IP Library Granted Patent US 11,273,455
Granted Patent B2
US 11,273,455 · App. 16/312,469 · Granted Mar 15, 2022

Method of dewatering post fermentation fluids

Inventor: Feng Xu (Davis, CA)
Assignee: NOVOZYMES A/S
B04B1/20B04B3/04B04B5/10C12N1/205C12N9/22C12P7/10C12R2001/10C12R2001/125Y02E50/10
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Quick Facts
Patent No.
US 11,273,455
App. No.
16/312,469
Granted
Mar 15, 2022
Kind
B2
Abstract

The present invention relates to a method of dewatering post fermentation fluids in a starch to ethanol process. More particularly the invention relates to use of a nuclease enzyme for separation of whole stillage into an insoluble fraction and a supernatant fraction. In a specific embodiment the present invention relates to a method of dewatering whole stillage comprising the steps of: i) subjecting whole stillage to one or more nuclease enzymes; ii) separating the material into an insoluble fraction and a supernatant fraction.

Claims (21)

1. A method of dewatering whole stillage comprising the steps of:

i) subjecting whole stillage to one or more nuclease enzymes;

ii) separating the material into an insoluble fraction and a supernatant fraction.

2. The method of claim 1 , wherein separation in step ii) is carried out by centrifugation.

3. The method of claim 1 , wherein separation in step ii) is carried out by filtration.

4. The method of claim 1 , wherein the whole stillage is derived from a process of producing a fermentation product.

5. The method of claim 1 , wherein the whole stillage is derived from a process of producing a fermentation product from starch-containing material.

6. The method of claim 5 , wherein the starch-containing material is a cereal.

7. The method of claims 5 , wherein the starch-containing material is selected from the group consisting of corn, wheat, barley, cassava, sorghum, rye and potato, or any combination thereof.

8. The method of claim 7 , wherein the starch-containing material is corn.

9. The method of claim 4 , wherein the fermentation product is an alcohol.

10. The method of claim 1 , wherein the nuclease enzyme(s) used in step i) is(are): (a) phosphodiesterase, (b) polynucleotidase or nucleodepolymerase, (c) endonuclease or exonuclease, or (d) DNAse or RNAse.

11. The method of claim 1 , wherein the nuclease enzyme used in step i) is selected from the group consisting of members of EC 3.1.11.-, EC 3.1.12.-, EC 3.1.13.-, EC 3.1.14.-, EC 3.1.15.-, EC 3.1.16.-, EC 3.1.21.- (such as EC 3.1.21.1 to 4), EC 3.1.22.-, EC 3.1.25.-, EC 3.1.26.-, EC 3.1.27.-, EC 3.1.3.-, EC 3.1.30.-, EC 3.1.31.-, EC 3.1.4.- and EC 3.1.99.-, family, or a mixture thereof.

12. The method of claim 11 , wherein the nuclease enzyme is derived from a bacterium.

13. The method of claim 4 , wherein the fermentation product is ethanol.

14. The method of claim 12 , wherein the bacterium is a strain of Bacillus.

15. The method of claim 14 , wherein the strain is selected from the group consisting of B. subtilis and B licheniformis.

16. The method of claim 12 , wherein the fungus is a strain of Aspergillus.

17. The method of claim 16 , wherein the strain is A. oryzae.

18. The method of claim 12 , wherein the plant is mung bean.

19. The method of claim 12 , wherein the animal source is bovine spleen.

Continuity (2)
Provisional Application 62354903 · Jun 27, 2016
Related Publication 20190126293A1 · May 2, 2019
Cited By (1)
US 12,480,142