Method for preparing 3, 4-dihydroxyphenethyl alcohol through biological enzyme catalysis
A technology of dihydroxyphenylethanol and p-hydroxyphenylethanol, which is applied in the field of biological enzyme catalysis to prepare 3,4-dihydroxyphenylethanol, can solve the problems of low purity, low yield, and low output of hydroxyphenylethanol, and meet the needs of the market required, high catalytic efficiency, and low substrate residue
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Embodiment 1
[0031] (1) Place the Escherichia coli MG1655 fermentation broth induced to produce enzymes in a centrifuge tube, centrifuge for 3 minutes in a centrifuge with a rotating speed of 2000rpm / min, remove the centrifuge supernatant, and collect the bacteria;
[0032] (2) Add 90ml PB buffer solution to the thalline to suspend the thalline, and the biomass of the thalline is 15g / m 3 , and then pour it into a four-necked flask, then put the four-necked flask into a magnetic stirring water bath with a rotating speed of 200rpm / min and a temperature of 25°C, and then feed oxygen into the bacterial suspension at an oxygen flow rate of 0.5L / min. And use ammonia water to adjust the pH value to 5.5 in real time;
[0033] (3) Weigh 0.5g of p-hydroxyphenylethanol substrate, dissolve it in 10ml of PB buffer, after it is completely dissolved, add 0.5g / 30min dropwise into the four-neck flask once, and keep stirring for reaction, and then pass the liquid phase detection The p-hydroxyphenylethanol ...
Embodiment 2
[0035] (1) Place the Escherichia coli MG1655 fermentation broth induced to produce enzymes in a centrifuge tube, centrifuge for 3 minutes in a centrifuge with a rotating speed of 2000rpm / min, remove the centrifuge supernatant, and collect the bacteria;
[0036] (2) Add 40ml PB buffer solution to the thalline to suspend the thalline, and the biomass of the thalline is 42g / m 3 , and then pour it into a four-necked flask, then put the four-necked flask into a magnetic stirring water bath with a rotating speed of 200rpm / min and a temperature of 25°C, and then feed oxygen into the bacterial suspension at an oxygen flow rate of 0.5L / min. And use ammonia water to adjust the pH value to 5.5 in real time;
[0037](3) Weigh 0.5g of p-hydroxyphenylethanol substrate, dissolve it in 1.5ml PB buffer solution, completely dissolve and mix well, then add dropwise at 0.5g / 30min in a four-neck flask, and keep stirring for reaction, then Detect the p-hydroxyphenylethanol substrate in the reactio...
Embodiment 3
[0039] (1) Place the Escherichia coli MG1655 fermentation broth induced to produce enzymes in a centrifuge tube, centrifuge for 3 minutes in a centrifuge with a rotating speed of 2000rpm / min, remove the centrifuge supernatant, and collect the bacteria;
[0040] (2) Add 250ml PB buffer solution to the thalline to suspend the thalline, and the biomass of the thalline is 15g / m 3 , and then pour it into a four-necked flask, then put the four-necked flask into a magnetic stirring water bath with a rotating speed of 200rpm / min and a temperature of 25°C, and then feed oxygen into the bacterial suspension at an oxygen flow rate of 0.5L / min. And use ammonia water to adjust the pH value to 5.5 in real time;
[0041] (3) Weigh 3.25g of p-hydroxyphenylethanol substrate, dissolve in 20ml of PB buffer, completely dissolve and mix well, then add dropwise to the four-necked flask five times at 0.65g / 30min, and keep stirring for reaction, then Detect the p-hydroxyphenylethanol substrate in th...
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