4.0 Article

Production of structured lipids by acidolysis with immobilized Rhizomucor miehei lipases: Selection of suitable reaction conditions

Journal

JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
Volume 76, Issue -, Pages 106-115

Publisher

ELSEVIER
DOI: 10.1016/j.molcatb.2011.11.022

Keywords

Acidolysis; Structured lipids; Sunflower oil; Saturated fatty acids; Rhizomucor miehei lipase

Funding

  1. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET)
  2. Agenda Nacional de Promocion Cientifica y Tecnologica (ANPCyT)
  3. Universidad Nacional del Sur (UNS) in Argentina

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Enzymatic modification of vegetable oils can be used to produce plastic fat or structured lipids (SL) avoiding the generation of trans fatty acids. Biocatalysts previously prepared by immobilization of Rhizomucor miehei lipases onto alkylated chitosan microspheres were used to synthesize SL by acidolysis reaction of sunflower oil and palmitic-stearic acids mixture. Effects of some reaction parameters, substrate molar ratio (SR), amount of biocatalyst (E) and amount of solvent (H), over selected response variables were analyzed by applying an incomplete factorial design of three factors with three levels (Box-Behnken). Responses were selected to evaluate not only the development of desired TAG but also the yield and quality of obtained products, through by-products and undesired trisaturated lipids quantification. The analysis of variable effects showed that E was the most significant factor on each analyzed response. Multi-response optimization with restrictions from practical considerations revealed that maximum saturated fatty acids composition in glycerides of the SL (38.6%) is obtained when SR = 3, E = 0.34 g and H = 3.2 ml are used. Under these conditions, a change in the composition of the desired TAG group (monounsaturated TAG) from 2.5% in the original oil to 33.9% in the final product was achieved. On the other hand, time and temperature behavior studies showed that generation of trisaturated triacylglycerols and by-products were favored mainly by increasing temperature. After 12 h of reaction, overall hydrolysis and esterification reactions rates were comparable. However, TAG distribution continued changing. (C) 2011 Elsevier B.V. All rights reserved.

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