4.7 Article

A novel and controllable method for simultaneous preparation of human milk fat substitutes (OPL, OPO and LPL): two-step enzymatic ethanolysis-esterification strategy

Journal

FOOD RESEARCH INTERNATIONAL
Volume 163, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.foodres.2022.112168

Keywords

Human milk fat substitutes (HMFS); Structured triacylglycerol; Immobilization enzyme; Candida sp; lipase (CSL); 2-monopalmitoylglycerol; Acyl migration

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This paper proposes a novel and effective two-step ethanolysis-esterification strategy for the controllable and simultaneous preparation of 1-oleoyl-2-palmitoyl-3-linoleoylglycerol (OPL), 1,3-dioleoyl-2-palmitoyl-glycerol (OPO), and 1,3-dilinoleoyl-2-palmitoyl-glycerol (LPL) with adjustable proportions. Enzymatic ethanolysis of fractionated palm stearin yields 2-monopalmitoylglycerol (79.4 +/- 0.6 %) with over 91.0 % purity. Using immobilized Candida sp. lipase (CSL) on octyl-functionalized ordered mesoporous silica (OMS-C8), 2-monopalmitoylglycerol is re-esterified with oleic acid and linoleic acid to produce OPL, OPO, and LPL simultaneously.
A novel and effective approach based on the two-step ethanolysis-esterification strategy was proposed for the controllable and simultaneous preparation of 1-oleoyl-2-palmitoyl-3-linoleoylglycerol (OPL), 1,3-dioleoyl-2-palmitoyl-glycerol (OPO) and 1,3-dilinoleoyl-2-palmitoyl-glycerol (LPL) with adjustable proportions. Enzymatic ethanolysis of fractionated palm stearin was carried out to yield 2-monopalmitoylglycerol (79.4 +/- 0.6 %) with over 91.0 % purity at the optimal conditions. The immobilized Candida sp. lipase (CSL) on octyl-functionalized ordered mesoporous silica (OMS-C8) was applied to re-esterify 2-monopalmitoylglycerol with oleic acid and linoleic acid for the simultaneous production of OPL, OPO, and LPL. The total content in the final products was 81.5 %, with 91.3 % of palmitic acid (PA) content at the sn-2 position. Besides, OPL/OPO/LPL was conveniently prepared with suitable proportions for worldwide infants by adjusting the ratio of acyl donors. This paper provides a novel and effective two-step ethanolysis-esterification strategy for the development of human milk fat substitutes (HMFS).

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