分子量为 2.5×10g/mol 的 1,6-、1,4-α-d-葡聚糖。此外,葡聚糖蔗糖酶合成的麦芽糖接受产物由潘糖、麦芽三糖、麦芽四糖、四糖和五糖产物组成,具有α-1,4/α-1,6 交替结构。