Novel use of acetate-containing small molecules as peroxidases acting as catalysts
A technology of peroxidase and small molecules, applied in the field of simulated enzymes, can solve the problems of limited sources, extensive development and use restrictions, heat sensitivity and poor stability of horseradish peroxidase, and achieve easy access and low price Inexpensive, good stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] The mensuration of embodiment 1 peroxidase activity
[0033] Dissolve 0.82g of sodium acetate in 10mL of water, and add 0.1mL of the above solution into 0.9mL of buffer systems with different pHs (including 0.05mol / L Tris-HCl, 1mmol / L H 2 o 2 , 1mmol / L 2,2-azino-bis(3-ethyl-benzothiazole-6-sulfonic acid) diammonium salt (ABTS)).
[0034] The result is as figure 1 As shown, the small molecule has a good catalytic effect under the conditions of pH 1.0, 2.0, 3.0, 4.0, 5.0, and 6.0. The darker the color, the better the catalytic effect.
Embodiment 2
[0035] Preparation and application of embodiment 2 hydrogen peroxide detection test paper
[0036] (1) Preparation of impregnation solution: Take a 1000mL beaker, add 40mL sodium alginate solution (concentration is 50g / L), add 10mL 1% (v / v) Tween 80 solution, add 40mL gelatin solution (concentration is 80g / L) L), add 100mL pH 5.0 acetic acid-sodium acetate buffer solution (100mM sodium acetate), 10mL potassium iodide (50g / L), 10g polyvinylpyrrolidone, 0.5g brilliant blue, and mix well to obtain an impregnation solution;
[0037] (2) Immersion paper: Pour the impregnation solution prepared in step (1) into a glass dish, soak the filter paper, scrape off the excess solution with a glass rod, and dry it in a blast oven at 40°C for 30 minutes. After drying, it is Light blue test paper, obtains described hydrogen peroxide detection test paper.
[0038] like figure 2 As shown, the different concentrations of hydrogen peroxide to be tested (0 μM, 10 μM, 20 μM, 50 μM, 100 μM, 1000 ...
Embodiment 3
[0039] Preparation and application of embodiment 3 hydrogen peroxide detection test paper
[0040] (1) Preparation of impregnation solution: Take a 1000mL beaker, add 40mL sodium alginate solution (concentration is 50g / L), add 10mL 1% (v / v) Tween 80 solution, add 40mL gelatin solution (concentration is 80g / L) L), add 100mL pH 5.0 acetic acid-potassium acetate buffer solution (100mM potassium acetate), 10mL potassium iodide (50g / L), 10g polyvinylpyrrolidone, 0.5g brilliant blue, and mix well to obtain an impregnation solution;
[0041] (2) Immersion paper: Pour the impregnation solution prepared in step (1) into a glass dish, soak the filter paper, scrape off the excess solution with a glass rod, and dry it in a blast oven at 40°C for 30 minutes. After drying, it is Light blue test paper, obtains described hydrogen peroxide detection test paper.
[0042] Different concentrations of hydrogen peroxide (0 μM, 10 μM, 20 μM, 50 μM, 100 μM, 1000 μM, 2000 μM) to be tested were droppe...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com