Recombinant strain producing O-aminobenzoate and fermentative production of aniline from renewable resources via 2-aminobenzoic acid

Patent metadata

Field	Value
Publication number	US-10731187-B2
Application number	US-201515119825-A
Country	US
Kind code	B2
Filing date	Feb 19, 2015
Priority date	Feb 20, 2014
Publication date	Aug 4, 2020
Grant date	Aug 4, 2020

Abstract

The invention provides a recombinant microbial host cell capable of converting a raw material comprising a fermentable carbon substrate to o-aminobenzoate biologically. The invention further provides a method for producing aniline, comprising the steps of: a) producing o-aminobenzoate by fermentation of a raw material comprising at least one fermentable carbon substrate using the recombinant microbial host cell of the capable of converting said raw material comprising at least one fermentable carbon substrate to o-aminobenzoate biologically, wherein said o-aminobenzoate comprises anthranilate anion, b) converting said o-aminobenzoate from said anthranilate anion to anthranilic acid by acid protonation, c) recovering said anthranilic acid by precipitation or by dissolving in an organic solvent, and d) converting said anthranilic acid to aniline by thermal decarboxylation in an organic solvent.

First claim

The invention claimed is:

1. A recombinant microbial host cell capable of converting a raw material comprising a fermentable carbon substrate to o-aminobenzoate biologically,
wherein the microbial host cell is a Corynebacterium strain,
wherein said Corynebacterium strain is Corynebacterium glutamicum,
wherein said fermentable carbon substrate is selected from the group consisting of C-5 monosaccharides, C-6 monosaccharides, disaccharides, and tri-saccharides, and
wherein said Corynebacterium glutamicum has decreased expression of anthranilate phosphoribosyl transferase caused by reduced expression of trpD gene encoding anthranilate phosphoribosyl transferase, wherein said reduced expression is caused by a genetic modification of the trpD gene, and wherein said genetic modification is selected from the group consisting of SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8.

2. A recombinant microbial host cell capable of converting a raw material comprising a fermentable carbon substrate to o-aminobenzoate biologically,
wherein the microbial host cell is a Corynebacterium strain,
wherein said Corynebacterium strain is Corynebacterium glutamicum,
wherein said fermentable carbon substrate is selected from the group consisting of C-5 monosaccharides, C-6 monosaccharides, disaccharides, and tri-saccharides, and
wherein said Corynebacterium glutamicum has decreased expression of chorismate mutase caused by reduced expression of csm gene encoding chorismate mutase, wherein said reduced expression is caused by a genetic modification of the csm gene, wherein said genetic modification is selected from the group consisting of SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, and SEQ ID NO: 16.

3. The recombinant microbial host cell of claim 1 , wherein said Corynebacterium glutamicum further comprises a deletion in hpr gene or ptsG gene expressing phosphoenolpyruvate-phosphotransferase.

4. The recombinant microbial host cell of claim 1 , wherein said raw material is selected from the group consisting of sugar beet, sugar cane, starch-containing plants, lignocellulose, glycerol, and C1-compounds.

5. A method for producing aniline, the method comprising:
a) producing o-aminobenzoate by fermentation of a raw material comprising at least one fermentable carbon substrate using the recombinant microbial host cell of claim 1 , wherein said o-aminobenzoate comprises an anthranilate anion,
b) converting said o-aminobenzoate from said anthranilate anion to anthranilic acid by acid protonation,
c) recovering said anthranilic acid by precipitation or by dissolving in an organic solvent, and
d) converting said anthranilic acid to aniline by thermal decarboxylation in an organic solvent.

6. The method of claim 5 , wherein said fermentation of step a) is a batch fermentation, a fed-batch fermentation, or a continuous fermentation.

7. The method of claim 5 , wherein at least step a) and step b) are run continuously.

8. The method of claim 5 , wherein said recombinant microbial host is removed prior to performing step b) of converting said o-aminobenzoate from said anthranilate anion to anthranilic acid.

9. The method of claim 5 , wherein said acid protonation of step b) is done by adding HCl.

10. The method of claim 5 , wherein in step c) said recovering of said anthranilic acid by precipitation comprises filtration, thereby generating a slurry comprising said recovered anthranilic acid.

11. The method of claim 5 , wherein in step c) said recovering of said anthranilic acid by dissolving in an organic solvent comprises adding said organic solvent to said anthranilic acid such that said anthranilic acid is recovered as a solute in said organic solvent.

12. The method of claim 5 , wherein step c) is followed by washing and drying the recovered anthranilic acid precipitate in advance of performing the thermal decarboxylation of step d).

13. The method of claim 5 , wherein step d) is performed in the presence of a catalyst.

14. The method of claim 5 , wherein following step c) residual anthranilate anion is recovered by adsorption to an ion exchange resin or an active carbon material or a zeolite, followed by desorption of the recovered anthranilate anion.

15. The method according to claim 14 , wherein subsequent to the recovery of the residual anthranilate anion by adsorption following step c), a water stream devoid of the adsorbed anthranilate anion is at least partially re-fed to the fermentation of step a).

16. The recombinant microbial host cell of claim 4 , wherein said raw material comprises a starch-containing plant comprising corn, wheat, rye, or a combination thereof.

17. The recombinant microbial host cell of claim 4 , wherein said raw material comprises a lignocellulose comprising straw, wood, bagasse, or a combination thereof.

18. The recombinant microbial host cell of claim 4 , wherein said raw material comprises a Cl compound comprising CO.

19. The recombinant microbial host cell of claim 1 , wherein said fermentable carbon substrate comprises a C-5 monosaccharide comprising xylose arabinose, or a combination thereof.

20. The recombinant microbial host cell of claim 1 , wherein said fermentable carbon substrate comprises a C-6 monosaccharide comprising glucose, fructose mannose, or a combination thereof.

21. The recombinant microbial host cell of claim 1 , wherein said fermentable carbon substrate comprises a disaccharide comprising saccharose.

22. The recombinant microbial host cell of claim 1 , wherein said fermentable carbon substrate comprises a trisaccharide comprising kestose.

23. The method of claim 8 , wherein said removed recombinant microbial host is re-fed to the fermentation of step a).

24. The method of claim 9 , wherein said HCl is added to a pH of 2.5 to 4.5.

25. The method of claim 24 , wherein said HCl is added to a pH of 3 to 4.

26. The method of claim 10 , wherein said slurry comprising said recovered anthranilic acid is dissolved in an organic solvent.

27. The method of claim 26 , wherein said organic solvent is aniline or 1-dodecanol or a mixture thereof.

28. The method of claim 11 , wherein said organic solvent comprises aniline or 1-dodecanol or a mixture thereof.

29. The method of claim 13 , wherein said catalyst is a zeolite catalyst and wherein the thermal decarboxylation step d) is followed by a further step e) of purifying the aniline.

30. The method of claim 29 , wherein said zeolite catalyst is zeolite H-Y.

31. The method of claim 29 , wherein purifying the aniline comprises distillation.

32. The method of claim 14 , wherein following step c) residual anthranilate anion is recovered by adsorption to a zeolite modified with Fe 3+ or Ca 2+ .

33. The method of claim 14 , further comprising at least partially refeeding said anthranilate anion to step b) for converting said anthranilate anion to anthranilic acid by acid protonation.

34. The method of claim 33 , wherein the zeolite modified with Fe 3+ or Ca 2+ is Fe—Y zeolite.

35. The recombinant microbial host cell of claim 1 , wherein said Corynebacterium glutamicum further comprises a deletion in pepco gene expressing phosphoenolpyruv

Assignees

• Covestro Deutschland Ag

Inventors

• Jaeger Gernot
• Magnus Jorgen
• Moussa Amgad Salah
• Olf Guenter
• Lolli Giulio
• Behnken Swantje
• Youn Jung-Won
• Yalfani Mohammad
• Sprenger Georg

Classifications

• C07C209/68

  from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton · CPC title

• C12Y504/99005

  Chorismate mutase (5.4.99.5) · CPC title

• C12Y204/02018

  Anthranilate phosphoribosyltransferase (2.4.2.18) · CPC title

• C12P13/04

  Alpha- or beta- amino acids {(other amino acids C12P13/005)} · CPC title

• C12P13/02

  Amides, e.g. chloramphenicol {or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes (peptides C12P21/00 or C07K)} · CPC title