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

Pending Publication Date: 2022-04-15
南京合谷生命生物科技有限公司
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  • Application Information

AI Technical Summary

Problems solved by technology

[0003] 3,4-Dihydroxyphenylethanol, the traditional preparation method is to extract from olive oil or olive leaves, a large amount of flammable and explosive organic reagents such as ethyl acetate, absolute ethanol, dichloromethane, etc. are needed in the extraction process, and the extraction The yield is only 8.4%, the yield is low, and more by-products will be contained in the extraction process, resulting in lower purity of p-hydroxyphenethyl alcohol; the commonly used preparation method is generally prepared by synthesis, for example, Xiaoyan , Zhang Yang, etc. disclosed the synthesis method of hydroxytyrosol, reported that catechol and glyoxylic acid were used as raw materials to synthesize 3,4-dihydroxyphenylethanol through 3,4-dihydroxymandelic acid, and synthesized by four-step reaction 3,4-Dihydroxyphenylethanol was discovered, the total yield was 52.7%, and the yield was relatively low; there are other preparation methods using biological preparation methods, for example, a kind of engineering bacteria and its application disclosed in Chinese patent CN201710659225.1, reported co-express E. coli with L-amino acid oxidase, α-ketoacid decarboxylase, alcohol dehydrogenase, and NAD(P) reductase four enzymes to biosynthesize 2-phenylethanol, tyrosol, and hydroxytyrosol. Among them, The yield of 3,4-dihydroxyphenylethanol is 435mg / L, and the yield is relatively low; Chinese patent CN201710659225.1 discloses Escherichia coli expressing hydroxytyrosol and hydroxytyrosol glucoside and its construction method and application, and reports that the constructed Escherichia coli contains And be able to express ARO10, HpaBC and UGT genes, recombinant Escherichia coli tyrosine is expressed through related genes to obtain 3,4-dihydroxyphenylethanol, its yield can reach 401mg / L, and the yield is relatively low

Method used

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  • Method for preparing 3, 4-dihydroxyphenethyl alcohol through biological enzyme catalysis
  • Method for preparing 3, 4-dihydroxyphenethyl alcohol through biological enzyme catalysis
  • Method for preparing 3, 4-dihydroxyphenethyl alcohol through biological enzyme catalysis

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Experimental program
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Effect test

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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Abstract

The invention discloses a method for preparing 3, 4-dihydroxyphenethyl alcohol through bio-enzyme catalysis, which comprises the following steps: by taking escherichia coli fermentation liquor for inducing enzyme production as a raw material, centrifuging to obtain thalli, adding a buffer solution to suspend the thalli, introducing oxygen and the like, and adding a substrate p-hydroxyphenethyl alcohol and bio-enzyme catalysis to react to obtain the 3, 4-dihydroxyphenethyl alcohol. According to the method, the 3, 4-dihydroxyphenethyl alcohol is obtained through biological enzyme catalysis and biological synthesis by taking the p-hydroxyphenethyl alcohol as a substrate, the reaction condition is mild, no by-product is generated, and the residual quantity of the substrate is small; the catalytic efficiency of the biological enzyme is high and reaches 99%, and the yield of the product 3, 4-dihydroxyphenethyl alcohol reaches 13 g / L or above; the preparation method is green, environment-friendly and short in reaction period, can be applied to large-scale industrial production, and meets market requirements.

Description

technical field [0001] The invention relates to a method for preparing 3,4-dihydroxyphenethyl alcohol catalyzed by biological enzymes, belonging to the technical field of bioengineering. Background technique [0002] 3,4-Dihydroxyphenylethanol, also known as hydroxytyrosol, molecular formula C 8 h 10 o 3 , is a natural polyphenolic compound, found in olive oil and wastewater from olive oil processing, mainly esterified oleuropein can be hydrolyzed to obtain free 3,4-dihydroxyphenylethanol, studies have shown that 3 , 4-Dihydroxyphenylethanol has strong antioxidant activity. In addition, it also has a variety of biological and pharmacological activities, which can prevent osteoporosis, help diabetes, obesity and other diseases related to mitochondrial dysfunction. It can reduce the incidence of such diseases and is widely used in food industry, nutritional health care and cosmetics. Therefore, the extraction and preparation of 3,4-dihydroxyphenylethanol has certain practi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12P7/22
Inventor 王浩丁叶华夏
Owner 南京合谷生命生物科技有限公司
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