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从粘膜炎莫拉氏菌中分离的支链淀粉酶的异源表达、分子修饰及其在塔格糖制备中的应用。

Heterogeneous expression, molecular modification of amylosucrase from Neisseria polysaccharea, and its application in the preparation of turanose.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, China; School of Biotechnology and Key Laboratory of Industrial Biotechnology Ministry of Education, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, China; International Joint Laboratory on Food Safety, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, China.

State Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, China; School of Biotechnology and Key Laboratory of Industrial Biotechnology Ministry of Education, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, China; International Joint Laboratory on Food Safety, Jiangnan University, 1800 Lihu Avenue, Wuxi 214122, China.

出版信息

Food Chem. 2020 Jun 1;314:126212. doi: 10.1016/j.foodchem.2020.126212. Epub 2020 Jan 13.

Abstract

Turanose, a potential novel sweetener in food industry, can be synthesized by Neisseria polysaccharea amylosucrase (NpAS). However, the malt-oligosaccharide byproduct affects the yield. In this study, the NpAS mutant G396S, which was expected to interfer with the extension of glucan by increasing steric hindrance, was obtained. The NpAS and G396S were heterologously expressed in Bacillus subtilis and enzyme properties were analyzed. Results showed that the polymerization activity of G396S was decreased. In addition, the mutant was used in the preparation of turanose. When using 2 M sucrose as substrate, the turanose yield reached 410.4 g·L, an increase of 61 g·L compared with that of NpAS. When fructose was added, the optimal fructose concentration for G396S decreased from 0.75 M to 0.5 M. The turanose production reached 523 g·L with the conversion rate of 76.5%. This study contributes the use of turanose in food industry.

摘要

塔洛糖是一种有潜力的新型食品甜味剂,可由唾液奈瑟菌淀粉酶(NpAS)合成。然而,麦芽低聚糖副产物会影响产量。本研究获得了 NpAS 突变体 G396S,预期通过增加空间位阻来干扰葡聚糖的延伸。NpAS 和 G396S 在枯草芽孢杆菌中异源表达,并分析了酶的性质。结果表明,G396S 的聚合活性降低。此外,该突变体用于塔洛糖的制备。当使用 2 M 蔗糖作为底物时,塔洛糖的产率达到 410.4 g·L,比 NpAS 提高了 61 g·L。添加果糖时,G396S 的最佳果糖浓度从 0.75 M 降低到 0.5 M。塔洛糖的产量达到 523 g·L,转化率为 76.5%。本研究为塔洛糖在食品工业中的应用提供了依据。

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