Abstract: Disclosed is a method of manufacturing a polyurethane filter foam having excellent air permeability, elasticity, and restoring force. In the method of manufacturing the polyurethane filter foam, the cell size of the filter foam is made regular by controlling the pressure by adjusting the diameter of the foaming head of a foaming machine, rather than adding a cell opener, cell irregularity caused by poor dispersion of the cell opener is alleviated, and air permeability, porosity, and compression set are excellent.

Abstract: A display device includes a substrate that includes a display area and a non-display area, a display element layer disposed on the display area of the substrate, an opposing substrate that faces the substrate and the display element layer, a sealing member disposed on the non-display area and that couples the substrate and the opposing substrate, and a filler disposed between the substrate and the opposing substrate. A thickness of the filler varies in the range of 60% to 400% of a thickness of the sealing member.

Abstract: The present invention relates to a method for preparing a protein cage which comprises: a 1st step of preparing an amphiphilic polymer comprising a 1st hydrophobic polymer and a 1st hydrophilic functional group; a 2nd step of preparing a hydrophilic protein comprising a 2nd functional group binding to the 1st functional group; a 3rd step of forming an amphiphilic polymer-protein hybrid by the binding of the 1st functional group and the 2nd functional group, and forming core-shell structured particles comprising a protein shell and an amphiphilic polymer core by the self-assembly of the amphiphilic polymer in a hydrophilic solvent; and a fourth step of removing some or all of the hydrophobic polymer of the core part from the core-shell structured particles.

Abstract: The present invention relates to a method for preparing a protein cage which comprises: a 1st step of preparing an amphiphilic polymer comprising a 1st hydrophobic polymer and a 1st hydrophilic functional group; a 2nd step of preparing a hydrophilic protein comprising a 2nd functional group binding to the 1st functional group; a 3rd step of forming an amphiphilic polymer-protein hybrid by the binding of the 1st functional group and the 2nd functional group, and forming core-shell structured particles comprising a protein shell and an amphiphilic polymer core by the self-assembly of the amphiphilic polymer in a hydrophilic solvent; and a fourth step of removing some or all of the hydrophobic polymer of the core part from the core-shell structured particles.

Abstract: The present invention relates to a process for preparing phenolic polymers utilizing Coprinus cinereus peroxidase. More particularly, the present invention relates to a process for preparing phenolic polymers by polymerizing phenolic monomers with Coprinus cinereus peroxidase instead of using typical peroxidase which essentially requires the use of toxic formalin or peroxidase of plant origin which is very costly and easily deactivated by hydrogen peroxide in the polymerization of phenolic monomers, wherein the polymerization is conducted in the presence of a polar organic solvent under mild reaction conditions of atmospheric temperature and pressure to economically produce desired phenolic polymers having excellent water and chemical resistances with high yield.

Abstract: The present invention relates to a process for preparing phenolic polymers utilizing Coprinus cinereus peroxidase. More particularly, the present invention relates to a process for preparing phenolic polymers by polymerizing phenolic monomers with Coprinus cinereus peroxidase instead of using typical peroxidase which essentially requires the use of toxic formalin or peroxidase of plant origin which is very costly and easily deactivated by hydrogen peroxide in the polymerization of phenolic monomers, wherein the polymerization is conducted in the presence of a polar organic solvent under mild reaction conditions of atmospheric temperature and pressure to economically produce desired phenolic polymers having excellent water and chemical resistances with high yield.

Abstract: The present invention relates to a process for preparing a phenolic polymer using a phenothiazine-based mediator, in particular, to a process for preparing a phenolic polymer via polymerization of phenolic monomers by using a phenothiazine-based mediator in the presence of peroxidase biocatalyst and an oxidant, thereby drastically improving the enzyme reactivity of peroxidase. The phenolic polymers prepared according to the polymerization of this invention maintain unsaturated hydrocarbon groups linked to their side chains, so that they are very useful as a curing resin because they can easily form coatings through radical curing. In addition, the coating formed using the curing resin has an antioxidation effect and a low surface energy, so that they can prevent physical attachment of marine livings. Because the antifouling-causing functional groups are not consumed, the coatings continuously exhibit durability.

Abstract: The present invention provides thermostable phospholipase TA3 and TA13 which are mutants of phospholipase A1 involving the hydrolysis/synthesis of phospholipids, the mutated genes encoding the same, microorganisms transformed with recombinant expression vectors comprising the mutated genes and a process for preparing phospholipase A1 mutants therefrom. The process for preparing phospholipase A1 mutant of the invention comprises the steps of: culturing E. coli strain transformed with a recombinant expression vector comprising a gene coding for phospholipase A1 mutant derived from Serratia sp.; and, isolating and purifying phospholipase A1 mutant from the culture. Since phospholipase A1 mutants of the invention have been improved in terms of thermal stability and enzyme activity as well, they can be practically applied to various biological process, pharmaceutics, cosmetics and food industries.

Abstract: The present invention provides thermostable phospholipase TA3 and TA13 which are mutants of phospholipase A1 involving the hydrolysis/synthesis of phospholipids, the mutated genes encoding the same, microorganisms transformed with recombinant expression vectors comprising the mutated genes and a process for preparing phospholipase A1 mutants therefrom. The process for preparing phospholipase A1 mutant of the invention comprises the steps of: culturing E. coli strain transformed with a recombinant expression vector comprising a gene coding for phospholipase A1 mutant derived from Serratia sp.; and, isolating and purifying phospholipase A1 mutant from the culture. Since phospholipase A1 mutants of the invention have been improved in terms of thermal stability and enzyme activity as well, they can be practically applied to various biological process, pharmaceutics, cosmetics and food industries.