Optimization of HPLC technique for determining catalytic parameters of D-amino acid oxidase on cephalosporin C

被引:1
|
作者
Golubev I.V. [1 ,2 ]
Komarova N.V. [2 ,3 ]
Skirgello O.E. [1 ,2 ]
Osipova T.A. [1 ]
Tishkov V.I. [1 ,2 ,3 ]
机构
[1] Department of Chemistry, Moscow State University, Moscow
[2] Innovations and High Technologies, MSU Ltd., Moscow
[3] Bach Institute of Biochemistry, Russian Academy of Sciences, Moscow
关键词
catalytic parameters; cephalosporin C; D-amino acid oxidase; high performance liquid chromatography; Trigonopsis variabilis;
D O I
10.3103/S0027131414020035
中图分类号
学科分类号
摘要
Approximately half of cephalosporin antibiotics of different generations are produced from 7-aminocephalosporanic acid, which to date is prepared by organic synthesis. Instead of organic synthesis, a two-step enzymatic process is gradually being developed. The first step is enzymatic oxidation of natural antibiotic cephalosporin C by D-amino acid oxidase (DAAO). Yeast enzymes are used for this purpose due to the highest activity on cephalosporin C. The standard technique of determining the activity of D-amino acid oxidase is based on determining the concentration of released hydrogen peroxide using horseradish peroxidase. During cephalosporin C oxidation, hydrogen peroxide is involved in the spontaneous nonenzymatic reaction with the intermediate product. Thus, monitoring the substrate consumption with high-performance liquid chromatography (HPLC) is the most correct way to determine the activity. In this paper, we have optimized the HPLC technique of determining the cephalosporin C concentration during its oxidation with D-amino acid oxidase in the reaction mixture. Using the optimized technique, we have determined the catalytic parameters for wild-type and mutant D-amino acid oxidase on cephalosporin C. © 2014 Allerton Press, Inc.
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页码:68 / 72
页数:4
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