Synthesis of wax ester through triolein alcoholysis:: Choice of the lipase and study of the mechanism

被引:20
作者
Decagny, B
Jan, S
Vuillemard, JC
Sarazin, C
Séguin, JP
Gosselin, C
Barbotin, JN
Ergan, F
机构
[1] Univ Picardie, Fac Sci, Lab Genie Cellulaire, Amiens, France
[2] Univ Laval, Fac Sci Agr & Alimentat, Ctr Rech Sci & Technol Lait, Quebec City, PQ G1K 7P4, Canada
关键词
lipase; screening; alcoholysis; triacylglycerols; wax ester; stearyl oleate; isomerization;
D O I
10.1016/S0141-0229(97)00240-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Eight microbial lipases and one animal tissue lipase were tested for their ability to support alcoholysis between triolein and stearyl alcohol to produce wan ester. The lipases from Alcaligenes sp. and Chromobacterium viscosum were shown to produce the best ester yield (about 53%); however, the reaction was catalyzed in a shorter length of time using the lipase from Alcaligenes sp. (5 h) as compared to the lipase from C. viscosum (200 h). The lipases from Mucor javanicus, Mucor miehei, and Pseudomonas fluorescens showed 35% ester yield within 150 h. The other lipases, i.e., the lipases extracted from porcine pancreas, Candida rugosa, Rhizopus javanicus, and Rhizopus niveus showed only low catalytic activity (less than 20%). The lipase from Alcaligenes sp. was used for further investigations on the mechanism of the reaction. A regioselectivity reward the sn-1,3-positions of the acylglycerols was shown during the first hours of reaction. After 5 h when ester synthesis and triolein consumption stopped the continuous evolution of the concentration of monoolein and diolein isomer forms was ascribed to isomerization reactions. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:578 / 582
页数:5
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