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US 4,172,763 AGranted
Preparation of high purity xanthine oxidase from bovine milk
AssigneeUniversity of Delaware
InventorJohn P. Zikakis
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AssigneeUniversity of Delaware
InventorJohn P. Zikakis
Estimating the term…
Bovine milk xanthine oxidase, referred to herein as XO, is isolated and purified from raw whole milk by a streamline method without the use of proteolytic and lipolytic enzymes, butanol, or other organic solvents. Sodium salicylate, ethylenediaminetetraacetate (EDTA), and a 0.2 M phosphate buffer are added to fresh milk. After incubation at 40.degree.-45.degree. C. for 105 min., the mixture is adjusted to 1-2% with Triton X-100 and allowed to incubate for 15 min. The mixture is cooled to 4.degree. C., followed by a 2-step fractionation of the proteins with ammonium sulfate. The crude enzyme is isolated as a red-brown precipitate which is dissolved in 0.1 M Tris/CaCL.sub.2 buffer and stored for from 12 to 168 hours at -20.degree. C. The isolated enzyme is purified by column chromatography (Sephadex G-75, Sephacryl S-200, Sepharose 6B, and Sephadex G-75). The final stage of purification is accomplished by passing the enzyme preparation through a DEAE-Sephadex A-50 column in a continuous linear salt gradient from 0.005 M to 0.1 M pyrophosphate buffer. The purified enzyme is not denatured and has, on the average, a constant E.sub.280 /E.sub.450 ratio of 4.1, and one symmetric peak by gel chromatography. Analysis by polyacrylamide disc gel electrophoresis demonstrates a single band, while commercially available XO shows 7-14 bands, only one of which contains XO activity (the rest being impurities). The average yield of the final product is about 21% which is 110% higher than the yield of less pure XO obtained using the best prior art.
A process for the isolation and purification of xanthine oxidase from milk which comprises first incubating the milk in the presence of sodium salicylate, ethylenediaminetetraacetate, and a phospate buffer and then adding a non-ionic detergent to the milk and allowing it to incubate for a shorter period of time, reducing the temperature to stop incubation and adding sufficient ammonium sulfate to precipitate the caseins but not the xanthine oxidase, separating the caseins and other solids and adding sufficient ammonium sulfate to the supernatant liquid to precipitate the xanthine oxidase, separating the red-brown precipitate and dissolving same in a Tris/CaCl.sub.2 buffer followed by storing the solution at freezing or below for at least 15 hours to effect further separation of casein upon thawing, separating the supernatant liquid containing the xanthine oxidase and filtering said liquid with an ultrafilter which will retain molecules of 50,000 daltons and greater, applying the concentrated retained material on an equilibrated chromatographic column, eluting the column with a buffer solution, collecting the eluent in multiple fractions, testing the fractions for xanthine oxidase activity, combining the samples that show acceptable activity, and continuing this process with chromatographic columns of varying characteristics until the desired xanthine oxidase purity is obtained.
In a process of recovering xanthine oxidase from milk wherein milk is first incubated in the presence of sodium salicylate, ethylenediaminetetraacetate and phosphate buffer, the improvement comprises adding a non-ionic detergent to the milk after the first stage of incubation and further allowing it to incubate for a shorter period of time before reducing its temperature.
In a process of recovering xanthine oxidase from the crude mixture remaining after the removal of most of the casein through long-term precipitation at -20.degree. C. and centrifugation, the improvement comprises filtering with an ultrafilter which will retain molecules of 50,000 daltons and greater, applying the concentrated retained material on an equilibrated chromatographic column, eluting the column with a buffer solution, collecting the eluent in multiple fractions, testing the fractions for xanthine oxidase activity, combining the samples that show acceptable activity, and continuing this process with chromatographic columns of varying characteristics until the desired xanthine oxidase purity is obtained.
Dependencies are inferred from the claim text.