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Converting Galactose into the Rare Sugar Talose with Cellobiose 2-Epimerase as Biocatalyst.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2018 Oct 01; Vol. 23 (10). Date of Electronic Publication: 2018 Oct 01. - Publication Year :
- 2018
-
Abstract
- Cellobiose 2-epimerase from Rhodothermus marinus ( Rm CE) reversibly converts a glucose residue to a mannose residue at the reducing end of β-1,4-linked oligosaccharides. In this study, the monosaccharide specificity of Rm CE has been mapped and the synthesis of d-talose from d-galactose was discovered, a reaction not yet known to occur in nature. Moreover, the conversion is industrially relevant, as talose and its derivatives have been reported to possess important antimicrobial and anti-inflammatory properties. As the enzyme also catalyzes the keto-aldo isomerization of galactose to tagatose as a minor side reaction, the purity of talose was found to decrease over time. After process optimization, 23 g/L of talose could be obtained with a product purity of 86% and a yield of 8.5% (starting from 4 g (24 mmol) of galactose). However, higher purities and concentrations can be reached by decreasing and increasing the reaction time, respectively. In addition, two engineering attempts have also been performed. First, a mutant library of Rm CE was created to try and increase the activity on monosaccharide substrates. Next, two residues from Rm CE were introduced in the cellobiose 2-epimerase from Caldicellulosiruptor saccharolyticus ( Cs CE) (S99M/Q371F), increasing the k <subscript>cat</subscript> twofold.
- Subjects :
- Carbohydrate Epimerases genetics
Catalysis
Cellobiose chemistry
Computer Simulation
Gene Library
Hexoses chemistry
Isomerism
Kinetics
Monosaccharides chemistry
Mutation
Oligosaccharides chemistry
Substrate Specificity
Carbohydrate Epimerases chemistry
Galactose chemistry
Lactones chemistry
Rhodothermus enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 23
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 30275414
- Full Text :
- https://doi.org/10.3390/molecules23102519