Amperometric trienzyme ATP biosensors based on the coimmobilization of salicylate hydroxylase, glucose-6-phosphate dehydrogenase, and hexokinase
| Autor: | Reinhard Renneberg, Yue Cui, John P. Barford |
|---|---|
| Rok vydání: | 2008 |
| Předmět: |
Hexokinase
Chemistry Metals and Alloys Dehydrogenase Condensed Matter Physics Phosphate Amperometry Surfaces Coatings and Films Electronic Optical and Magnetic Materials law.invention chemistry.chemical_compound Biochemistry law Materials Chemistry Glucose-6-phosphate dehydrogenase NAD+ kinase Electrical and Electronic Engineering Instrumentation Clark electrode Biosensor |
| Zdroj: | Sensors and Actuators B: Chemical. 132:1-4 |
| ISSN: | 0925-4005 |
| DOI: | 10.1016/j.snb.2008.01.001 |
| Popis: | Two types of amperometric ATP biosensors were developed by using the coimmobilization of salicylate hydroxylase (SHL, EC 1.14.13.1), glucose-6-phosphate dehydrogenase (G6PDH, EC1.1.1.49), and hexokinase (HEX, EC 2.7.1.1) on a Clark-type oxygen electrode and on a screen-printed electrode. The principles of the determination schemes are as follows: HEX transfers the phosphate group from ATP to glucose to form glucose-6-phosphate. G6PDH catalyzes the specific dehydrogenation of glucose-6-phosphate by consuming NAD+. The product, NADH initiates the irreversible decarboxylation and hydroxylation of salicylate by SHL to consume dissolved oxygen and generate catechol. This results in a detectable signal on a Clark-type electrode due to the SHL-enzymatic consumption of oxygen, or a detectable signal on a screen-printed electrode due to the SHL-enzymatic generation of catechol in the measurement of ATP. Both sensors show high performance characteristics with broad detection ranges, short measuring times, and good specificities. |
| Databáze: | OpenAIRE |
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