times the volume of eggwhites and stirer for 15 minutes. Silica (SiO2) added as much as 0.851 g and stirer for 10 minutes then add in 20 ml phosphate buffer (NaH2PO4) and stirer for 5 minutes.Lysozyme activity before extraction. We observed that lysozymes heat-treated for 40 min at 100 °C caused a 4.5 log reduction in infectivity of norovirus. Transmission electron microscope analysis showed that virus particles exposed to thermally denatured lysozymes were expanded, compared to the virus before exposure. The main extraction methods of lysozyme include the direct crystallization method [10], ion exchange method [11], ultrafiltration method [12], two-phase system separation method [13], reverse micelle extraction method [14], and affinity membrane chromatography [15]. In this experiment, the aim is to extractlysozyme from duck eggwhites and compare it to the lysozyme from a stock solution of hen lyso-zyme.Determining enzyme kinetics for duck lysozyme Once the extractedlysozyme from duck eggwhite was successfully. A hundred years ago, in 1922, Alexander Fleming discovered lysozyme. Lysozyme (muramidase) is a small alkaline polypeptide whose name is given by its. The mixture of lysozyme and bovine serum albumin was used as a mixture model protein to investigate the adsorption selectivity. The magnetite/isinglass composite was then used for the extraction of lysozyme from eggwhite solutions. fractions of eggwhite proteins by heat treatment in the range 80-95 ° C. Optimal concentration of lysozyme, which inhibits bacterial growth, in the medium. typical for milk products must exceed 2.0 - 2.5 mg / ml. When the conductivity started to rise, the fractions started to be collected. Fractions number 1 to 4 were discarded; fractions number 5 to 11 and the flow-through were loaded on the gel (Fig.

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