Method for glucose production using endoglucanase core protein for improved recovery and reuse of enzyme

• US 8,012,721 B2
• Filed: 03/05/2003
• Issued: 09/06/2011
• Est. Priority Date: 03/15/2002
• Status: Expired due to Fees

• Current Assignee: Iogen Energy Corporation (Iogen Corporation)
• Original Assignee: Iogen Energy Corporation (Iogen Corporation)
• Inventors: White, Theresa C., Wahnon, Daphne, Donaldson, Jennifer, Tolan, Jeffrey S.
• Primary Examiner(s): Ariani; Kade
• Application Number:
  US10/507,618
• Publication Number:
  US 20060008885A1
• Time in Patent Office: 3,107 Days
• Field of Search: None
• US Class Current: 435/105
• CPC Class Codes: C12P 19/02 Monosaccharides 2-ketogulonic acid C12P7/60
• CPC Class Codes: C12P 19/14 produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase , e.g. by cellulase, hemicellulase
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel

Abstract

The present invention pertains to a method of converting cellulose to glucose by treating a pretreated lignocellulosic substrate with an enzyme mixture comprising cellulase enzyme and endoglucanase core proteins, wherein the endoglucanase core proteins are present in the enzyme mixture at an amount relative to all endoglucanases from about 35 wt. % to about 100 wt. % and wherein the endoglucanase cellulase enzymes are present in the enzyme mixture at an amount relative to the amount of CBH and EG enzymes from about 2 wt. % to about 50 wt. %. The pretreated lignocellulosic substrate is selected from the group consisting of agricultural residues, residues after starch or sugar removal, dedicated ethanol crops, forestry products, and pulp and paper products, or combinations thereof.

Claims

1. A method of converting the cellulose within a lingocellulosic substrate to glucose, comprising the steps of:

pretreating a lignocellulosic substrate comprising at least about 10% lignin by chemical action so as to hydrolyze hemicellulose contained therein, thereby producing a chemically pretreated lignocellulosic substrate;

treating said chemically pretreated lignocellulosic substrate with an enzyme mixture comprising cellobiohydrolase (CBH) enzymes, β

-glucosidase enzymes, and endoglucanase (EG) enzymes for a sufficient time and under conditions suitable for converting at least about 65% of the cellulose within said lingocellulosic substrate to glucose, wherein said EG enzymes are present at an amount from about 2 to about 50 wt % relative to total amount of CBH enzymes and EG enzymes present in the enzyme mixture, and wherein from about 35 to about 100 wt % of said EG enzymes is a fungal EGII enzyme catalytic core domain; and

recovering said fungal EGII catalytic core domain following said step of treating,

wherein the lignocellulosic substrate is selected from the group consisting of corn stover, wheat straw, barley straw, soybean stover, oat hulls, rice hulls, sugar cane bagasse, corn fibre, switch grass, miscanthus, cord grass, rye grass, hardwood, softwood, Eucalyptus and sawdust, or combination thereof.

2. The method of claim 1, wherein said EG enzymes are present in said enzyme mixture in an amount from 7 to 30 wt % relative to the total amount of CBH enzymes and EG enzymes present in the enzyme mixture.

3. The method of claim 1, wherein said fungal EGII catalytic core domain is present in said enzyme mixture at from about 50 to about 90 wt % of said EG enzymes.

4. The method of claim 3, wherein said fungal EGII catalytic core domain is present in said enzyme mixture at from about 60 to about 80 wt % of said EG enzymes.

5. The method of claim 1, wherein said fungal EGII catalytic core domain comprises a linker.

6. The method of claim 1, wherein the β

-glucosidase enzymes, in said enzyme mixture are obtained from at least one of Trichoderma, Hypocrea, Thermomonospora, Aspergillus, Streptomyces, Cellulomonas, Humicola, Fusarium, Fibrobacter, Clostridium, or Bacillus.

7. The method of claim 6, wherein the CBH and EG enzymes in said enzyme mixture are obtained from Trichoderma, and said β

-glucosidase enzymes are obtained from Aspergillus or Trichoderma.

8. The method of claim 7, wherein said CBH enzymes and EG enzymes are from Trichoderma reesei.

9. The method of claim 1, wherein said fungal EGII catalytic core domain is reused to hydrolyze cellulose following said step of recovering.

10. The method of claim 1, wherein said lignocellulosic substrate is selected from the group consisting of corn stover, wheat straw, barley straw, and soybean stover.

11. The method of claim 1, wherein the pretreated lignocellulosic substrate is present at a concentration of about 1 to about 25 wt % when treated with said enzyme mixture.

12. The method of claim 10, wherein said lignocellulosic substrate is present at a concentration of about 10 to about 16 wt % when treated with said enzyme mixture.

13. The method of claim 1, wherein said step of recovering comprises precipitating said fungal EGII catalytic core domain, or using an ultrafiltration membrane to recover said fungal EGII catalytic domain from solution.

14. The method of claim 1, wherein said pretreating comprises an acid steam cook.

15. The method of claim 1, wherein said CBH enzymes comprise Cellobiohydrolase I (CBHI) and Cellobiohydrolase II (CBHII).

16. The method of claim 15, wherein CBHI is present from about 25 to about 95 wt % of said CBH enzymes.

17. The method of claim 15, wherein the CBHI is from Trichoderma.

18. The method of claim 15, wherein the CBHII is from Trichoderma.

19. The method of claim 1, wherein said lignocellulosic substrate is selected from the group consisting of oat hulls, rice hulls, sugar cane bagasse and corn fibre.

20. The method of claim 1, wherein said lignocellulosic substrate is selected from the group consisting of switch grass, miscanthus, cord grass and rye grass.

21. The method of claim 1, wherein said lignocellulosic substrate is selected from the group consisting of hardwood, softwood, Eucalyptus and sawdust.