Method for preparing sucrose ester through whole-cell catalysis
A whole-cell catalyst and catalytic preparation technology, applied in biochemical equipment and methods, microorganism-based methods, microorganisms, etc., can solve the problems of difficult product separation and extraction, long growth cycle of fermentation method, low substrate conversion rate, etc., to achieve High operational stability, beneficial to the protection of the environment, and the effect of simplifying the product separation steps
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Embodiment 2
[0032] Add 5g / L yeast extract, 5g / L ammonium sulfate, 1g / L dipotassium hydrogen phosphate, 0.2g / L crystalline magnesium sulfate and 5g / L anhydrous glucose in 1L distilled water to induce culture Pseudomonas stutzeri, collected by centrifugation after 48 hours of culture, and freeze-dried whole-cell catalyst; 60 mg of sucrose, 0.06 g (the mass ratio of sucrose to whole-cell catalyst is 1:1) whole-cell catalyst of Pseudomonas stutzeri Cell catalyst, 20 mmoL (1:50 molar ratio of sucrose to acyl donor) vinyl methacrylate and 2 ml tert-amyl alcohol / dimethyl sulfoxide (5:1 volume ratio) dual-solvent medium Put it in a Erlenmeyer flask and vibrate in an air bath constant temperature oscillator at 40 °C and 200 rpm. After 48 h of reaction, the reaction conversion rate is 48.4%.
Embodiment 3
[0034] Add 5g / L yeast extract, 5g / L ammonium sulfate, 1g / L dipotassium hydrogen phosphate, 0.2g / L crystalline magnesium sulfate and 5g / L anhydrous glucose in 1L distilled water to induce culture Pseudomonas stutzeri, collected by centrifugation after 48 hours of culture, and freeze-dried whole-cell catalyst; mix 60 mg sucrose, 0.06 g (the mass ratio of sucrose to whole-cell catalyst is 1:1) Pseudomonas stutzeri Whole-cell catalyst, 20 mmoL (1:50 molar ratio of sucrose to acyl donor) vinyl methacrylate, and 2 ml tert-amyl alcohol / dimethylsulfoxide (5:1 volumetric ratio) dual-solvent medium Placed in a stoppered Erlenmeyer flask, placed in an air bath constant temperature oscillator at 50 °C and 200 rpm, and oscillated after 48 hours of reaction, the reaction conversion rate was 24.9%.
Embodiment 4
[0036] Add 10g / L yeast extract, 10g / L ammonium sulfate, 2g / L dipotassium hydrogen phosphate, 0.4g / L crystalline magnesium sulfate and 10g / L anhydrous glucose in 1L distilled water to induce culture Pseudomonas stutzeri, collected by centrifugation after 48 hours of culture, and freeze-dried whole-cell catalyst; 60 mg of sucrose, 0.06 g (the mass ratio of sucrose to whole-cell catalyst is 1:1) whole-cell catalyst of Pseudomonas stutzeri Cell catalyst, 20 mmoL (1:50 molar ratio of sucrose to acyl donor) vinyl methacrylate and 2 ml tert-amyl alcohol / dimethyl sulfoxide (5:1 volume ratio) dual-solvent medium Put it in a Erlenmeyer flask and vibrate in an air bath constant temperature oscillator at 40 °C and 200 rpm. After 48 h of reaction, the reaction conversion rate was 14.2%.
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