USA Inc. (NJ, USA) and the mutant B11 (T30V, I94V) was generated by directed evolution as previously described [10]. ... ">

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Yeast surface display for the expression, purification and characterization of wild-type and B11 mutant glucose oxidases.

Protein Expr Purif.. 2013-06;  89(2):175 - 80
Blazic M, Kovacevic G, Prodanovic O, Ostafe R, Gavrovic-Jankulovic M, Fischer R, Prodanovic R. Center for Chemistry IHTM, University of Belgrade, Njegoševa 12, 11001 Belgrade, Serbia.
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摘要

Glucose oxidase (GOx) catalyzes the oxidation of glucose to form gluconic acid and hydrogen peroxide, a reaction with important applications in food preservation, the manufacture of cosmetics and pharmaceuticals, and the development of glucose monitoring devices and biofuel cells. We expressed Aspergillus niger wild type GOx and the B11 mutant, which has twice the activity of the wild type enzyme at pH 5.5, as C-terminal fusions with the Saccharomyces cerevisiae Aga2 protein, allowing the fusion proteins to be displayed on the surface of yeast EBY100 cells. After expression, we extracted the proteins from the yeast cell wall and purified them by ion-exchange chromatography and ultrafiltration. This produced a b... More

关键词

Saccharomyces cerevisiae; Glucose oxidase; Directed evolution; High throughput screening; Chimera
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