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Optimized butyl butyrate synthesis catalyzed by Thermomyces lanuginosus lipase

Authors

  • Andréa B. Martins,

    1. Biocatalysis and Enzyme Technology Lab, Institute of Food Science and Technology, Federal University of Rio Grande do Sul State, Rio Grande do Sul, Brazil
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  • John L. R. Friedrich,

    1. Biocatalysis and Enzyme Technology Lab, Institute of Food Science and Technology, Federal University of Rio Grande do Sul State, Rio Grande do Sul, Brazil
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  • Rafael C. Rodrigues,

    Corresponding author
    1. Biocatalysis and Enzyme Technology Lab, Institute of Food Science and Technology, Federal University of Rio Grande do Sul State, Rio Grande do Sul, Brazil
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  • Cristina Garcia-Galan,

    1. Dept. of Biocatalysis, ICP – CSIC, Campus UAM-CSIC, Madrid, Spain
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  • Roberto Fernandez-Lafuente,

    1. Dept. of Biocatalysis, ICP – CSIC, Campus UAM-CSIC, Madrid, Spain
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  • Marco A. Z. Ayub

    1. Biochemical Engineering Lab (BiotecLab), Institute of Food Science and Technology, Federal University of Rio Grande do Sul State, Rio Grande do Sul, Brazil
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Abstract

Butyl butyrate is an ester present in pineapple flavor, which is very important for the food and beverages industries. In this work, the optimization of the reaction of butyl butyrate synthesis catalyzed by the immobilized lipase Lipozyme TL-IM was performed. n-Hexane was selected as the most appropriate solvent. Other reaction parameters such as temperature, substrate molar ratio, biocatalyst content and added water, and their responses measured as yield, were evaluated using a fractional factorial design, followed by a central composite design (CCD) and response surface methodology. In the fractional design 24–1, the four variables were tested and temperature and biocatalyst content were statistically significant and then used for optimization on CCD. The optimal conditions for butyl butyrate synthesis were found to be 48°C; substrate molar ratio 3:1 (butanol:butyric acid); biocatalyst content of 40% of acid mass. Under these conditions, over 90% of yield was obtained in 2 h. Enzyme reuse was tested by washing the biocatalyst with n-hexane or by direct reuse. The direct reuse produced a rapid decrease on enzyme activity, while washing with n-hexane allowed reusing the enzyme for five reactions cycles keeping approximately 85% of its activity. © 2013 American Institute of Chemical Engineers Biotechnol. Prog., 29:1416–1421, 2013

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