Programming an Orthogonal Self-Assembling Protein Cascade Based on Reactive Peptide-Protein Pairs for In Vitro Enzymatic Trehalose Production

被引:29
作者
Chen, Xianhan [1 ]
Chen, Xinyi [1 ]
Zhu, Liying [2 ]
Liu, Wei [3 ]
Jiang, Ling [3 ]
机构
[1] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Jiangsu, Peoples R China
[2] Nanjing Tech Univ, Sch Chem & Mol Engn, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Coll Food Sci & Light Ind, Nanjing 211816, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
trehalose; protein scaffold; coimmobilization; modular self-assembly; biocatalysis; in vitro enzyme cascade; SYNTHASE; IMMOBILIZATION; COIMMOBILIZATION; THERMOSTABILITY; BIOCATALYSIS; MECHANISMS; SCAFFOLDS; INSIGHTS; ENZYMES; SYSTEM;
D O I
10.1021/acs.jafc.2c01118
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
: Trehalose is an important rare sugar that protects biomolecules against environmental stress. We herein introduce a dual enzyme cascade strategy that regulates the proportion of cargos and scaffolds, to maximize the benefits of enzyme immobilization. Based upon the self-assembling properties of the shell protein (EutM) from the ethanolamine utilization (Eut) bacterial microcompartment, we implemented the catalytic synthesis of trehalose from soluble starch with the coimmobilization of alpha amylase and trehalose synthase. This strategy improved enzymatic cascade activity and operational stability. The cascade system enabled the efficient production of trehalose with a yield of similar to 3.44 g/(L U), 1.5 times that of the free system. Moreover, its activity was maintained over 12 h, while the free system was almost completely inactivated after 4 h, demonstrating significantly enhanced thermostability. In conclusion, an attractive self-assembly coimmobilization platform was developed, which provides an effective biological process for the enzymatic synthesis of trehalose in vitro
引用
收藏
页码:4690 / 4700
页数:11
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