1. The Specificity of Oxidase and Kinase Preparations from Pseudomonas fluorescens towards Deoxyfluoromonosaccharides
- Author
-
Hill L, Taylor Nf, and Eisenthal R
- Subjects
chemistry.chemical_element ,Dehydrogenase ,Pseudomonas fluorescens ,Deoxyglucose ,Calcium ,Gluconates ,Glucose Oxidase ,chemistry.chemical_compound ,Drug Stability ,Deoxy Sugars ,Glucose oxidase ,chemistry.chemical_classification ,Oxidase test ,biology ,Phosphotransferases ,Glucosephosphates ,Fluorine ,General Medicine ,biology.organism_classification ,Gluconokinase ,Alcohol Oxidoreductases ,Kinetics ,Enzyme ,chemistry ,Biochemistry ,Spectrophotometry ,biology.protein ,Gluconic acid ,Spectrophotometry, Ultraviolet ,Chromatography, Thin Layer - Abstract
With partially purified enzyme preparations from cell-free extracts of Pseudomonas fluorescens, 3-deoxy-3-fluoro-D-glucose and 3-deoxy-3-fluoro-D-gluconic acid are substrates for glucose oxidase (EC 1.1.3.4.) and gluconate dehydrogenase (EC 1.1.99.3), with Km values 18.2 mM and 11.8 mM, respectively. The same enzymes that oxidize glucose and gluconic acid probably oxidize 3-deoxy-3-fluoro-D-glucose and 3-deoxy-3-fluoro-D-gluconic acid. The latter fluorinated carbohydrates and the presumed formation of 3-deoxy-3-fluoro-2-keto-D-gluconic acid, which has been isolated as a calcium salt and characterized, are not substrates for gluconokinase (EC 2.7.1.12). Both 3-deoxy-3-fluoro-D-glucose and 3-deoxy-3-fluoro-D-gluconic acid act as competitive inhibitors of this enzyme preparation for gluconate, with Ki values 47.5 mM and 14.8 mM, respectively.
- Published
- 1975