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1.
Int J Biol Macromol ; 163: 550-561, 2020 Nov 15.
Article in English | MEDLINE | ID: mdl-32645498

ABSTRACT

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 ≈40% of their initial activity after 48 h of incubation at 50 °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 ≈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 °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.


Subject(s)
Chitosan/chemistry , Enzymes, Immobilized , Eurotiales/enzymology , Lipase/chemistry , Adsorption , Biocatalysis , Chemical Phenomena , Hydrogen-Ion Concentration , Hydrolysis , Hydrophobic and Hydrophilic Interactions , Solvents , Spectroscopy, Fourier Transform Infrared , Thermogravimetry
2.
Enzyme Microb Technol ; 128: 9-21, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31186114

ABSTRACT

Silica has been extracted from rice husks via a simple hydrothermal process and functionalized with triethoxy(octyl)silane -OCTES (Octyl-SiO2) and (3-aminopropyl)triethoxysilane - 3-APTES (Amino-SiO2), with the aim of using it as support to immobilize lipase from Thermomyces lanuginosus (TLL) via adsorption. The supports have been characterized by particle size distribution and elemental analyses, XRD, TGA, SEM, AFM and N2 physisorption so as to confirm their functionalization. Effect of pH, temperature, initial protein loading and contact time on the adsorption process has been systematically evaluated. Maximum immobilized protein loading of 12.3 ± 0.1 mg/g for Amino-SiO2 (5 mM buffer sodium acetate at pH 4.0, 25 °C and initial protein loading of 20 mg/g) and 21.9 ± 0.1 mg/g for Octyl-SiO2 (5 mM buffer sodium acetate at pH 5.0, 25 °C and initial protein loading of 30 mg/g) was observed. However, these biocatalysts presented similar catalytic activity in olive oil emulsion hydrolysis (between 630 and 645 U/g). TLL adsorption was a spontaneous process involving physisorption. Experimental data on Octyl-SiO2 and Amino-SiO2 adsorption were well-fitted to the Langmuir isotherm model. It was also investigated whether these biocatalysts could synthesize cetyl esters via esterification reaction. Thus, it was found that cetyl stearate synthesis required 100-110 min of reaction time to attain maximum conversion percentage (around 94%). Ester productivity of immobilized TLL on Amino-SiO2 was 1.3-3.1 times higher than Octyl-SiO2.


Subject(s)
Adsorption , Enzymes, Immobilized/metabolism , Eurotiales/enzymology , Lipase/metabolism , Hydrogen-Ion Concentration , Hydrolysis , Kinetics , Lipase/isolation & purification , Olive Oil/metabolism , Oryza/chemistry , Silicon Dioxide/isolation & purification , Silicon Dioxide/metabolism , Temperature
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