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High-level expression of Thermobifida fusca glucose isomerase for high fructose corn syrup biosynthesis.

Authors :
Zhu F
Deng H
He X
Song X
Chen N
Wang W
Source :
Enzyme and microbial technology [Enzyme Microb Technol] 2020 Apr; Vol. 135, pp. 109494. Date of Electronic Publication: 2019 Dec 13.
Publication Year :
2020

Abstract

Glucose isomerase (GIase), an efficient enzyme in the isomerization of d-glucose to d-fructose, has been widely used in food processing. In this study, an efficient expression system for a Thermobifida fusca GIase (GIase <subscript>Tfus</subscript> ) in Escherichia coli was firstly designed via a two-stage feeding strategy for improving expression level. The cultivation strategy was performed at an exponential feeding rate during the pre-induction phase, followed by a gradient-decreasing feeding rate at the induction phase in a 3-L fermenter. During this process, the effect of induction conditions and the complex nitrogen supplementation in feeding solutions on GIase <subscript>Tfus</subscript> production were investigated and optimized. Under the optimal conditions, the yield of GIase <subscript>Tfus</subscript> reached 124.1 U/mL, which is the highest expression level of GIase by recombinant E. coli reported to date. Additionally, the obtained GIase <subscript>Tfus</subscript> was performed to produce high fructose corn syrup (HFCS) with conversion approacing 55 % from glucose (45 %, w/v) to fructose. According to the molecular dynamic simulation, a number of hydrogen bonds existed in the enzyme-substrate complex could stablilize the transient states, and a appreciate reaction distance of M1 catalytic site and oxygen atom of glucose make the reaction proceed easily, thus resulting in the efficient biosynthesis of HFCS. The function of GIase <subscript>Tfus</subscript> renders it a valuable catalyst for HFCS-55 (containing 55 % d-fructose) manufacturing, the most favorable industrial product of HFCS. The efficient expression of GIase <subscript>Tfus</subscript> and its efficient HFCS production lays the foundation for its proming industrial application.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1879-0909
Volume :
135
Database :
MEDLINE
Journal :
Enzyme and microbial technology
Publication Type :
Academic Journal
Accession number :
32146933
Full Text :
https://doi.org/10.1016/j.enzmictec.2019.109494