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Enzymatic Synthesizing of Phytosterol Oleic Esters

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Abstract

A method of synthesizing the phytosterol esters from oleic acid and sterols was studied, using immobilized lipase Candida sp. 99–125 as catalyst. Molar ratio (oleic acid/phytosterols), temperature, reaction period, organic solvents, catalyst, and silica-gel drier were optimized, and the result showed that 93.4% of the sterols had been esterified under the optimal synthetic condition: the molar ratio of oleic acid/phytosterol is 1:1 in 10 mL iso-octane, immobilized lipase (w, 140% of the sterols), incubated in an orbital shaker (200 rpm) at a temperature of 45 °C for 24 h. The immobilized lipase could be reused for at least 13 times with limited loss of esterification activity. The conversion still maintained up to 86.6%. Hence, this developed process for synthesizing phytosterol esters could be considered as simple and low-energy consumption compared to existing chemical processes.

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Correspondence to Tianwei Tan.

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Pan, X., Chen, B., Wang, J. et al. Enzymatic Synthesizing of Phytosterol Oleic Esters. Appl Biochem Biotechnol 168, 68–77 (2012). https://doi.org/10.1007/s12010-011-9324-x

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  • DOI: https://doi.org/10.1007/s12010-011-9324-x

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