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Enzyme method for detaching and preparing L-methionine-15N and D-methionine-15N

A technology of enzymatic resolution and methionine, applied in the field of resolution of racemic compounds, can solve the problems of intermittent operation and small production scale, achieve the effects of no decrease in abundance, solution of decomposition in case of oxygen, and high optical purity

Inactive Publication Date: 2006-12-27
SHANGHAI RES INST OF CHEM IND
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since the 1950s, my country began to study chemical synthesis of methionine, and achieved success. Compared with foreign countries, the main gap is: small production scale, mainly intermittent operation

Method used

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  • Enzyme method for detaching and preparing L-methionine-15N and D-methionine-15N
  • Enzyme method for detaching and preparing L-methionine-15N and D-methionine-15N

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Experimental program
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Effect test

Embodiment 1

[0023] Take a storage slant, pick 5 rings of slant spores with an inoculation loop, put it into a triangular flask filled with 100ml sterile water, shake it well, and further dilute it to 10 -4 ~10 -8 times. Draw 0.2ml each into a 9cm-diameter plate filled with Zapei's medium, put it into a 30°C incubator and cultivate it for 3 days. After growing green spores, select a single colony and transfer it to the slant of Chapei's medium, and culture it in a 30°C incubator for 4 days. After growing green spores, add 3ml of sterile water to each tube, stir gently with a glass rod, and draw 0.5ml of the spore suspension was inserted into a 500ml Erlenmeyer flask filled with 50ml of soybean juice medium, and cultured at 30°C with shaking at 200rpm for 50h. After lowering the shaker, filter with suction, wash with distilled water, and collect aspergillus oryzae thallus pellets with a diameter of 2.0 to 3.0 mm for future use.

Embodiment 2

[0025] Weigh 5g of acetyl-DL-methionine solid, dissolve it with dilute NaoH, then adjust the volume to 500ml, then adjust the pH to about 7.0 with dilute hydrochloric acid, weigh 25g of wet free Aspergillus oryzae cells or 0.5g of aminoacyl Mix the enzyme powder into the prepared substrate, put the Erlenmeyer flask containing the substrate and enzyme in a water shaker at 37°C, 120 rpm and keep it warm for 48 hours to stop the reaction. At this time, the hydrolysis rate is close to 100%. . Evaporate the reaction solution to 1 / 5 of the original volume with a rotary evaporator at 45°C, adjust the pH to about 2 with 2mol / L hydrochloric acid, and flow through a 1500H strong Ion exchange columns for acidic cation exchange resins. Begin to collect effluent N-acetyl-DL-methionine- 15 N, wash the upper column with distilled water for 3 times, and then wash the column with distilled water until the effluent is colorless, pH neutral, and free of N-acetyl-DL-methionine- 15 When N flows...

Embodiment 3

[0027] Combine the water elution liquid on the column for the first time in Example 2, and concentrate it at 45°C to obtain N-acetyl-D-methionine- 15 N concentrated solution, which was hydrolyzed with 4mol / L hydrochloric acid at 90°C under nitrogen protection, N-acetyl-D-methionine- 15 The mass volume ratio of N to hydrochloric acid is 1:10, and the reflux reaction time is 5 hours. After the hydrolysis reaction is completed, under the protection of nitrogen, after the temperature drops to room temperature, adjust the pH to about 2 with 10mol / L NaoH, and flow through 300ml of 1500H type strongly acidic cation exchange with a flow rate of 0.04ml / min.g carrier at a constant speed. Resin ion exchange column, washed with water to remove impurities such as sodium chloride, until the effluent is colorless and Cl-free - Then use 0.2mol / L ammonia water to elute, collect single spots, concentrate at 45°C, catch ammonia, decolorize with activated carbon, and finally crystallize with eth...

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Abstract

This invention is associated with the method of preparation of L- Methionine -15N and D- Methionine -15N with enzymatic resolution. This method uses dissociate aspergillus oryzae mycelium cell or directly split DL- Methionine -15N with aminoacylase. It uses racemic acetyl- Methionine -15N (N-AC-DL-Met-15N) as raw material, and uses aminoacylase (EC.3,5,14) in dissociate aspergillus oryzae mycelium cell or aminoacylase powder as hydrolysis catalyst. The L- Methionine -15N and D- Methionine -15N obtained by this method have high output. It also has high chemical purity and optical purity.

Description

technical field [0001] The present invention relates to a method for resolving racemic compounds, a method for preparing biochemical products, and in particular to an enzymatic method for resolving and preparing L-methionine- 15 N and D-methionine- 15 N's method. Background technique [0002] Methionine is one of the basic units of protein and the only amino acid containing sulfur among the essential amino acids. In addition to participating in the transfer of methyl groups in animals, the metabolism of phosphorus and the synthesis of adrenaline, choline and creatine, it is also a protein and Raw material of cystine. Methionine cannot be synthesized in animals and needs to be ingested from food. Adding it to feed can promote the growth of poultry and livestock, increase the amount of lean meat and achieve the effect of shortening the feeding cycle. Adding 1kg of methionine to animal feed is equivalent to the nutritional value of 50kg of fishmeal, and the general adding am...

Claims

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Application Information

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IPC IPC(8): C12P13/12C12P41/00C12R1/69
Inventor 吕志贤罗凤山孙建春杜晓宁李良君
Owner SHANGHAI RES INST OF CHEM IND
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