Very stable silica-gel-bound laccase biocatalysts for the selective oxidation in continuous systems.

Cerrena unicolor laccase was immobilized by adsorption and covalent bonds formation on silica-gel carriers, functionalized with different organosilanes and surface densities. The effects of protein concentration, pH value of the coupling mixture and the enzyme purity on immobilization efficiency of the best carrier, moderately modified (0.75 mmol/g carrier) with 3-aminopropyltriethoxysilane were investigated. Activity of the best biocatalysts, expressed in ABTS oxidation, was 4028 U/mL of the carrier or 3530 U/mg of bound protein. Properties of immobilized laccase were determined to find excellent thermal stability improvement; t(1/2) for freely suspended enzyme was 2-3 min at 80 degrees C, whereas after immobilization over 100 min. Kinetic experiments in both batch and packed-bed reactors gave only four times lower k(cat)/K(m) value than for the native enzyme. A packed-bed reactor with silica-gel-bound laccase beads appeared to be very efficient in ABTS oxidation and its exceptional potentials were shown in the continuous decolorization of indigo carmine for 18 days without loss in activity. This system offers perfect ability to degrade recalcitrant dyes, but we can also envisage its use, with ABTS acting as a mediator, in regeneration of nicotinamide cofactors.

Effective purification of Cerrena unicolor laccase using microfiltration, ultrafiltration and acetone precipitation.

Microfiltration followed by concentration and diafiltration on ultrafiltration membranes (Biomax-100, Biomax-10 and Ultracel-10) was used to recover extracellular laccase (EC 1.10.3.2) from culture broth of wood-rotting fungus Cerrena unicolor. Feed, permeate, retentate and membrane wash-out solutions were analysed for the presence of laccase, proteases, protein and brown impurities. An easy, cheap and short-term procedure was proposed to obtain retentates with low yields of total proteins (less than 14%), proteases activity (less than 15%) and brown impurities (from 2% to 29%) with a simultaneous laccase recovery above 73%. The degree of laccase purification varied from 6.7 to 11.0 and depended on the type of membrane used and content of brown pigments in the feed. Subsequent protein precipitation with cold acetone increased the degree of purification about twice and reduced proteases and brown impurities to some extent. Ultracel-10 membrane was recommended as the best solution to prevent fouling of membranes and to obtain laccase-enriched fraction with a very low content of proteases and brown pigments.

Laccase immobilization on the tailored cellulose-based Granocel carriers.

Extracellular laccase produced by Cerrena unicolor was immobilized by adsorption or covalent bonds formation on the cellulose-based carrier Granocel. Immobilization was optimized by changing the anchor groups and the methods of activation/immobilization. On the base of measured activity and stability of immobilized preparations, the covalent method was selected. It was shown that coupling of the enzyme to the carrier via divinyl sulfone or glutaraldehyde yielded an enzyme-carrier preparation of high activity and storage stability. Further optimization of the carrier's superstructure consisted in changing pore diameters and amount of functional groups on the carriers surface. Three-fold higher activity was noted when the enzyme was immobilized on NH2-modified Granocel with the highest size exclusion limit and amino group content. Relatively low products sorption was observed on the carrier surface. The effects of protein concentration and pH-value of the coupling mixture on immobilization efficiency were evaluated also.