Enzyme electrode

• US 20030178998A1
• Filed: 02/11/2003
• Published: 09/25/2003
• Est. Priority Date: 09/25/2000
• Status: Active Grant

• Current Assignee: Asahi Kasei Kabushiki Kaisha
• Original Assignee: Asahi Kasei Kabushiki Kaisha
• Inventors: Ikura, Yoshiaki, Nomura, Masayuki
• Granted Patent: US 7,169,273 B2
• Time in Patent Office: Days
• US Class Current: 324/448
• CPC Class Codes: C12Q 1/005 involving specific analytes or enzymes including groups of enzymes, e.g. oxydases; C12Q1/004 takes precedence
• CPC Class Codes: C12Q 1/008 for determining co-enzymes or co-factors, e.g. NAD, ATP
• CPC Class Codes: C12Q 1/32 involving dehydrogenase

Abstract

Disclosed is an enzyme electrode comprising an electrode system comprising an insulating substrate having formed thereon a working electrode, a counter electrode and optionally a reference electrode, and a reaction layer formed on the electrode system, wherein the reaction layer comprises diaphorase (DI), 12α-hydroxysteroid dehydrogenase (12α-HSD) and nicotinamide adenine dinucleotide synthetase (NADS), at least a portion of the reaction layer being superposed on the working electrode, wherein the DI, 12α-HSD and NADS contained in the reaction layer are immobilized on the surface of the working electrode, so that a compound generated in the reaction layer can reach the surface of the working electrode. Also disclosed are a method for and a system for determining the concentration of adenosine triphosphate (ATP) in a sample by using the above-mentioned enzyme electrode.

Claims

1. An enzyme electrode comprising:

(a) an electrode system comprising an insulating substrate having formed thereon a working electrode, a counter electrode and optionally a reference electrode; and

(b) a reaction layer formed on said electrode system, wherein said reaction layer comprises diaphorase (DI), 12α

-hydroxysteroid dehydrogenase (12α

-HSD) and nicotinamide adenine dinucleotide synthetase (NADS),

at least a portion of said reaction layer being superposed on said working electrode, wherein the DI, 12α

-HSD and NADS contained in said portion of the reaction layer are immobilized on the surface of said working electrode, so that a compound generated in said reaction layer can reach the surface of said working electrode.

2. The enzyme electrode according to claim 1, which further comprises a hydrophilic polymer layer, said hydrophilic polymer layer being interposed between said working electrode and said reaction layer and being in contact with both of said working electrode and said reaction layer.

3. The enzyme electrode according to claim 1 or 2, wherein, with respect to said portion of the reaction layer which is superposed on said working electrode:

the total amount of proteins is 2.5 mg or less per cm² of said portion of said reaction layer;

the amount of DI in terms of the activity thereof is 0.25 U or more per cm² of said portion of said reaction layer;

the amount of 12α

-HSD in terms of the activity thereof is 0.63 U or more per cm² of said portion of said reaction layer; and

the amount of NADS in terms of the activity thereof is 0.063 U or more per cm² of said portion of said reaction layer.

4. The enzyme electrode according to any one of claims 1 to 3, wherein, with respect to said portion of the reaction layer which is superposed on said working electrode:

the total amount of proteins is 1.5 mg or less per cm² of said portion of said reaction layer;

the amount of DI in terms of the activity thereof is 1.0 U or more per cm² of said portion of said reaction layer;

the amount of 12α

-HSD in terms of the activity thereof is 2.5 U or more per cm² of said portion of said reaction layer; and

the amount of NADS in terms of the activity thereof is 0.25 U or more per cm² of said portion of said reaction layer.

5. The enzyme electrode according to any one of claims 1 to 4, wherein, with respect to said portion of the reaction layer which is superposed on said working electrode:

the total amount of proteins is 1.1 mg or less per cm² of said portion of said reaction layer;

the amount of DI in terms of the activity thereof is 2.5 U or more per cm² of said portion of said reaction layer;

the amount of 12α

-HSD in terms of the activity thereof is 6.25 U or more per cm² of said portion of said reaction layer; and

the amount of NADS in terms of the activity thereof is 0.625 U or more per cm² of said portion of said reaction layer.

6. A method for determining the concentration of adenosine triphosphate (ATP) in a sample, which comprises:

mixing a sample with an aqueous solution containing nicotinic acid adenine dinucleotide, a bile salt, an electron carrier and at least one member selected from the group consisting of ammonia and ammonium ion, to thereby obtain a sample solution;

contacting said sample solution with said working electrode, counter electrode and optionally reference electrode of the enzyme electrode of any one of claims 1 to 5, to thereby form an electric circuit through said sample solution;

measuring the electric current at said working electrode while applying a voltage to said enzyme electrode between the working electrode thereof and the counter electrode thereof or between the working electrode thereof and the reference electrode thereof to thereby perform an oxidation reaction of said electron carrier on the surface of said working electrode, wherein when said enzyme electrode does not contain a reference electrode, said voltage is applied between said working electrode and said counter electrode and wherein when said enzyme electrode contains a reference electrode, said voltage is applied between said working electrode and said reference electrode; and

calculating the amount of ATP, based on the measured value of said electric current at said working electrode.

7. A system for determining the concentration of adenosine triphosphate (ATP) in a sample, wherein said concentration of ATP is determined using nicotinic acid adenine dinucleotide, a bile salt, an electron carrier and at least one member selected from the group consisting of ammonia and ammonium ion,

said system comprising:

the enzyme electrode of any one of claims 1 to 5;

means for applying a voltage to said enzyme electrode between the working electrode thereof and the counter electrode thereof or between the working electrode thereof and the reference electrode thereof, said voltage being sufficient to perform an oxidation reaction of said electron carrier on the surface of said working electrode; and

means for measuring the electric current at said working electrode.

8. The system according to claim 7, which further comprises means for calculating the amount of ATP, based on the measured value of said electric current at said working electrode.