TEMPERING OF CELLULOSIC BIOMASS

• US 20120058523A1
• Filed: 02/17/2010
• Published: 03/08/2012
• Est. Priority Date: 02/17/2009
• Status: Abandoned Application

• Current Assignee: Edenspace Systems Corporation
• Original Assignee: Edenspace Systems Corporation
• Inventors: Pappan, Kirk, Nair, Ramesh, Blaylock, Michael, Chumley, Forrest, Lee, David, Ferguson, Bruce, Corridor, Deisy
• Application Number:
  US13/201,846
• Publication Number:
  US 20120058523A1
• Time in Patent Office: Days
• US Class Current: 435/99
• CPC Class Codes: C12N 15/8245 involving modified carbohydrate or sugar alcohol metabolism, e.g. starch biosynthesis
• CPC Class Codes: C12N 15/8246 Non-starch polysaccharides, e.g. cellulose, fructans, levans
• 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: C12P 7/10 substrate containing cellulosic material
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel

Abstract

The present invention is directed to improved systems and methods for reducing costs and increasing yields of cellulosic ethanol. In particular, the present invention provides plants genetically transformed for increased biomass, expression of lignocellulolytic enzyme polypeptides, and/or simplification of harvesting and downstream processing. Also provided are methods for processing biomass from these transgenic plants that involve less severe and/or less expensive pre-treatment protocols that are typically employed. Such methods allow, among other things, reduced costs associated with externally applied lignocellulolytic enzyme polypeptides.

Claims

1. A method for cost-effective processing of lignocellulosic biomass comprising steps of:

tempering a sample of plant biomass under conditions to promote activation of lignocellulolytic enzyme polypeptides present in the sample of plant biomass;

pretreating the sample under conditions to promote accessibility of celluloses within the lignocellulosic biomass; and

treating the pretreated sample under conditions that promote hydrolysis of cellulose to fermentable sugars,

wherein the sample of plant biomass is obtained from at least one transgenic plant, the genome of which is augmented with;

a recombinant polynucleotide encoding at least one lignocellulolytic enzyme polypeptide operably linked to a promoter sequence, wherein the polynucleotide is optimized for expression in the plant.

2. The method of claim 1, wherein the step of tempering comprises a process selected from the group consisting of ensilement, grinding, pelleting, microwaving, sonication, incubation at a specific temperature, incubation at a specific pH, and combinations thereof.

3. The method of claim 2, wherein the step of tempering comprises incubating the sample at a temperature between about 25°

C. and about 100°

C. for at least 1 hour.

4. The method of claim 3, wherein the step of tempering comprises incubating the sample at about 85°

C. for at least 5 hours.

5. The method of claim 4, wherein the step of tempering comprises incubating the sample at about 85°

C. for at least 24 hours.

6. The method of claim 2, wherein the step of tempering comprises ensiling the sample of plant biomass.

7. The method of claim 6, wherein the sample is ensiled for at least 5 days.

8. The method of claim 7, wherein the sample is ensiled for at least 10 days.

9. The method of claim 8, wherein the sample is ensiled for at least 20 days.

10. The method of claim 6, wherein the sample is ensiled at about 37°

C.

11. The method of claim 6, wherein the sample is ensiled at about 85°

C.

12. The method of claim 1, wherein the sample of plant biomass is in solid form during the step of tempering.

13. The method of claim 1, wherein the sample of plant biomass is in a liquid slurry during the step of tempering.

14. The method of claim 1, wherein the step of treating comprises externally applying an amount of at least one lignocellulolytic enzyme polypeptide.

15. The method of claim 14, wherein the amount of externally applied lignocellulolytic enzyme polypeptide required to achieve a given level of hydrolysis is less than the amount of externally applied lignocellulolytic enzyme polypeptide required to achieve the same level of hydrolysis of comparable lignocellulosic biomass from a plant part that is not obtained from a transgenic plant.

16. The method of claim 14, wherein the step of treating comprises externally applying an amount of at least two lignocellulolytic enzyme polypeptides, wherein the at least two lignocellulolytic enzyme polypeptides together have at least two different enzyme activities.

17. The method of claim 14, wherein the externally applied lignocellulolytic enzyme polypeptide has at least two different enzyme activities.

18. The method of claim 16 or 17, wherein the at least two different enzyme activities are selected from the group consisting of feruloyl esterase, xylanase, alpha-L-arabinofuranosidase, endogalactanase, acetylxylan esterase, beta-xylosidase, xyloglucanase, glucuronoyl esterase, endo-1,5-alpha-L-arabinosidase, pectin methylesterase, endopolygalacturonase, exopolygalacturonase, pectin lyase, pectate lyase, rhamnogalacturonan lyase, pectin acetylesterase, alpha-L-rhamnosidase, mannanase exoglucanase, cellulase, licheninase, laminarinase, beta-(1,3)-(1,4)-glucanase or beta-glucosidase, and combinations thereof.

19. The method of claim 18, wherein the at least two different enzyme activities comprise exoglucanase, endoglucanase, hemicellulase, and beta-glucosidase.

20. The method of claim 14, wherein the at least one externally applied lignocellulolytic enzyme polypeptide is capable of hydrolyzing cellulose to glucose monomers.

21. The methods of claims 1, wherein a greater level of hydrolysis is obtained from the sample of plant biomass obtained from transgenic plant than from a sample of plant biomass from a non-transgenic plant that is processed under the same conditions.

22. The method of claim 1, wherein the promoter sequence is a sequence of a promoter selected from the group consisting of a constitutive promoter, a developmentally-specific promoter, a tissue-specific promoter, and an inducible promoter.

23. The method of claim 22, wherein the promoter sequence is a sequence of a constitutive promoter selected from the group consisting of the act1 promoter and the 35S CMV promoter.

24. The method of claim 1, wherein the lignocellulolytic enzyme polypeptide is expressed in one or more targeted sub-cellular compartments or organelles.

25. The method of claim 24, wherein the one or more targeted sub-cellular compartments or organelles is selected from the group consisting of the apoplast, chloroplast, vacuole, cell wall, endoplasmic reticulum, and combinations thereof.

26. The method of claim 24, wherein the gene encoding the lignocellulolytic enzyme polypeptide is fused to a signal peptide sequence.

27. The method of claim 24, wherein the signal peptide sequence encodes a secretion signal that allows localization to a cell compartment or organelle selected from the group consisting of cytosol, vacuole, nucleus, endoplasmic reticulum, cell wall, mitochondria, apoplast, peroxisomes, and plastid.

28. The method of claim 27, wherein the signal peptide sequence encodes a secretion signal from sea anemone equistatin.

29. The method of claim 27, wherein the signal peptide sequence encodes a secretion signal comprising a KDEL motif

30. The method of claim 24, wherein the lignocellulolytic enzyme polypeptide is expressed in a plant part selected from the group consisting of stems, leaves, grain, cobs, and combinations thereof.

31. The method of claim 1, wherein the plant is selected from the group consisting of corn, switchgrass, sorghum, miscanthus, sugarcane, poplar, pine, wheat, rice, soy, cotton, barley, turf grass, tobacco, bamboo, rape, sugar beet, sunflower, willow, and eucalyptus.

32. The method of claim 31, wherein the plant is a corn plant.

33. The method of claim 31, wherein the plant is a switchgrass plant.

34. The method of claim 31, wherein the plant is a sorghum plant.

35. The method of claim 1, wherein the lignocellulolytic enzyme polypeptide is selected from the group consisting of cellulases, hemicellulases, ligninases, and combinations thereof.

36. The method of claim 1, wherein the lignocellulolytic enzyme polypeptide is selected from the group consisting of cellobiohydrolases, endoglucanases, β

-D-glucosidases, β

-D-glucan gluchydrolases, xylanases, xyloglucanses, β

-xylosidases, arabinofuranosidases, acetyl xylan esterases, glucuronidases, rhamnogalacturonases, polygalacturonases, pectin methyl esterases, mannanases, galactanases, arabinases, lignin peroxidases, manganese-dependent peroxidases, hybrid peroxidases, laccases, ferulic acid esterases, glucuronyl esterases, isomerases, and combinations thereof.

37. The method of claim 36, wherein the lignocellulolytic enzyme polypeptide comprises an endoglucanase.

38. The method of claim 37, wherein the endoglucanase comprises E1 endo-1,4-β

-glucanase.

39. The method of claim 38, wherein the amino acid sequence of the E1 endo-1,4-β

-glucanase comprises the sequence of SEQ ID NO. 1.

40. The method of claim 36, wherein the lignocellulolytic enzyme polypeptide comprises a xylanase.

41. The method of claim 37, wherein the lignocellulolytic enzyme polypeptide comprises Xyn Z.

42. The method of claim 39, wherein the amino acid sequence of the Xyn Z comprises the sequence of SEQ ID NO. 5.

43. The method of claim 1, wherein the step of tempering comprises externally applying an amount of at least one lignocellulolytic enzyme polypeptide.

44. The method of claim 43, wherein the step of tempering comprises externally applying an amount of at least two lignocellulolytic enzyme polypeptides, wherein the at least two lignocellulolytic enzyme polypeptides together have at least two different enzyme activities.

45. The method of claim 1, wherein the step of treatment further comprises adding a crude extract from a sample of plant biomass, wherein the sample is obtained from at least one transgenic plant, the genomic of which is augmented with:

a recombinant polynucleotide encoding at least one lignocellulolytic enzyme polypeptide operably linked to a promoter sequence, wherein the polynucleotide is optimized for expression in the plant,

and wherein the crude extract comprises at least one lignocellulolytic enzyme polypeptide encoded by the recombinant polynucelotide.

46. The method of claim 45, wherein the crude extract comprises at least one lignocellulolytic enzyme fused to an affinity tag.

47. The method of claim 46, where in the affinity tag comprises a tag selected from the group consisting of HAT (histidine affinity tag), FLAG, c-myc, hemagglutinin antigen, and His.

48. The method of claim 1, wherein the sample of plant biomass comprises insoluble fiber.

49. The method of claim 1 or 43, wherein the sample of plant biomass is obtained from the grain of the transgenic plant.