JP2003210167A - Enzyme immobilization method and immobilized enzyme membrane - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To solve the problem of a conventional immobilized enzyme membrane having a high degree of technical difficulty wherein the immobilization of a target enzyme and the integration of the membrane usually having three phases are complicated and difficult. <P>SOLUTION: This enzyme immobilization method comprises introducing a silane coupling agent into a polymer membrane which is a phase on a specimen side, and then binding the target enzyme to the functional group of the introduced silane coupling agent through a divalent reagent, or the like. The immobilized enzyme membrane is prepared by sprinkling a different or identical polymer dissolved in a solvent on the enzyme-immobilized phase side to form and integrate the thin membrane. <P>COPYRIGHT: (C)2003,JPO

Description

Detailed Description of the Invention

[0001]

TECHNICAL FIELD The present invention relates to an enzyme immobilization method and an immobilized enzyme membrane which can be widely used in clinical, food, biochemical research fields and the like.

[0002]

2. Description of the Related Art Conventional immobilized enzyme membranes have been constructed by superposing the following three phases.

(A) Sample-side phase A polycarbonate membrane phase having pores with a pore diameter of about 50 nm. This pore size is a size that allows the target molecule to pass through but does not allow compounds having a higher molecular weight to pass through. For example, blood / serum samples do not pass through the components such as proteins.

(B) Enzyme-immobilized phase An enzyme-immobilized phase that causes an enzyme reaction with a target molecule. Usually, a functional group is bound to a certain kind of polymer compound, and the target enzyme is bound to the functional group by using a divalent reagent or the like.

(C) Probe (oxygen electrode, hydrogen peroxide electrode, ammonia electrode, etc.) side phase A thin film phase with pores having a pore diameter of about 0.5 nm. This pore size allows molecules after the enzymatic reaction, such as oxygen, hydrogen peroxide, and ammonia, to pass through,
It is a size that does not pass through the molecule before the enzymatic reaction.

In the above-mentioned three phases, in particular, the preparation of the enzyme-immobilized phase (b) is complicated and difficult.
It was also technically difficult to bond the two films) into one.

[0007]

As described above, the conventional immobilized enzyme membrane is technically difficult because it is complicated and difficult to immobilize the target enzyme and to form a single membrane.

[0008]

SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and has linearity and selection despite the fact that it is easy to immobilize an enzyme and prepare one phase for each phase. It is an object of the present invention to provide an immobilized enzyme membrane having excellent properties and mechanical strength, and an enzyme immobilization method for producing the same.

[0009]

The object of the present invention is to introduce a silane coupling agent into the polymer compound film, which is the phase on the sample side, and to introduce a divalent reagent into the functional group of the introduced silane coupling agent. An enzyme immobilization method in which an enzyme is bound through the enzyme immobilization method, and a thin film is formed on the enzyme immobilization phase side by sprinkling another kind or a high molecular compound of the same kind dissolved in a solvent, and the immobilized enzyme is made into one sheet. Achieved by the membrane.

Note When the polymer compound on the sample side is polycarbonate

In general, when a compound containing an amino group is introduced into a polycarbonate, an epoxy-like reaction occurs, and the compound collapses due to the resulting crosslinking via the amino group. However, in the present invention, such mechanical deterioration does not occur because the amino group is introduced into the surface phase of the film. When a silane coupling agent other than an aminated silane, for example, a thiolated silane is used, such a reaction naturally does not occur.

That is, according to the present invention, since the enzyme-immobilized phase and the sample-side phase are integrated at the initial stage of the preparation, the subsequent treatment is easy, and the target molecule and probe before the enzyme reaction are affected. The thin film treatment on the probe side, which is performed so that the given molecules (for example, hydrogen peroxide) cannot reach the probe, can be easily performed by using the polymer compound dissolved in the solvent. Also, since the treatment itself at each stage is simple, even a general person who does not have special equipment can obtain a stable immobilized enzyme membrane on the next day of the work, as long as the materials are prepared. In addition, since the materials used are generally available, the versatility and applicability are very wide.

[0013]

Detailed Description of the Structure of the Invention As the polymer compound used for the sample side film, a film having high mechanical strength such as polycarbonate is used. When polycarbonate is used, the compound may be produced by itself, but it is easiest to use a commercially available product having a pore size of 0.05 μm.

As the silane coupling agent required for immobilization, an aminated silane or a thiolated silane that can bind to divalent reagents is used.

The divalent reagent may be glutaraldehyde (for amino group) or N '-[2- (N
-Maleimido) ethyl] -N-piperazyl D-biotinamide hydrochloride (subject to thiol group) and the like are used.

As the enzyme to be immobilized, an enzyme suitable for the purpose is used. For example, glucose oxidase is used when a glucose responsive membrane is to be produced.

[0017]

DETAILED DESCRIPTION OF THE INVENTION

[0018]

[Examples] The raw materials and equipment used first will be described.

Polycarbonate membrane Millipore 0.0
5μm filter Model No. VMTP04700

Silane Coupling Agent Shin-Etsu Silicone N-β (aminoethyl) γ-aminopropylmethyldimethoxysilane Model No. KBM-602

Glucose oxidase Toyobo model number GLO-201

Glutaraldehyde manufactured by Wako Pure Chemical Industries 2
5% glutaraldehyde solution Model 079-00533

L-(+)-lysine manufactured by Tokyo Chemical Industry Co., Ltd. Model No. L019

Acetyl Cellulose Kodak Monoacetyl Cellulose Model No. 117-3251

Molecular Sieves Wako Pure Chemical Industries, Ltd. Molecular Sieves 3A 1/16 Model No. 134-060
95

Other reagents Special grades were used for ethyl alcohol and methyl acetate. The water used was ultrapure water supplied from an Millipore ultrapure water device.

In addition, glass plates, fluororesin seals, flat tweezers, beakers, petri dishes, variable pipettes, eyelet removers (9 mm, 15 mm), etc. were used as the equipment.

Manufacturing method

1. 800 mg of monoacetyl cellulose was dissolved in 80 mL of methyl acetate, and molecular sieves were added to remove water.

2. Add 8 mL of 1.6 mL of silane coupling agent.
It was dissolved in 0 mL of ethyl alcohol, and molecular sieves were added to remove water.

3. A fluororesin seal is attached to a glass plate, 100 μL of an ethanol solution of silane is dropped on the seal, and the polycarbonate film is gently placed on the solution with the non-glossy surface facing down, and the solution is applied to the entire lower surface. I put it off.

[Note] At that time, be careful that the solution does not wrap around to the surface side (upper surface).

4. After several minutes, it was confirmed that the solution was dry, and the same operation was repeated once again.

5. The end of the membrane was pinched with flat tweezers and washed several times with pure water in a beaker prepared in advance until the mottled pattern could not be seen.

6. The membrane was placed in a petri dish with the surface exposed to the solution facing up.

7. Glucose oxidase 25 mg 5
It was dissolved in mL of pure water, and after dissolution, 250 μL of 25% glutaraldehyde solution was added.

8. The glucose oxidase solution prepared above was poured into a petri dish containing a polycarbonate membrane and left overnight (12 hours) at room temperature.

9. After standing, the membrane was washed with water and placed in another petri dish.

10. L-(+)-lysine 50 mg to 5 m
It was dissolved in L of pure water and poured into the dish.

11.1 hours later, the membrane was washed with water, placed in another petri dish filled with pure water, and left for 2 hours.

12. After standing, the membrane was dried at room temperature.

The membrane was pierced with 13.15 mm eyelets, and the enzyme-immobilized surface (non-glossy surface) was placed on a glass plate with a fluororesin seal attached, and 50 μL of methyl acetate was placed in the center of the film. Then, the membrane was extended by dropping it from the above, and then 70 μL of an acetyl cellulose solution was added dropwise before the solution was dried and naturally dried at room temperature.

14. After drying, the immobilized enzyme membrane was pierced by removing 9 mm eyelets.

Note 15 mm and 9 mm eyelets are removed according to the hydrogen peroxide electrode probe to be used in future experiments. It is necessary to change the size to be hollowed out depending on the equipment used.

[0045]

[Experimental Example] The immobilized enzyme membrane of the example was attached to the measuring apparatus having the configuration shown in FIG. 1 to perform linearity and selectivity experiments.

Reagents used

Measurement buffer (phosphate buffer) EDTA
-2K 0.60 g, sodium benzoate 10.00
g, sodium chloride 3.00 g, disodium hydrogen phosphate monohydrate 7.49 g, sodium dihydrogen phosphate
1.91 g was dissolved in 1 L of pure water. pH 7.3.

Calibration solution for measurement (glucose concentration 180 mg
/ DL) α-d-glucose 1.80 g, sodium benzoate 2.00 g, EDTA-2K 1.00 g
Was dissolved in 1 L of pure water.

Calibration solution for sample (phosphate buffer solution) Solution A (0.2 M sodium hydrogen phosphate 360 mL, 0.2 M
A mixture of 140 mL of sodium dihydrogen phosphate),
50 mL of solution B (3.0 M sodium chloride),
And 10 g of sodium azide were added and diluted to 1 L with pure water.

Experimental method

Linearity

Using the immobilized enzyme membrane of Example, the α-d-glucose concentration was 0, 50, 100, and
A sample prepared to have a concentration of 150, 200, 300, 400, 500 mM was diluted 24 times with pure water, and its current value was measured at n = 2.

Selectivity

L-ascorbic acid was added to a mixture of 10% sodium azide and the above buffer at a ratio of 1:99 at a concentration of 10 mM (176.13 mg / dL), 100 m.
It was dissolved so as to have M (1761.3 mg / dL), and the two solutions were diluted 24 times with pure water and measured as a sample.

Result

The results of the linearity and selectivity experiments are shown in Table 1,
The results are shown in Table 2.

[0057]

[Table 1]

[0058]

[Table 2]

[0059]

INDUSTRIAL APPLICABILITY As described above, according to the present invention, a silane coupling agent is introduced into a polymer film, which is a phase on the side of a sample, and the functional group thereof is bound with an enzyme through a divalent reagent. Method, and on the side of the enzyme immobilization phase, a thin film is formed by sprinkling another type or a polymer compound of the same type dissolved in a solvent, and by adopting a single immobilized enzyme membrane, Immobilized enzyme membranes with excellent linearity, selectivity, and mechanical strength, which are easy to immobilize and prepare for each phase, are used in various research fields such as clinical, food, and biochemistry. Can be provided to. Also, since the treatment itself at each stage is simple, even a general person who does not have special equipment can obtain a stable immobilized enzyme membrane on the next day of the work, as long as the materials are prepared. In addition, since the materials used are generally available, the versatility and applicability are very wide.

[Brief description of drawings]

FIG. 1 is a diagram showing the configuration of a measuring device used when an immobilized enzyme membrane using the enzyme immobilization method of the present invention is used.

[Explanation of symbols]

1. Immobilized enzyme membrane 2 ... Probe (hydrogen peroxide electrode, etc.) 3 ... Measuring cell 4 ... Buffer solution or sample solution 5 ... External power supply 6 ... Ammeter or resistance 7: Recorder

Claims (5)

[Claims] 1. An enzyme immobilization method and an immobilized enzyme membrane, wherein a silane coupling agent is introduced into a membrane made of a high molecular compound, and a target enzyme is bound to a functional group of the silane coupling agent. 2. An enzyme immobilization method and an immobilized enzyme membrane, wherein the polymer compound is polycarbonate. 3. The enzyme immobilization method and the immobilized enzyme membrane according to claim 1, wherein the silane coupling agent is an aminated silane. 4. A thin film is formed by integrating a polymer compound dissolved in a solvent on the enzyme-immobilized phase side of the polymer compound film to form an integrated film,
3. Enzyme immobilization method and immobilized enzyme membrane according to 3. 5. The immobilized enzyme membrane according to claim 1, wherein the thin film is acetyl cellulose.