Activity detection method of ester type catechin synthetase
A technology for detection of ester-type catechin and activity, which is applied in the direction of biochemical equipment and methods, measurement/inspection of microorganisms, etc., can solve the problems that there is no detection method for the activity of ester-type catechin synthase, and achieve the improvement of tea High quality, simple operation and short detection time
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Embodiment 1
[0050] Main equipment: 1. High performance liquid chromatography (HPLC); 2. Constant temperature water bath; 3. Rotary evaporator; 4. Centrifuge; 5. pH meter;
[0051] Materials and Reagents:
[0052]1. Materials to be tested: fresh leaves of tea trees (stored at -80°C for later use);
[0053] 2. Main reagents
[0054] (1) Polyvinylpyrrolidone (PVPP), purchased from Shanghai Suolaibao Biotechnology Co., Ltd., is used to adsorb polyphenols in the enzyme solution and maintain a high activity of the enzyme protein;
[0055] (2) Quartz sand (commercially available): increase friction and improve the extraction rate of enzyme protein;
[0056] (3) 0.1 mol / L pH7.4 phosphate buffer
[0057] Solution A: Weigh sodium dihydrogen phosphate (NaH 2 PO 4· 2H 2 (0) 7.8 grams, dissolved in 500mL of distilled water;
[0058] Solution B: Weigh disodium hydrogen phosphate (Na 2 HPO 4· 3H 2 (2) 17.9 grams, be dissolved in the distilled water of 500mL, standby;
[0059] Before use, take...
Embodiment 2
[0104] Main equipment is the same as embodiment 1.
[0105] Materials and Reagents:
[0106] 1. Detected material: same as embodiment 1;
[0107] 2. Main reagents:
[0108] Reaction substrate: 3.8 mmol / L epigallocatechin (EC) solution: weigh 0.0011 g of EC and dissolve it in 1 mL of water, and store it below 4°C for future use. Other reagents are with embodiment 1;
[0109] A method for detecting the activity of ester catechin synthase comprises the following steps:
[0110] 1.1. Preparation of enzyme solution
[0111] With embodiment 1;
[0112] 1.2. Determination of enzyme activity
[0113]1.2.1. Preparation of reaction solution
[0114] Mix 0.46mL enzyme solution, 0.3mL antioxidant, 0.074mL hydrolysis inhibitor, 0.15mL reaction substrate epigallocatechin (EC) solution, 0.075mL reaction substrate 1-O-galloyl-β-D-glucose (βG) solution and 0.59mL phosphate buffer were mixed evenly, and reacted in a water bath at a temperature of 30°C for 60 minutes to obtain a reaction...
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