Methods for making L-glufosinate
US-11913048-B2 · Feb 27, 2024 · US
US12305207B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12305207-B2 |
| Application number | US-202418435544-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 7, 2024 |
| Priority date | Mar 2, 2016 |
| Publication date | May 20, 2025 |
| Grant date | May 20, 2025 |
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Methods for the production of L-glufosinate (also known as phosphinothricin or (S)-2-amino-4-(hydroxy(methyl)phosphonoyl)butanoic acid) are provided. The methods comprise a two-step process. The first step involves the oxidative deamination of D-glufosinate to PPO (2-oxo-4-(hydroxy(methyl)phosphinoyl)butyric acid). The second step involves the specific amination of PPO to L-glufosinate, using an amine group from one or more amine donors. By combining these two reactions, the proportion of L-glufosinate in a mixture of L-glufosinate and D-glufosinate can be substantially increased.
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What is claimed is: 1. A method for making L-glufosinate, comprising: reacting D-glufosinate with a D-amino acid oxidase (DAAO) enzyme to form 2-oxo-4-(hydroxy(methyl)phosphinoyl) butyric acid (PPO); and aminating the PPO to L-glufosinate using an L-amino acid dehydrogenase (LAAD) enzyme in the presence of an ammonia source and a redox cofactor acceptor. 2. The method according to claim 1 , further comprising the step of recycling the redox cofactor acceptor. 3. The method according to claim 1 , wherein the D-glufosinate is originally present in a racemic mixture of D- and L-glufosinate or salts thereof. 4. The method according to claim 1 , wherein the DAAO enzyme has the amino acid sequence of SEQ ID NO: 2. 5. The method of claim 1 , wherein the DAAO enzyme is a mutant DAAO comprising one or more mutations at positions 54, 56, 58, 213, and 238, using SEQ ID NO: 2 as a reference sequence. 6. The method of claim 5 , wherein the mutation at position 54 is selected from the group consisting of N54C, N54L, N54T, and N54V. 7. The method of claim 5 , wherein the mutation at position 56 is T56M. 8. The method of claim 5 , wherein the mutation at position 58 is selected from the group consisting of F58A, F58G, F58H, F58K, F58N, F58Q, F58R, F58S, and F58T. 9. The method of claim 5 , wherein the mutation at position 213 is M213S. 10. The method of claim 5 , wherein the mutant DAAO comprises mutations at positions 54 and 56, using SEQ ID NO: 2 as a reference sequence. 11. The method of claim 5 , wherein the mutant DAAO comprises mutations F58Q or F58H, using SEQ ID NO: 2 as a reference sequence. 12. The method of claim 5 , wherein the mutant DAAO comprises mutations N54V and F58Q, using SEQ ID NO: 2 as a reference sequence. 13. The method of claim 5 , wherein the mutant DAAO comprises mutations N54V, F58Q, and M213S, using SEQ ID NO: 2 as a reference sequence. 14. The method of claim 1 , wherein the reacting step and the aminating step are performed in a single container. 15. The method of claim 14 , wherein all reagents are substantially added at the start of the reaction. 16. The method of claim 14 , wherein the reagents for the reacting step and the reagents for the aminating step are added to the single container at different times. 17. The method of claim 1 , wherein the reacting step and the aminating step are performed in separate containers. 18. The method of claim 1 , wherein reacting D-glufosinate with the DAAO enzyme is conducted while aerating. 19. The method of claim 18 , wherein the aerating comprises introducing oxygen, oxygen enriched air, an oxygen enriched gas stream, or air. 20. The method of claim 18 , wherein the aerating is conducted intermittently or continuously.
acting on the CH-NH2 group of donors (1.4) · CPC title
D-Amino acid oxidase (1.4.3.3) · CPC title
D-Amino-acid oxidase (1.4.3.3) · CPC title
Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture · CPC title
Alpha- or beta- amino acids {(other amino acids C12P13/005)} · CPC title
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