Method for preparing optical pure (R)-2-octanol by immobilized microorganism

A technology of immobilized microorganisms and immobilized cells, which is applied in the field of preparing optically pure (R)-2-octanol from immobilized microorganisms, can solve the problems of product separation being too complicated and cells not being reusable, and achieve the goal of reducing toxicity and durability The effect of strong acceptance and easy separation of products

Inactive Publication Date: 2009-08-12
XIANGTAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since microbial cells contain a complete enzyme system, for example, yeast cells contain rich oxidoreductase systems, which can realize the reduction and regeneration of coenzymes without adding expensive coenzyme factors, and there are few by-products, the yield is greatly improved, and the subsequent process is simplified. treatment process, but the cells cannot be reused, and the separation of products is still too complicated [Li Yongning et al., Pharmaceutical Biotechnology. 2006, 13(6): 446-450; Hu Jian et al., Acta Chemical Industry. 2006, 57(10): 2383-2387]

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0014] Wash the D-101 non-polar macroporous adsorption resin with deionized water for several times, soak it in 0.5% NaOH for 48 hours, wash it with deionized water until it is neutral, and dry it;

[0015] Insert baker's yeast into the culture medium for routine culture. The composition of the medium is that the components contained in each L of culture solution are in g: glucose 20.0, yeast extract 1.0, peptone 5.0, K 2 HPO 4 1.0, KH 2 PO 4 1.0, MgSO 4 0.2, prepare the bacterial liquid, soak the D-101 non-polar macroporous adsorption resin in the bacterial liquid, the temperature of the bacterial liquid is 30°C, the pH value is 6.5, the rotation speed of the shaking flask is 150rpm, the bacteria are fixed for 28 hours, and the bacteria are filtered out. solution, washed with saline, and heat-treated the immobilized cells for 15 min to prepare baker's yeast cells immobilized by non-polar macroporous adsorption resin.

[0016] Dissolve baker's yeast cells immobilized by D-...

Embodiment 2

[0018] Wash the H103 type non-polar macroporous adsorption resin with deionized water several times, soak it in 2.0% NaOH for 30 hours, wash it with deionized water until it is neutral, and dry it;

[0019] Insert baker's yeast into the culture medium for routine culture. The composition of the medium is that the components contained in each L of culture solution are in g: glucose 60.0, yeast extract 8.0, peptone 1.0, K 2 HPO 4 2.0, KH 2 PO 4 2.0, MgSO 4 0.5, to prepare the bacterial liquid, soak the H103 non-polar macroporous adsorption resin in the bacterial liquid, the temperature of the bacterial liquid is 28°C, the pH value is 7.0, the rotation speed of the shaking flask is 200rpm, the bacterial strain is fixed for 40h, the bacterial liquid is filtered off, and used After washing with physiological saline, the immobilized cells were heat-treated for 60 minutes to prepare baker's yeast cells immobilized by non-polar macroporous adsorption resin.

[0020] Dissolve baker...

Embodiment 3

[0022] Wash the HPD-300 non-polar macroporous adsorption resin with deionized water for several times, soak it in 4.0% NaOH for 24 hours, wash it with deionized water until it is neutral, and dry it;

[0023] Insert baker's yeast into the culture medium for routine culture. The composition of the medium is that the components contained in each L of culture solution are in g: glucose 30.0, yeast extract 4.0, peptone 6.0, K 2 HPO 4 1.0, KH 2 PO 4 2.0, MgSO 4 0.5, to prepare the bacterial liquid, soak the HPD-300 non-polar macroporous adsorption resin in the bacterial liquid, the temperature of the bacterial liquid is 28°C, the pH value is 7.0, the rotation speed of the shaking flask is 180rpm, the bacteria are fixed for 48 hours, and the bacteria are filtered out. solution, washed with saline, and heat-treated the immobilized cells for 55 minutes to prepare baker's yeast cells immobilized by non-polar macroporous adsorption resin.

[0024]Dissolve baker's yeast cells immobil...

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PUM

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Abstract

The invention discloses a method for preparing high optical pure (R)-2-octanol by a microbiological method, and a microorganism thereof. An immobilized-cell synthesis method of the invention has the advantages that: 1, an immobilization process is simple, and immobilized yeast cells have certain poison resistance, have excellent catalytic effect and can be repeatedly used in a reaction system; 2, the immobilized cells prepared by taking non-polar macroporous absorbent resin as a carrier are good in elasticity, strong in tolerance to temperature and pH, high in mechanical strength, stable in enzyme activity and long in half-life period; 3, as reaction is carried out in two phases of organic solvent/buffer solution, the toxic action of the organic solvent on the cells can be reduced, and the catalytic activity of the organic solvent is improved; and 4, the preparation of the optical pure (R)-2-octanol through the immobilized yeast cells is simple in process, free from need for no expensive coenzyme, mild in condition, short in reaction time, nearly free from byproducts, up to 90.25 percent e.e. in optical purity, simple in subsequent treatment, easy in product separation and friendly to environment.

Description

technical field [0001] A method for preparing optically pure (R)-2-octanol by microorganisms belongs to the technical field of microorganisms asymmetrically catalyzing prochiral compounds to synthesize optically pure compounds. Background technique [0002] 2-octanol, also known as 2-octanol, is often used in fine organic synthesis and can be used to produce chiral chemical materials and fragrances. (R)-2-octanol is an important chiral material for the preparation of high-performance liquid crystals and liquid crystal devices. It can greatly improve the quality of liquid crystals and change low-grade liquid crystals (achiral) into high-grade liquid crystals (chiral). At the same time, it is also an important intermediate for the synthesis of many optically active drugs and pesticides. Currently known methods for preparing optically pure 2-octanol mainly include three approaches: (1) chemical methods. Usually, optically pure 2-octanol is prepared by chemical method, which r...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12P7/04C12N11/02C12R1/865
CPCY02P20/50
Inventor 曾虹燕夏葵姜和蔡联辉黄理赵方方余静芳
Owner XIANGTAN UNIV
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