Improved immobilization of lipase from Thermomyces lanuginosus on a new chitosan-based heterofunctional support: Mixed ion exchange plus hydrophobic interactions

被引:59
作者
Okura, Nicole S. [1 ,2 ]
Sabi, Guilherme J. [2 ]
Crivellenti, Marcela C. [2 ]
Gomes, Raphael A. B. [2 ]
Fernandez-Lafuente, Roberto [3 ]
Mendes, Adriano A. [1 ,2 ]
机构
[1] Univ Fed Alfenas, Grad Program Biotechnol, BR-37130001 Alfenas, MG, Brazil
[2] Univ Fed Alfenas, Inst Chem, BR-37130001 Alfenas, MG, Brazil
[3] CSIC, Dept Biocatalisis, Inst Catalisis, Campus UAM CSIC, E-28049 Madrid, Spain
关键词
Heterofunctional supports; Chitosan-based hydrogels; Lipase; Catalytic properties; COVALENT IMMOBILIZATION; ENZYME IMMOBILIZATION; REVERSIBLE IMMOBILIZATION; INDUSTRIAL APPLICATIONS; BIODIESEL PRODUCTION; ACTIVATED SUPPORTS; MICROBIAL LIPASES; GRAPHENE OXIDE; AGAROSE BEADS; ALKYL ESTERS;
D O I
10.1016/j.ijbiomac.2020.07.021
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
In this study, a new mixed heterofunctional support (Chit-GA-Gly) has been prepared by sequential activation of chitosan hydrogel (Chit) with glutaraldehyde (GA) and further functionalization with glycine (Gly). The immobilization of the lipase from Thermomyces lanuginosus (TLL) on this support was compared with that on GA-activated Chit hydrogel (Chit-GA). The supports have been characterized by FT-IR, zeta potential and TG analyses. A similar maximum lipase loading of 53-55 mg per gram of support has been obtained for both supports. Both biocatalysts retained approximate to 40% of their initial activity after 48 h of incubation at 50 degrees C in heptane, toluene or iso-octane. The immobilization of TLL on Chit-GA proceeded via preferential covalent attachment (95%) and a combined ion exchange (cationic and anionic) and hydrophobic adsorption was observed using Chit-GA-Gly. TLL immobilized on Chit-GA-Gly was approximate to 4-times more active than when immobilized on Chit-GA in both olive oil emulsion hydrolysis and alkyl palmitate synthesis via esterification. Isoamyl palmitate synthesis in iso-octane at 50 degrees C using this new biocatalyst gave a maximum acid conversion of 85% after 90 min of reaction. After nine consecutive esterification batches, the biocatalyst retained around 40% of its initial activity. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:550 / 561
页数:12
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