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Abstract: Nonwoven fabrics of polypropylene (PP), polyethylene terephthalate (PET) and viscose fiber were used as novel and inexpensive support membranes for the immobilization of lipase. The use of a co-solvent during the immobilization process improved the activity of the coupled protein and the operational stability of PP and PET membranes. Covalent methods of immobilization caused the support membranes to become fragile and the lipase was easily deactivated. A hydrophobic treatment improved the protein-coupled content of silk cotton, viscose and PET surfaces more than threefold. Viscose prepared with the hydrophobic treatment could be reused up to 44 times and retained a static water contact angle of 131.8°. The initial rate of esterification remained high even when the amount of added water was increased to 10%. In a model application reaction of oleic acid and ethanol with 8% (v/v) added water, the acid conversion rate of post-hydrophobic treated immobilized lipase improved by at least 10% in each of five batches. These results suggest that a hydrophobic surface results in a lower amount of adsorbed water on the support membrane and provides a more suitable microenvironment for the enzymes. Nonwoven viscose could be a potential enzyme immobilization matrix for industrial processes. [Copyright &y& Elsevier]

In this work, phytosterol ester was synthesized using Yarrowia lipolytica lipase Ylip2 that had been immobilized on inorganic support in a solvent-free system and reacted in a computer-aided water activity controlled bioreactor. The immobilization of Ylip2 on celite led to a remarkable increase in the phytosterol conversion compared to that of free lipase. An investigation of the reaction conditions were oleic acid as the fatty acid variety, 10,000 U/g substrate, and a temperature of 50 °C for phytosterol ester synthesis. Controlling of the water activity at a set point was accomplished by the introduction of dry air through the reaction medium at a digital feedback controlled flow rate. For the esterification of phytosterol ester, a low (15%) water activity resulted in a considerable improvement in phytosterol conversion (91.1%) as well as a decreased reaction time (78 h). Furthermore, Ylip2 lipase immobilized on celite retained 90% esterification activity for the synthesis of phytosterol oleate after reused 8 cycles, while free lipase was only viable for 5 batches with 90% esterification activity remained. Finally, the phytosterol oleate space time yield increased from 1.65 g/L/h with free lipase to 2.53 g/L/h with immobilized lipase. These results illustrate that the immobilized Yarrowia lipolytica lipase Ylip2 in a water activity controlled reactor has great potential for the application in phytosterol esters synthesis. [ABSTRACT FROM AUTHOR]

We have developed an improved and effective method to immobilize Yarrowia lipolytica lipase Lip2 (YLIP2) on an epoxy poly-(glycidylmethacrylate-triallyisocyanurate-ethyleneglycoldimethacrylate) (P GMA-TAIC-EGDMA ) support structure with or without amine or/and protein modifications. Our results show that there is an increase in the activity of the immobilized lipase on n-butylamine (BA) modified support (420 U/g support) and the biocompatible gelatin modified support (600 U/g support) when compared to the support without modification (240 U/g support). To further study the influences of BA and gelatin modification on the activity of the immobilized lipase, gelatin and BA were concurrently used to decorate the support structure. Lipase immobilized on 2% BA/gelatin (1:1) modified support obtained the highest activity (1180 U/g support), which was five-fold higher than that on a native support structure. These results suggest that the activity of a support-immobilized lipase depends on the support surface properties and a moderate support surface micro-environment was crucial for elevated activity. Collectively, these data show that a combined gelatin and BA modification regulates the support surface more suitable for immobilizing YLIP2. [ABSTRACT FROM AUTHOR]

Highlights: [•] A simple, efficient immobilization protocol on polyurethane foam was developed. [•] Polyethyleneimine (PEI) was used to regulate the micro-environment. [•] Immobilized lipase exhibited a long operational stability in esterification system. [Copyright &y& Elsevier]