Oxidoreductase for improving electrochemical activity and biosensor containing oxidoreductase
A biosensor and reductase technology, applied in the field of electrochemistry, can solve problems such as difficult and precise control of preparation, uncertainty of performance of glucose monitoring system, etc., and achieve the effect of improving catalytic oxidation efficiency
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Embodiment 1
[0061] First, 2 mg / mL glucose oxidase was incubated in PBS buffer solution containing 3 mol / L urea (preferred value: 3) at 4° C. for 12 hours to fully develop the glucose oxidase. Then mix 2mg / mL of ruthenium or osmium complex with free amino group with 2mg / mL of glucose oxidase, then add 2mmol / L of carbodiimide and 0.5mmol / L of N-hydroxysuccinyl Imine, after mixing well, reacted at 4°C for 12h. Then, the modified perglucose oxidase was separated and purified by ultrafiltration bag dialysis (cut molecular weight: 10000).
Embodiment 2
[0063] First, incubate 1 mg / mL glucose oxidase in PBS buffer solution containing 8 mol / L urea at 4°C for 24 hours to fully develop the glucose oxidase. Then mix 1 mg / mL of ruthenium or osmium complex with free amino group with 10 mg / mL of glucose oxidase, and then add 1 mmol / L of carbodiimide and 1 mmol / L of N-hydroxysuccinyl Imine, after mixing well, reacted at 4°C for 24h. Then, the modified perglucose oxidase was separated and purified by ultrafiltration bag dialysis (cutting molecular weight: 30000).
Embodiment 3
[0065] First, incubate 10 mg / mL glucose oxidase in PBS buffer solution containing 1 mol / L urea at 4°C for 18 hours to fully develop the glucose oxidase. Then mix 10 mg / mL of ruthenium or osmium complex with free amino groups with 1 mg / mL of glucose oxidase, and then add 10 mmol / L carbodiimide and 0.1 mmol / L N-hydroxysuccinate in sequence Imide, after mixing well, reacted at 4°C for 18h. Then, the modified perglucose oxidase was separated and purified by ultrafiltration bag dialysis (cut molecular weight: 1000).
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