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Increased Selectivity of Novozym 435 in the Asymmetric Hydrolysis of a Substrate with High Hydrophobicity Through the Use of Deep Eutectic Solvents and High Substrate Concentrations.
Fredes, Yerko; Chamorro, Lesly; Cabrera, Zaida.
Afiliação
  • Fredes Y; School of Biochemical Engineering, Pontificia Universidad Católica de Valparaíso; Avda. Brasil 2085 Valparaíso, Chile. y.a.fredes@gmail.com.
  • Chamorro L; School of Biochemical Engineering, Pontificia Universidad Católica de Valparaíso; Avda. Brasil 2085 Valparaíso, Chile. leslychamorromolina@gmail.com.
  • Cabrera Z; School of Biochemical Engineering, Pontificia Universidad Católica de Valparaíso; Avda. Brasil 2085 Valparaíso, Chile. zaida.cabrera@pucv.cl.
Molecules ; 24(4)2019 Feb 22.
Article em En | MEDLINE | ID: mdl-30813241
The effects of the reaction medium and substrate concentration were studied on the selectivity of Novozym 435 using the asymmetric hydrolysis of dimethyl-3-phenylglutarate as a model reaction. Results show that the use of choline chloride ChCl:urea/phosphate buffer 50% (v/v) as a reaction medium increased the selectivity of Novozym 435 by 16% (e.e = 88%) with respect to the one in 100% phosphate buffer (e.e = 76%). Best results were obtained when high substrate concentrations (well above the solubility limit, 27-fold) and ChCl:urea/phosphate buffer 50% (v/v) as reaction medium at pH 7 and 30 °C were used. Under such conditions, the R-monoester was produced with an enantiomeric purity of 99%. Novozym 435 was more stable in ChCl:urea/phosphate buffer 50% (v/v) than in phosphate buffer, retaining a 50% of its initial activity after 27 h of incubation at pH 7 and 40 °C. Results suggest that the use of deep eutectic solvents (ChCl:urea/phosphate buffer) in an heterogeneous reaction system (high substrate concentration) is a viable and promising strategy for the synthesis of chiral drugs from highly hydrophobic substrates.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Solventes / Colina / Glutaratos / Lipase Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Chile País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Solventes / Colina / Glutaratos / Lipase Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Chile País de publicação: Suíça