Unlock instant, AI-driven research and patent intelligence for your innovation.

Method for producing (r)-4-substituent phenethyl alcohol by catalytic reduction of acetic acid bacteria

A technology of Acetobacter and acetophenone, applied in the field of asymmetric synthesis of biocatalytic chiral compounds, can solve the problems of inhibition, low catalyst activity, free microbial cell toxicity, etc., to increase stability and be beneficial to recycling. Effect

Inactive Publication Date: 2011-12-07
SOUTH CHINA UNIV OF TECH
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The main reason may be that the activity of the catalyst is not high, and it is inhibited by substrates and products.
But the yield is very low, the main reason may be that there is a reverse reaction in the aqueous phase to oxidize the product alcohol to ketone and serious product and substrate inhibition, and the free microbial cells are easily poisoned by the substrate, resulting in a decrease in cell activity

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for producing (r)-4-substituent phenethyl alcohol by catalytic reduction of acetic acid bacteria
  • Method for producing (r)-4-substituent phenethyl alcohol by catalytic reduction of acetic acid bacteria

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0060] Put 2g of Chinese kefir grains into a 250mL Erlenmeyer flask filled with 100mL of tomato medium, culture at 28°C for 24h, and transfer and culture continuously in tomato medium for 3 times under the same conditions. Bacterial solution was properly diluted and spread on solid separation medium by ten-fold dilution method, and cultured at 28°C for 24-36 hours to obtain a single colony. After purification, the slant was preserved for identification. Tomato medium: tomato juice 200mL / L, yeast extract 10g / L, glucose 10g / L, peptone 10g / L, pH 6.0.

[0061] The strain XZY003 identified as Acetobacter was transferred from the slant to the tomato medium, cultured at 30°C, 160r / min for 24h, centrifuged (3500r / min, 15min, 4°C), washed twice to obtain wet bacteria. Then disperse the wet cells in distilled water of equal weight, then add 4 times the weight concentration of the wet cells to 20g / L sodium alginate, stir evenly, and use 5 # Inject the above suspension into 200 mL of CaC...

Embodiment 2

[0063] The strain XZY003 identified as Acetobacter was transferred from the slant to the tomato medium, cultivated at 30°C, 160r / min for 24h, centrifuged (8000r / min, 10min, 4°C), washed twice, and wet cells were obtained. Then disperse the wet cells in distilled water of equal weight, and then add 6 times the weight concentration of the wet cells to 10g / L sodium alginate, stir evenly, and use 5 # Inject the above suspension into 200 mL of CaCl with a concentration of 20 g / L 2 solution, harden at 4°C for 4 hours, wash the hardened calcium alginate gel balls (diameter 2-3mm) with distilled water three times, and then transfer into 200mL containing CaCl 2 In the glucose solution, the final concentration is 0.5g / L CaCl 2 , 200g / L glucose, placed in 4 ℃ of refrigerators and preserved for later use, the immobilized Acetobacter cell granule of the wet thalline that obtains by embodiment 2, its diameter size is 2-3mm, spherical shape, general mechanical strength, its cell content 10...

Embodiment 3

[0065]The triethanolamine hydrochloride buffer solution (triethanolamine concentration in hydrochloric acid is 0.1mol / L, pH 7.0) of 4mL is packed in the Erlenmeyer flask of tool stopper, then add the immobilized Acetobacter cell of the wet thalline prepared in embodiment 2 respectively Particles and isopropanol and 4-bromoacetophenone form a mixture, and the concentrations of isopropanol and 4-bromoacetophenone in the mixture are 130.6mmol / L and 6mmol / L respectively, at 30°C, 180r / min, immobilized Acetobacter The weight-to-volume ratio of the cell particles to the mixture was 1.0 g / mL, and the reaction was carried out for 2 hours to obtain (R)-4-bromophenethyl alcohol. The yield of (R)-4-bromophenethyl alcohol was 85.4% by gas phase detection, and the enantiomeric purity of (R)-4-bromophenethyl alcohol was More than 99% e.e.

[0066] Gas phase detection method: The initial temperature of the chromatographic column is 145°C, and after maintaining for 10 minutes, it rises to 150...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
Login to View More

Abstract

The invention discloses a method for producing (R)-4-substituent phenethyl alcohol by catalytic reduction of acetic acid bacteria. In the hydrochloric acid buffer solution of triethanolamine, the substrate 4-substituent acetophenone, isopropanol and acetic acid of wet bacteria are added. The immobilized cell particles of bacillus form a mixture, adjust the pH value to 4.0-7.0, and shake the reaction for 2-12 hours at a temperature of 25-35°C and a rotation speed of 160-260r / min to obtain (R)-4- The substituent is phenylethyl alcohol; the weight-to-volume ratio of the immobilized Acetobacter sp. cell particles to the mixture is 0.1-1.0 g / ml; the preservation number of Acetobacter sp. XZY003 is CCTCCM209061. The enantiomer pure (R)-4-substituent phenylethanol product obtained by the invention has an enantiomer purity of more than 99% e.e., and the enantiomer purity and yield of the product are both improved.

Description

technical field [0001] The invention belongs to the technical field of biocatalytic asymmetric synthesis of chiral compounds, and in particular relates to the preparation of (R)-4-substituent phenethyl alcohol by catalyzing the asymmetric reduction of aromatic ketones through the application of acetic acid bacteria. Background technique [0002] Chiral aromatic alcohols are important intermediates in the synthesis of pharmaceuticals, agricultural chemicals, and natural products, and the asymmetric reduction of ketones is one of the most important and practical methods for the preparation of enantiomerically pure chiral alcohols. Enantiomerically pure 1-(4-methoxy)-phenylethanol is an important chiral intermediate, and (R)-1-(4-methoxy)-phenylethanol can be used to synthesize 3-aryl Base-3-substituted propionic acid anti-inflammatory drugs, and (S)-1-(4-methoxy)-phenylethanol is an important synthon for the synthesis of anti-allergic drugs. Since different stereoisomers of c...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12P7/22C12R1/02
Inventor 娄文勇宗敏华肖仔君
Owner SOUTH CHINA UNIV OF TECH