immobilised enzymes Flashcards
what are immobilised enzymes
enzymes that are held in place (taken out of suspension) and not free to mix with the substrate
what are the advantages of using enzymes that have been immobilised
-no mixing with product, lower extraction costs
-easy reuse
-continuous process is easier to set up = no cells needing nutrients, reproducing or releasing waste
-enzymes are surrounded by immobilising matric, making them more stable and protects them, higher temps and wider pH range can be used without denaturing
what are the four methods of enzyme immobilisation
- adsorption
2.binding - entrapment
4.encapsulation
explain adsorption and any problems with the method
-enzymes are adsorbed (attached onto) the surface of an insoluble/ inert support material e.g clay, porous carbon, glass beads and resin
-active site may be slightly distorted by the process, bonding forces are weak so some enzyme may detach and leak into the reaction mixture
explain binding and possible problems with it
-enzymes bound to insoluble/ inert support materials like cellulose or collagen fibres by covalent or ionic bonds
-more expensive, could distort active site but are less likely to detach
explain entrapment and possible problem
enzyme trapped in a matrix e.g. silica gel or a microcapsule
-substrate molecule must be able to diffuse into the entrapment matrix and products diffuse out (only works on relatively small molecules)
explain encapsulation and possible problems
-enzymes may be contained in a partially permeable membrane e.g semi permeable alginate beads
-substrate and product must be small enough to diffuse through the membrane- might limit rate of reaction
what are examples pf immobilised enzymes in biotechnology
-glucose isomerase to convert glucose to fructose
-glucoamylase to convert dextrins to glucose
-lactase for hydrolysis of lactose to glucose and galactose
-penicillin acylase for formation of semisynthetic penicillin which some penicillin resistant organisms are not resistant
-aminoacylase for production of pure samples of L-amino acids