Fabrication of Ni2+-nitrilotriacetic acid functionalized magnetic mesoporous silica nanoflowers for one pot purification and immobilization of His-tagged ω-transaminase

被引:40
作者
Cao, Guangxiu [1 ,2 ]
Gao, Jing [1 ,2 ]
Zhou, Liya [1 ,2 ]
Huang, Zhihong [1 ,2 ]
He, Ying [1 ,2 ]
Zhu, Meng [1 ,2 ]
Jiang, Yanjun [1 ,2 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Tianjin 300130, Peoples R China
[2] Hebei Univ Technol, Hebei Prov Key Lab Green Chem Technol & High Effi, Tianjin 300130, Peoples R China
关键词
omega-transaminase; Immobilization; Magnetic mesoporous silica nanoflowers; Purification; ONE-STEP PURIFICATION; EFFICIENT PURIFICATION; PROTEIN-PURIFICATION; KINETIC RESOLUTION; FACILE SYNTHESIS; CHIRAL AMINES; NANOPARTICLES; AMINOTRANSFERASE; FE3O4-AT-SIO2; MICROSPHERES;
D O I
10.1016/j.bej.2017.09.019
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
omega-transaminase (omega-TA) has gained much attention due to its application in the preparation of chiral amines. It is of increasing interest to obtain stable and reusable immobilized omega-TA for economic catalytic process. A major approach for simple and efficient immobilization is introduction of an affinity tag to the target enzyme. Thus, in this study, the recombinant omega-TA with His-tag was successfully expressed in E.coli Rosetta (DE3). To realize the one pot purification and immobilization of omega-TA, Ni2+-nitrilotriacetic acid functionalized magnetic mesoporous silica nanoflowers (Ni-NTAIMMS-NF) were synthesized for the first time. The morphology, structure, and composition of the Ni-NTA/MMS-NF were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, etc. The immobilized omega-TA had the same optimum temperature with free omega-TA, and the optimum pH of the immobilized omega-TA was shifted from 7.5 to 7.0. Compared to free omega-TA, the immobilized omega-TA showed increased thermal stability, better pH stability, and excellent storage stability. Additionally, the immobilized omega-TA preserved 67.38% of initial activity after reusing twelve times. These results revealed that Ni-NTA/MMS-NF might have great potential in the purification and immobilization of His-tagged enzyme. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:116 / 125
页数:10
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