IP Library Granted Patent US 10,655,152
Granted Patent B2
US 10,655,152 · App. 15/513,670 · Granted May 19, 2020

Method for producing an amide

Inventors: Michael Budde (Ilvesheim, DE); Michael Braun (Heidelberg, DE); Juergen Daeuwel (Heidelberg, DE); Peter Oedman (Neustadt, DE); Kai-Uwe Baldenius (Mannheim, DE); Matthias Kleiner (Goennheim, DE); Stephan Freyer (Neustadt, DE)
Assignee: SOLENIS TECHNOLOGIES, L.P.
C12P13/02C12N9/78C12N9/80C12Y305/01004C12Y305/05001
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Quick Facts
Patent No.
US 10,655,152
App. No.
15/513,670
Granted
May 19, 2020
Kind
B2
Abstract

The present invention relates to means and methods for producing an amide compound from a nitrile compound with less acrylic acid as by-product using a Nitrile hydratase (NHase) and Amidase producing microorganism as biocatalyst. Also provided is an aqueous amide compound obtained by the methods of the invention as well as a composition comprising acrylamide or polyacrylamide as well as a dried microorganism exhibiting a NHase/Amidase activity ratio of at least 400 when being brought into contact with a nitrile compound to convert said nitrile compound into an amide compound.

Claims (34)

1. A method for producing an amide compound from a nitrile compound, the method comprising:

contacting the nitrile compound with a microorganism producing a nitrile hydratase (NHase) and an amidase, wherein the microorganism has been previously pre-treated by drying before the contacting with the nitrile compound, wherein a ratio of a NHase activity to an amidase activity of the microorganism is increased, when compared to a reference microorganism, which is not pre-treated by drying before being contacted with the nitrile compound,

wherein the microorganism is selected from the group consisting of Rhodococcus rhodochrous, Rhodococcus pyridinovorans, Rhodococcus erythropolis, Rhodococcus equi, Rhodococcus ruber , and Rhodococcus opacus,

the amide compound is at least one selected from the group consisting of acrylamide, methacrylamide, acetamide, and nicotinamide,

the nitrile compound is at least one selected from the group consisting of acrylonitrile, methacrylonitrile, acetonitrile, and 3-cyanopyridine, and

wherein the drying has been conducted by spray drying, freeze-drying, heat drying, air drying, vacuum drying, fluidized-bed drying, spray granulation, or a combination thereof.

2. The method of claim 1 , wherein the ratio of the NHase activity to the amidase activity of the microorganism is increased by a factor of at least 1.4, when compared to the reference microorganism.

3. The method of claim 1 , wherein the ratio of the amidase activity to the NHase activity of the microorganism is decreased by a factor of at least 0.7, when compared to the reference microorganism, and wherein the reference microorganism is the microorganism producing a nitrile hydratase (NHase) and an amidase that has not been pre-treated by drying.

4. The method of claim 1 , wherein the microorganism exhibits an NHase/amidase activity ratio of at least 400.

5. A method for producing an amide compound from a nitrile compound, the method comprising:

a) drying a microorganism producing a NHase and an amidase; and

b) contacting the nitrile compound with the microorganism after drying

wherein drying increases a NHase/amidase activity ratio of the microorganism, compared to a reference microorganism, which is not treated by drying, wherein the microorganism is selected from the group consisting of Rhodococcus rhodochrous, Rhodococcus pyridinovorans, Rhodococcus erythropolis, Rhodococcus equi, Rhodococcus ruber , and Rhodococcus opacus,

the amide compound is at least one selected from the group consisting of acrylamide, methacrylamide, acetamide, and nicotinamide,

the nitrile compound is at least one selected from the group consisting of acrylonitrile, methacrylonitrile acetonitrile, and 3-cyanopyridine, and

wherein the drying has been conducted by spray drying, freeze-drying, heat drying, air drying, vacuum drying, fluidized-bed drying, spray granulation, or a combination thereof.

6. The method of claim 1 , further comprising reconstituting the pre-treated microorganism after the drying, wherein the contacting is conducted with a reconstituted microorganism.

7. The method of claim 6 , wherein in the reconstituting, the pre-treated microorganism is suspended in an aqueous composition.

8. The method of claim 1 , wherein the contacting is conducted with the pre-treated microorganism in the form of a powder, granule, or suspension, and/or in the form of a matrix bound microorganism.

9. The method of claim 1 , wherein the microorganism is Rhodococcus rhodochrous or Rhodococcus pyridinovorans.

10. The method of claim 9 , wherein the microorganism is Rhodococcus rhodochrous (NCIMB 41164), Rhodococcus rhodochrous (FERM BP-1478) or Rhodococcus rhodochrous M33.

11. The method of claim 1 , wherein the nitrile compound is acrylonitrile.

12. The method of claim 1 , wherein the amide compound is acrylamide.

13. The method of claim 1 , further comprising:

activating by mixing the dried microorganism with an aqueous solution to obtain an activation mixture, wherein the activation mixture comprises a buffer, and

converting the nitrile compound to the amide compound by contacting the nitrile compound with the activation mixture in a reaction mixture, wherein the reaction mixture comprises the buffer and wherein a ratio of a molar concentration of the buffer in the activation mixture to a molar concentration of the buffer in the reaction mixture is about 2:1 or more.

14. A method for producing a microorganism with an increased NHase/amidase activity ratio, comprising:

drying a microorganism producing a NHase and an amidase, and contacting a nitrile compound with the microorganism after the step of drying,

wherein the microorganism is selected from the group consisting of Rhodococcus rhodochrous, Rhodococcus pyridinovorans, Rhodococcus erythropolis, Rhodococcus equi, Rhodococcus ruber , and Rhodococcus opacus,

and the drying is conducted by spray drying, freeze-drying, heat drying, air drying, vacuum drying, fluidized-bed drying, spray granulation, or a combination thereof.

15. A method for reducing the formation of acrylic acid when producing acrylamide from an acrylnitrile compound, the method comprising contacting acrylonitrile with a microorganism producing a NHase and an amidase obtained by the method of claim 14 .

16. The method of claim 1 , wherein the microorganism producing a NHase and an amidase is not immobilized before being dried.

17. The amide compound obtained by the method of claim 1 , wherein the amide compound is in an aqueous solution.

18. A composition comprising acrylamide or polyacrylamide and a microorganism producing a NHase and an amidase that has been pre-treated by drying, wherein the microorganism exhibits a NHase/amidase activity ratio of at least 400, and/or wherein a ratio of a NHase activity to an amidase activity is increased by a factor of at least 1.7, when compared to a reference microorganism, which is the same microorganism but has not been pretreated by drying, wherein the microorganism is selected from the group consisting of Rhodococcus rhodochrous, Rhodococcus pyridinovorans, Rhodococcus erythropolis, Rhodococcus equi, Rhodococcus ruber , and Rhodococcus opacus , and wherein the drying has been conducted by spray drying, freeze-drying, heat drying, air drying, vacuum drying, fluidized-bed drying, spray granulation, or a combination thereof.

Assignments (12)
SECURITY INTEREST Recorded Nov 14, 2025
From: CHEM-AQUA, INC.; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; NCH CORPORATION; NCH LIFE SCIENCES LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073570/0838 →
RELEASE OF SECURITY INTEREST Recorded Nov 14, 2025
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
To: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 073564/0864 →
SECURITY AGREEMENT (NOTES) Recorded Oct 10, 2025
From: DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073061/0885 →
RELEASE OF 2023 NOTES PATENT SECURITY INTERESTS Recorded Oct 10, 2025
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
To: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 073074/0198 →
SECURITY AGREEMENT (2024 NOTES) Recorded Jun 24, 2024
From: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 067824/0278 →
2023 NOTES PATENT SECURITY AGREEMENT Recorded Jul 7, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE GLOBAL CORPORATION
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 064225/0170 →
SECURITY AGREEMENT (NOTES) Recorded Sep 14, 2022
From: SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A. AS COLLATERAL AGENT
Reel/Frame 061432/0821 →
NOTES SECURITY AGREEMENT Recorded Nov 10, 2021
From: INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 058103/0066 →
TERM LOAN PATENT SECURITY AGREEMENT Recorded Nov 10, 2021
From: INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: GOLDMAN SACHS BANK USA
Reel/Frame 058102/0407 →
ABL PATENT SECURITY AGREEMENT Recorded Nov 10, 2021
From: INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: BANK OF AMERICA, N.A.
Reel/Frame 058102/0122 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2019
From: BASF SE
To: SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 048697/0892 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 22, 2018
From: BUDDE, MICHAEL; BRAUN, MICHAEL; DAEUWEL, JUERGEN; OEDMAN, PETER; BALDENIUS, KAI-UWE; KLEINER, MATTHIAS; FREYER, STEPHAN
To: BASF SE
Reel/Frame 045315/0771 →
Priority Claims (1)
EP 14003378 · Sep 30, 2014 · regional
Continuity (1)
Related Publication 20170247726A1 · Aug 31, 2017