Enantioselective enzymatic resolution of racemic alcohols by lipases in green organic solvents
Autor: | Stefano Serra, Francesco Secundo, Abderahmane Belafriekh, Zeineddine Djeghaba |
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Rok vydání: | 2017 |
Předmět: |
biology
010405 organic chemistry Organic Chemistry Cyclopentyl methyl ether green organic solvents Ether Primary alcohol 010402 general chemistry 01 natural sciences Catalysis 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound lipases chemistry Biocatalysis Ionic liquid Vinyl acetate biology.protein Organic chemistry Physical and Theoretical Chemistry Lipase Imide |
Zdroj: | Tetrahedron: asymmetry 28 (2017): 473–478. doi:10.1016/j.tetasy.2017.02.004 info:cnr-pdr/source/autori:Belafriekh A.; Secundo F.; Serra S.; Djeghaba Z./titolo:Enantioselective enzymatic resolution of racemic alcohols by lipases in green organic solvents/doi:10.1016%2Fj.tetasy.2017.02.004/rivista:Tetrahedron: asymmetry (Print)/anno:2017/pagina_da:473/pagina_a:478/intervallo_pagine:473–478/volume:28 |
ISSN: | 0957-4166 |
DOI: | 10.1016/j.tetasy.2017.02.004 |
Popis: | The effects of two eco-friendly solvents, 2-methyltetrahydrofuran (MeTHF) and cyclopentyl methyl ether (CPME), on the enzyme activity and enantioselectivity of Novozym 435, Candida rugosa lipase (CRL), Porcine pancreas lipase (PPL), Lipase AK, Lipase PS, and Lipozyme, a series of commercial lipases, in the enantioselective transesterfications of racemic menthol, racemic sulcatol and racemic α-cyclogeraniol were studied. Vinyl acetate was chosen as the acyl donor and the reactions were carried out at water activity 0.06. The activity of lipases in CPME was similar to that observed in other largely employed organic solvents [toluene and tert-butyl methyl ether (MTBE)], and was slightly lower in MeTHF. However, for most of the lipases tested, the enantioselectivity was higher in the eco-friendly solvents. Lipase AK exhibited a high enantioselectivity (E = 232) for the resolution of racemic menthol but the reaction rate was low. Lipase formulation (the enzyme was frozen and lyophilized in potassium phosphate buffer without and with 5% (w/v) of sucrose, d -mannitol, or methoxy poly(ethylene glycol)) was tested with this lipase in order to improve its activity, which increased up to 4.5 times, compared to the untreated enzyme. CALB was found to be a useful biocatalyst for the resolution of racemic sulcatol, where high activity and enantioselectivity were obtained (E ≥ 1000). For the resolution of the racemic primary alcohol α-cyclogeraniol, most of the lipases tested were active but not enantioselective, except lipase PS which displayed a moderate enantioselectivity (E = 19). The effect of the presence of a low percentage of two ionic liquids (ILs) 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIM][TFSI]) (5% (v/v)) and 1-Butyl-3-methylimidazoliumtetrafluoroborate ([BMIM][BF4]) (1% (v/v)) in the medium was also investigated. Only in the case of CRL the ILs slightly increased the enantioselectivity from E = 91 to E = 103 and E = 120 for [BMIM][TFSI] and [BMIM][BF4], respectively. However, in all cases ILs caused a decrease of enzyme activity. |
Databáze: | OpenAIRE |
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