Lipase immobilization on hyroxypropyl methyl cellulose support and its applications for chemo-selective synthesis of β-amino ester compounds

被引:26
作者
Badgujar, Kirtikumar C. [1 ]
Bhanage, Bhalchandra M. [1 ]
机构
[1] Inst Chem Technol, Dept Chem, Bombay 400019, Maharashtra, India
关键词
Lipase; Immobilization; Ester compounds; Biocatalysis; Improved activity; AZA-MICHAEL REACTION; ENHANCED BIOCATALYTIC ACTIVITY; PSEUDOMONAS-CEPACIA LIPASE; ENANTIOSELECTIVE SYNTHESIS; LEVULINIC ACID; ORGANIC MEDIA; CHEMOSELECTIVITY; MATRIX; TRANSESTERIFICATION; PROMISCUITY;
D O I
10.1016/j.procbio.2016.07.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present study carried out the synthesis of beta-amino ester compounds using lipase immobilized on hyroxypropyl methyl cellulose (HMC) support. Initially various lipases (biocatalysts) from different origin were immobilized and subsequently screened to obtain the robust biocatalyst. The lipase Pseudomonas fluorescence (PFL) immobilized on HMC was displayed highest lipase activity, protein content and retention of activity. The physical and biochemical characterization verified immobilization of lipase PFL on the HMC support. This immobilized biocatalyst HMC:PFL (3.5:1) was successfully applied for the practical biocatalytic applications to synthesize variety of beta-amino esters. Various eight reaction parameters were optimized in details to achieve the maximum yield and chemo-selectively. The developed biocatalytic protocol was successfully applied to synthesize different industrially important beta-amino esters compounds (21 substrates) with an excellent yield (>90%) and remarkable chemo selectivity (>94%). Interestingly, the immobilized HMC:PFL lipase showed 2.1-2.5 folds higher bio-catalytic activity and five times recyclability as compared to the free PFL. The plausible mechanism for lipase catalyzed synthesis of beta-amino ester compounds was also proposed. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1420 / 1433
页数:14
相关论文
共 67 条