Esterification of hydrophobic substrates by lipase in the cyclodextrin induced emulsion reaction system

被引:18
|
作者
Shin, HD [1 ]
Kim, JH [1 ]
Kim, TK [1 ]
Kim, SH [1 ]
Lee, YH [1 ]
机构
[1] Kyungpook Natl Univ, Coll Nat Sci, Dept Genet Engn, Taegu 702701, South Korea
关键词
esterification; lipase; hydrophobic substrates; oleic acid; n-butanol; cyclodextrin; CD-induced emulsion reaction system;
D O I
10.1016/S0141-0229(02)00025-X
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
Cyclodextrin (CD), a doughnut-shaped molecule having a hydrophilic surface and hydrophobic interior, can form inclusion complexes with various hydrophobic guest molecules inducing them into the emulsion state. The CD-induced emulsion reaction system was applied to the esterification between the hydrophobic oleic acid as the carboxylic acid and n-butanol as the alcohol catalyzed by lipase. The rate and yield were substantially increased in the CD-induced emulsion reaction system. The optimal reaction condition and the kinetic constants of the esterification reaction were determined. The enhancing mechanism was investigated through comparing the microscopic observation of the reaction mixtures, the inclusion complex formability, and the distribution of substrates, product and lipase at aqueous phase and CD-induced water immiscible phase in the CD-induced emulsion reaction system. The increase seems to have been caused by three reasons, the increased accessibility of lipase due to the emulsion formation, the shift of the equilibrium to the product formation side through the decrement of the affinity of butyl oleate with lipase, and the activation of lipase adsorbed on interface of oil-droplets in CD-induced water immiscible phase. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:835 / 842
页数:8
相关论文
共 50 条
  • [21] Lipase immobilized on poly(VP-co-HEMA) hydrogel for esterification reaction
    Basri, M
    Samsudin, S
    Bin Ahmad, M
    Razak, CNA
    Salleh, AB
    APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 1999, 81 (03) : 205 - 217
  • [22] Effect of reductive alkylation of Candida rugosa lipase on its enantioselective esterification reaction
    Basri, M
    Th'ng, BL
    Razak, CNA
    Salleh, AB
    ENZYME ENGINEERING XIV, 1998, 864 : 192 - 197
  • [24] Immobilization of lipase from Candida rugosa on layered double hydroxides for esterification reaction
    Mohd Basyaruddin A. Rahman
    Mahiran Basri
    Mohd Zobir Hussein
    Raja Nor Zaliha A. Rahman
    Dara Hatira Zainol
    Abu Bakar Salleh
    Applied Biochemistry and Biotechnology, 2004, 118 : 313 - 320
  • [25] Kinetics of the esterification reaction catalyzed by lipase in W/O microemulsions of alkyl polyglucoside
    Chai, JL
    Wang, SQ
    Li, GZ
    Xu, Q
    Gao, YH
    CHINESE CHEMICAL LETTERS, 2004, 15 (06) : 699 - 702
  • [26] The role of silica gel in lipase-catalyzed esterification reactions of high-polar substrates
    Castillo, E
    Dossat, V
    Marty, A
    Condoret, JS
    Combes, D
    JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1997, 74 (02) : 77 - 85
  • [27] Role of silica gel in lipase-catalyzed esterification reactions of high-polar substrates
    Castillo, Edmundo
    Dossat, Valerie
    Marty, Alain
    Condoret, J.Stephane
    Combes, Didier
    JAOCS, Journal of the American Oil Chemists' Society, 1997, 74 (02): : 77 - 85
  • [28] Conjugation of Candida rugosa lipase with hydrophobic polymer improves esterification activity of vitamin E in nonaqueous solvent
    Hou, Xiaoyun
    Shi, Qinghong
    CHINESE JOURNAL OF CHEMICAL ENGINEERING, 2023, 62 : 182 - 191
  • [29] Kinetic studies on the Rhizomucor miehei lipase catalyzed esterification reaction of oleic acid with 1-butanol in a biphasic system
    Kraai, G. N.
    Winkelman, J. G. M.
    de Vries, J. G.
    Heeres, H. J.
    BIOCHEMICAL ENGINEERING JOURNAL, 2008, 41 (01) : 87 - 94
  • [30] Conjugation of Candida rugosa lipase with hydrophobic polymer improves esterification activity of vitamin E in nonaqueous solvent
    Xiaoyun Hou
    Qinghong Shi
    Chinese Journal of Chemical Engineering, 2023, 62 (10) : 182 - 191