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Enzymatic regioselective acylation of nucleosides in biomass-derived 2-methyltetrahydrofuran: Kinetic study and enzyme substrate recognition

Paper ID Volume ID Publish Year Pages File Format Full-Text
23565 43452 2013 6 PDF Available
Title
Enzymatic regioselective acylation of nucleosides in biomass-derived 2-methyltetrahydrofuran: Kinetic study and enzyme substrate recognition
Abstract

Enzymatic regioselective acylation of pyrimidine nucleosides was mediated by immobilized lipase from Penicillium expansum in 2-methyltetrahydrofuran (MeTHF), a bio-solvent derived from biomass. Despite of the moderate dissolution ability of MeTHF toward nucleosides, the initial enzymatic reaction rate was much higher in this eco-friendly solvent than in other commonly used organic solvents. This could be explained by the lower apparent activation energy of the enzymatic reaction (24.5 vs. 43.3–57.1 kJ/mol) and the higher catalytic efficiency of the enzyme (Vmax/Km, 5.8 vs. 1.1–2.9 h−1) in MeTHF. The enzymatic acylation of a group of ribonucleosides afforded the desirable 5′-esters with the conversions of 96–99% and 5′-regioselectivities of 96 to >99%. In enzymatic acylation of 2′-deoxynucleosides, however, 5′-regioselectivities showed a clear dependence on the 5-substituents present in the base moiety although the substrate conversions reached >98% within 1–3 h. In the cases of 2′,3′-dideoxynucleoside analogs, the reaction rate decreased markedly due to the lack of 3′-hydroxyl.

► Much higher enzyme activity in MeTHF than in other organic solvents. ► Much lower apparent activation energy in this bio-solvent. ► Much higher catalytic efficiency (Vmax/Km) of the enzyme in MeTHF. ► First recognition study of Penicillium expansum lipase toward pyrimidine nucleosides.

Keywords
Bio-solvents; Enzymatic acylation; Nucleosides; Penicillium expansum lipase; Regioselectivity
First Page Preview
Enzymatic regioselective acylation of nucleosides in biomass-derived 2-methyltetrahydrofuran: Kinetic study and enzyme substrate recognition
Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Biotechnology - Volume 164, Issue 1, 10 March 2013, Pages 91–96
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering