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Thermostability Improvement of the d-Allulose 3-Epimerase from Dorea sp. CAG317 by Site-Directed Mutagenesis at the Interface Regions.
- Source :
-
Journal of agricultural and food chemistry [J Agric Food Chem] 2018 Jun 06; Vol. 66 (22), pp. 5593-5601. Date of Electronic Publication: 2018 May 29. - Publication Year :
- 2018
-
Abstract
- d-Allulose is a low-calorie sweetener and has broad applications in the food, cosmetics, and pharmaceutical industries. Recently, most studies focus on d-allulose production from d-fructose by d-allulose 3-epimerase (DAEase). However, the major blocker of industrial production of d-allulose is the poor thermostability. In this study, site-directed mutagenesis at the interface regions of Dorea sp. DAEase was carried out, and the F154Y/E191D/I193F mutation was obtained. The mutant protein displayed much higher thermostability, with a t <subscript>1/2</subscript> value of 20.47 h (50 °C) and a T <subscript>m</subscript> value of 74.18 °C. Compared with the wild-type DAEase, the t <subscript>1/2</subscript> value at 50 °C increased by 5.4-fold, and the T <subscript>m</subscript> value increased by 17.54 °C. In the d-allulose production from 500 g/L d-fructose, 148.2 g/L d-allulose could be obtained by F154Y/E191D/I193F mutant protein. The results suggest that site-directed mutagenesis at the interface regions is an efficient approach for improving the thermostability of DAEase.
- Subjects :
- Bacterial Proteins metabolism
Enzyme Stability
Firmicutes chemistry
Firmicutes genetics
Hot Temperature
Hydrogen-Ion Concentration
Kinetics
Mutagenesis, Site-Directed
Racemases and Epimerases metabolism
Bacterial Proteins chemistry
Bacterial Proteins genetics
Firmicutes enzymology
Fructose metabolism
Racemases and Epimerases chemistry
Racemases and Epimerases genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1520-5118
- Volume :
- 66
- Issue :
- 22
- Database :
- MEDLINE
- Journal :
- Journal of agricultural and food chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29762031
- Full Text :
- https://doi.org/10.1021/acs.jafc.8b01200