4.0 Article

Biosynthesis of ethyl caproate and other short ethyl esters catalyzed by cutinase in organic solvent

Journal

JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
Volume 60, Issue 3-4, Pages 178-185

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcatb.2009.05.004

Keywords

Ethyl caproate; Short chain ethyl esters; Cutinase; Organic solvent; Iso-octane

Funding

  1. Fundacao para a Ciencia e a Tecnologia (Portugal) [SFRH/BD/24703/2005]
  2. Fundação para a Ciência e a Tecnologia [SFRH/BD/24703/2005] Funding Source: FCT

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The main objective of this work was to study the enzymatic synthesis of short chain ethyl esters, a group of relevant aroma molecules, by Fusarium solani pisi cutinase in an organic solvent media (iso-octane), and to assess the influence of different parameters on the reaction yield. Cutinase displayed high initial esterification rates in iso-octane. which amounted to 1.15 mu mol min(-1) mg(-1) for ethyl butyrate (C-4 acid chain) and 1.06 mu mol min(-1) mg(-1) for ethyl valerate (C-S acid chain). High product yields, 84% for ethyl butyrate and 96% for ethyl valerate, were observed after 6 h of reaction, for an initial equimolar concentration of substrates (0.1 M). The highest product yield (97%) was observed for ethyl caproate (C-6) synthesis, a compound which is a part of natural apple and pineapple flavour, for an alcohol:acid molar ratio of 2 (0.2 M ethanol concentration). Cutinase affinity for short chain length carboxylic acids (C-4-C-6) in ester synthesis in iso-octane confirmed previous observations in reversed micellar system. (C) 2009 Elsevier B.V. All rights reserved.

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