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A kind of production method of L-glufosinate-ammonium

A production method, glufosinate-ammonium technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve problems such as low process efficiency, and achieve the effects of low environmental protection pressure, high conversion rate of raw materials, and low cost

Active Publication Date: 2018-12-11
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

But this process efficiency is low, when the concentration of substrate PPO is 552mmol / L, under the situation of almost completely consuming about 700mmol / L raw material L-aspartic acid, only generate the product L-PPT of 251.9mmol / L, and At the same time, about 234.5mmol / L of impurity alanine was generated

Method used

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  • A kind of production method of L-glufosinate-ammonium
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  • A kind of production method of L-glufosinate-ammonium

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Experimental program
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Effect test

Embodiment 1

[0049] 1. Cloning transaminase genes from the genomes of Escherichia coli E.coli K12W3110, Bacillus subtilis 168 and Bacillus magaterium YYBM1 respectively, according to the corresponding genome DNA sequences (GenBank accession numbers are CP012868.1, CP010052.1 and CP001982 .1) Design corresponding PCR upstream primers and downstream primers.

[0050] Primers for transaminases derived from E.coli:

[0051] EC-F sequence: 5'-CCG GAATTC ATGAGCAACAATGAATTCCATC-3' (EcoRI)

[0052] EC-R sequence: 5'-CCG CTCGAG TTAATCGCTCAGCGCATCC-3'(XholI)

[0053] Primers for transaminases derived from Bacillus Subtilis:

[0054] BS-F sequence: 5'-CCC GAGCTC ATGAGTCAAAACAACAGCAAGCATCA-3'(SacI)

[0055] BS-R sequence: 5'-CCC AAGCTT TTAAGCTCGCAGGCCCGCCT-3' (HindIII)

[0056] Primers for transaminases from Bacillus magaterium:

[0057] BM-F sequence: 5'-CGC GGATCC ATGAGTCAAACTTTTAGCAA-3' (BamHI)

[0058] BM-R sequence: 5'-CCC AAGCTT TTACACTTCAACCGTTTGCT-3' (HindIII)

[0059] Restr...

Embodiment 2

[0074] 1. The cultivation of microorganisms

[0075] Composition of LB liquid medium: peptone 10g / L, yeast powder 5g / L, NaCl 10g / L, dissolved in deionized water and then constant volume, sterilized at 121°C for 20min, ready for use.

[0076] The genetically engineered bacteria E.coli BL21(DE3) containing the transaminase gene was inoculated into 5 mL LB liquid medium containing 50 μg / mL kanamycin, and cultured with shaking at 37°C for 12 hours. Transfer to 500mL fresh LB liquid medium also containing 50μg / ml Kan, and shake culture at 37°C until OD 600 When it reaches about 0.8, add IPTG to its concentration of 0.3mM, and induce culture at 28°C for 20h. After the cultivation, the culture solution was centrifuged at 10,000 rpm for 10 min, the supernatant was discarded, the bacteria were collected, and stored in a -70°C ultra-low temperature refrigerator until use.

[0077] 2. Preparation of crude enzyme solution

[0078]The bacterial cells collected after the cultivation were...

Embodiment 3

[0080] Quantitatively weigh PPO, alanine and pyridoxal phosphate, mix them in a beaker, adjust the pH of the solution to 7.5 with 30% ammonia water, add it to a volumetric flask, and dilute to volume with deionized water to obtain a final concentration of PPO of 60 mM and alanine The final concentration of acid is 180mM, and the final concentration of pyridoxal phosphate is 1mM.

[0081] Cultivate genetically engineered bacteria capable of expressing the transaminase shown in SEQ ID NO.1 (derived from Escherichia coli E.coli K12W3110), take 1mL of the culture solution, centrifuge at 10000rpm for 10min, discard the supernatant to obtain 5mg of cells; add to 1mL of the above-mentioned mixed solution, resuspended, and reacted in a metal bath shaking reactor at 37°C for 24 hours.

[0082] After the reaction was completed, HPLC detection was carried out, and L-glufosinate-ammonium was generated, but no obvious PPO peak was found, indicating that the conversion rate of PPO reached 1...

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Abstract

The invention discloses a production method of L-glufosinate. The method includes the steps that with 2-carbonyl-4-(hydroxyl methyl phosphoryl) butyric acid and salt thereof being a substrate, isolated transaminase or a cell catalysis substrate of in-vitro expression transaminase reacts with an amino donor under the condition that the amino donor exists, so that L-glufosinate is obtained, wherein the amino donor is alanine, and the amino acid sequence of transaminase is shown in SEQ ID NO.1-3. With 2-carbonyl-4-(hydroxyl methyl phosphoryl) butyric acid and salt thereof being the substrate and alanine being the amino donor, the transamination reaction occurs through the specific transaminase catalysis substrate, the substrate can be completely converted into L-glufosinate, and the conversion rate of raw materials is high and can reach 100%.

Description

technical field [0001] The invention relates to the field of biochemical technology, in particular to a method for producing L-glufosinate-ammonium; specifically, a method for producing optically pure L-glufosinate-ammonium by a biological enzymatic method. Background technique [0002] Glufosinate-ammonium, English name: Phosphinothricin (abbreviated as PPT), generally refers to the compound 2-amino-4-[hydroxy(methyl)phosphono]-butyric acid or its salt formed with a basic compound. Glufosinate-ammonium is a broad-spectrum contact herbicide developed by Hearst in the 1980s (later owned by Bayer). It belongs to the phosphonic acid herbicide and is an inhibitor of glutamine synthesis. It is transferred in the leaves, but cannot Transferred elsewhere, the inhibition of glutamine synthesis leads to the accumulation of ammonium ions and the disintegration of chloroplasts, thereby inhibiting photosynthesis and eventually leading to plant death. [0003] [0004] Glufosinate-am...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12P13/04C12N9/10C12R1/19
CPCC12N9/1096C12P13/04C12Y206/01002
Inventor 杨立荣周海胜蒙丽钧刘善和韦永飞谷顺明袁晓路方红新刘亚运徐刚吴坚平
Owner ZHEJIANG UNIV
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