Puede utilizar el filtro de búsqueda del panel izquierdo para acotar los resultados
Filtro
Tipo de publicación
Todos Libros Revistas
Título
Autor
Palabras clave
ISBN
Acceso DOI
Acceso digital CSIC
Buscar
Datos técnicos
RevistaProcess Biochemistry
Año2011
Volumen46
Páginas2311–2316
Internacional

Rapid and high yield of synthesis of butyl acetate catalyzed by Novozym 435: reaction optimization by response surface methodology

Autores:Roberto Fernandez-Lafuente
Grupos de investigación:Optimización de biocatalizadores y bioprocesos enzimáticos
Martins, A.B. , Graebin, N.G. , Lorenzoni, A.S.G. , Fernandez-Lafuente, R. , Ayub, M.A.Z. , Rodrigues, R.C.


AFFILIATIONS: Biocatalysis and Enzyme Technology Lab, Institute of Food Science and Technology, Federal University of Rio Grande Do sul State, Av. Bento Gonalves, 9500 P.O. Box 15090, ZC 91501-970 Porto Alegre, RS, Brazil; 
Biochemical Engineering Lab (BiotecLab), Institute of Food Science and Technology, Federal University of Rio Grande Do sul State, Av. Bento Gonalves, 9500 P.O. Box 15090, ZC 91501-970 Porto Alegre, RS, Brazil; 
Department of Biocatalysis, ICP - CSIC, Campus UAM-CSIC, Cantoblanco, ZC 28049 Madrid, Spain

ABSTRACT: In this paper is described the optimization of the esterification reaction of butyl acetate synthesis catalyzed by Candida antarctica lipase B (Novozym 435). The reaction parameters temperature, substrate molar ratio, enzyme content, and added water, and their responses measured as conversion yields, were evaluated using central composite design and response surface methodology. The best acid concentration for the reaction without enzyme inactivation was determined to be 0.3 M. The optimal conditions for butyl acetate synthesis were found to be temperature of 40 °C; substrate molar ratio of 3:1 butanol:acetic acid; enzyme content of 7.5% of substrate wt.; added water 0.25% of substrate wt. Under these conditions, over 90% of conversion was obtained in 2.5 h. Enzyme reuse was tested performing three different treatments before each batch: washing the enzyme system with either n-hexane or water, or suspending the immobilized enzyme in water for 24 h. Direct enzyme reuse or washing with water produced a rapid decrease on enzyme activity, while washing with n-hexane allowed enzyme to be reused for 6 reactions cycles keeping around 70% of its activity. This fast and high yield of conversion represents a large improvement to previously reported results.
Palabras clave:
logo de CSIC