Energy crops for improved biofuel feedstocks

• US 8,237,014 B2
• Filed: 02/27/2007
• Issued: 08/07/2012
• Est. Priority Date: 02/27/2006
• Status: Expired due to Fees

• Current Assignee: Edenspace Systems Corporation
• Original Assignee: Edenspace Systems Corporation
• Inventors: Blaylock, Michael J., Ferguson, Bruce W., Lee, David A.
• Primary Examiner(s): Page, Brent T
• Application Number:
  US11/712,593
• Publication Number:
  US 20070250961A1
• Time in Patent Office: 1,988 Days
• Field of Search: None
• US Class Current: 800/278
• 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: C12N 15/8255 involving lignin biosynthesis
• CPC Class Codes: C12N 15/8261 with agronomic (input) traits, e.g. crop yield
• CPC Class Codes: C12N 9/2437 Cellulases (3.2.1.4; 3.2.1.74; 3.2.1.91; 3.2.1.150)
• CPC Class Codes: C12P 7/08 produced as by-product or from waste or cellulosic material substrate
• CPC Class Codes: C12Y 302/01004 Cellulase (3.2.1.4), i.e. endo-1,4-beta-glucanase
• CPC Class Codes: Y02A 40/146 Genetically Modified [GMO] plants, e.g. transgenic plants
• 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 enzymes, and simplification of harvesting and downstream processing. Also provided are methods for using these transgenic plants in the production of clean, marketable feedstocks for production of renewable fuels and chemicals and in other applications including phytoremediation.

Claims

1. A method of saccharification comprising steps of:

treating a plant part obtained from at least one transgenic plant with at least one thermostable lignocellulolytic enzyme, wherein the thermostable lignocellulolytic enzyme is expressed from a transgene present in the at least one transgenic plant, under conditions to activate the at least one thermostable lignocellulolytic enzyme thereby deconstructing lignocellulose to form a hydrolysate mixture; and

incubating the hydrolysate mixture under conditions that promote conversion of fermentable sugars of the hydrolysate mixture,

wherein the genome of the at least one transgenic plant is augmented with;

a recombinant polynucleotide encoding the at least one thermostable lignocellulolytic enzyme operably linked to a promoter sequence,

wherein the at least one thermostable lignocellulolytic enzyme exhibits optimal activity at a temperature greater than about 50°

C.,

wherein the at least one thermostable lignocellulolytic enzyme is produced at a level greater than 0.5% total soluble protein, greater than 5% total protein, greater than 10% total soluble protein, or greater than 20% total soluble protein, and

wherein, prior to the treating step, the plant part is not pretreated or is pretreated under conditions of less heat or less acid, or that are otherwise less harsh or produce fewer toxic by-products than conditions used in pretreatment of biomass from non-transgenic plants.

2. The method of claim 1, wherein the plant part is substantially free of soil dirt.

3. The method of claim 1, wherein the plant part is pretreated by heating the plant part to a temperature greater than 50°

C., greater than 75°

C. or greater than 100°

C.

4. The method of claim 1, wherein the plant part is pretreated by adding water to the hydrolysate mixture.

5. The method of claim 1, wherein the plant part is pretreated by chopping, grinding, shredding or pulverizing the plant part.

6. The method of claim 1 further comprising adding external lignocellulolytic enzymes to the plant part prior to the treating step.

7. The method of claim 1, wherein the method results in increased sugar or ethanol production compared to a method in which the plant part is obtained from a non-transgenic plant.

8. The method of claim 1 further comprising removing at least one unfermentable component from the hydrolysate.

9. The method of claim 8, wherein removing the at least one unfermentable component speeds up conversion of fermentable sugars.

10. The method of claim 8, wherein the at least one unfermentable component is selected from the group consisting of lignin, lignin-breakdown products, phenols, furans, and combinations thereof.

11. The method of claim 8, wherein removing the at least one unfermentable component from the hydrolysate mixture comprises separating/isolating and purifying the at least one unfermentable component.

12. The method of claim 10, wherein the at least one unfermentable component is phenol.

13. The method of claim 8, wherein the at least one unfermentable component, or a derivative thereof, is burned to produce heat or electricity.

14. The method of claim 13, wherein the heat produced is used in said method.

15. The method of claim 1 further comprising a step of:

distilling the ethanol produced by conversion of fermentable sugars of the hydrolysate mixture so as to obtain distilled ethanol.

16. The method of claim 15, wherein at least one unfermentable component is added to distilled ethanol as a denaturant.

17. The method of claim 15, wherein at least one unfermentable component is added to ethanol produced by conversion of fermentable sugars of the hydrolysate mixture prior to the distilling step, is distilled with the ethanol, and remains in the distilled ethanol as a denaturant.

18. The method of claim 15, wherein at least one unfermentable component is processed into one or more compounds that can be used as denaturants.

19. The method of claim 18, wherein the one or more compounds that can be used as denaturants comprise alcohols.

20. The method of claim 19, wherein the one or more compounds that can be used as denaturants are selected from the group consisting of methanol and butanol.

21. The method of claim 1, wherein the distilled ethanol comprises one or more unfermentable components that act as denaturants.

22. The method of claim 15, wherein the method further produces a by-product that has higher food value than a by-product produced in a method using a plant part obtained from a non-transgenic plant.

23. The method of claim 22, wherein the by-product comprises dried distillers grain (DDG) that has increased levels of protein or oil, resulting from hydrolysis or removal of cellulose or hemicellulose or breakdown or removal of lignin.

24. The method of any one of claim 1 or 15 further comprising adding microorganisms to the plant part so as to induce simultaneous saccharification and fermentation.

25. The method of claim 24, wherein the microorganisms ferment six-carbon sugars or five-carbon sugars or both.

26. The method of any one of claim 1 or 15, wherein the step of incubating the hydrolysate mixture under conditions that promote conversion of fermentable sugars of the hydrolysate mixture comprises adding microorganisms to the hydrolysate mixture.

27. The method of claim 26, wherein the microorganisms ferment six-carbon sugars or five-carbon sugars or both.

28. The method of claim 1, wherein the plant part comprises plant parts obtained from two or more transgenic plants, wherein the transgenic plants are of the same or different species and produce the same or different lignocellulolytic enzymes.

29. The method of claim 28, wherein the plant parts are co-processed so as to combine the lignocellulolytic enzymes in a desired proportion to increase yield.

30. The method of claim 29, wherein the plant parts are co-processed so as to combine the lignocellulolytic enzymes in a desired proportion to increase yield by achieving more efficient hydrolysis of polysaccharides and breakdown and removal of lignin.

31. The method of claim 1 wherein the plant part comprises plant parts obtained from at least one transgenic plant and plant parts obtained from a non-transgenic plant, and the method is carried out using common equipment and facilities for harvesting, ensilement, chopping, crushing, milling, liquefaction, saccharification, fermentation, distillation, drying, storage or transportation.

32. The method of claim 1, wherein the plant part is selected from the group consisting of corn grain, corn stover, and combinations thereof.

33. The method of claim 1, wherein the genome of the transgenic plant is further augmented with one or more yeast genes to promote simultaneous saccharification and fermentation.

34. The method of claim 1 further comprising a step of:

treating the plant part under conditions that promote starch hydrolysis.

35. The method of claim 34, wherein the step of treating the plant part under conditions that promote starch hydrolysis comprises using at least one amylase enzyme.

36. The method of claim 35, wherein the at least one amylase enzyme is selected from the group consisting of glucoamylase, a-amylase, and combinations thereof.

37. The method of claim 34, wherein the step of treating the plant part under conditions to activate the at least one lignocellulolytic enzyme and the step of treating the plant part under conditions to promote starch hydrolysis are performed simultaneously.

38. The method of claim 34, wherein the step of treating the plant part under conditions to activate the at least one lignocellulolytic enzyme and the step of treating the plant part under conditions to promote starch hydrolysis are performed sequentially.

39. The method of claim 34, wherein the method is carried out using common equipment and facilities for harvesting, ensilement, chopping, crushing, milling, liquefaction, saccharification, fermentation, distillation, drying, storage or transportation.

40. The method of claim 34, wherein the plant part comprises plant parts obtained from two or more transgenic plants, wherein the transgenic plants are of the same or different species and produce the same or different lignocellulolytic enzymes.

41. The method of claim 34, wherein the plant part comprises plant parts obtained from at least one transgenic plant and plant parts obtained from a nontransgenic plant.

42. The method of claim 34, wherein the plant part comprises one or more of corn grain, corn fiber and corn stover.

43. The method of claim 34, wherein the plant part comprises corn grain.

44. The method of claim 42, wherein the method is part of a dry milling process.

45. The method of claim 1, wherein the at least one thermostable lignocellulolytic enzyme is selected from the group consisting of a cellulase, a hemicellulase, a ligninase, and combinations thereof.

46. The method of claim 1, wherein the plant part is obtained from at least one transgenic plant, the genome of which is augmented with at least a first recombinant polynucleotide and a second recombinant polynucleotide,

the first recombinant polynucleotide encoding at least a first lignocellulolytic

enzyme operably linked to a first promoter sequence, and

the second recombinant polynucleotide encoding at least a second lignocellulolytic enzyme operably linked to a second promoter sequence,

wherein the first and second lignocellulolytic enzymes are each independently produced at a level greater than 0.5% total soluble protein, greater than 5% total soluble protein, greater than 10% total soluble protein or greater than 20% total soluble protein.

47. The method of claim 46, wherein the lignocellulolytic enzymes are each independently selected from the group consisting of a cellulase, a hemicellulase, a ligninase, and any combination thereof.

48. The method of claim 46, wherein the lignocellulolytic enzymes are each independently selected from the group consisting of a cellobiohydrolase, an endoglucanase, a β

-D-glucosidase, a xylanase, an arabinofuranosidase, an acetyl xylan esterase, a glucuronidase, a mannanase, a galactanase, an arabinase, a lignin peroxidase, a manganese-dependent peroxidase, a hybrid peroxidase, a laccase, and any combination thereof.

49. The method of claim 46, wherein the lignocellulolytic enzymes comprise an endoglucanase and an endoxylanase, an endoglucanase and a glycoside hydrolase, an endoglucanase and a lignin-peroxidase, an endoxylanase and a glycoside hydrolase, an endoxylanase and a lignin-peroxidase or a glycoside hydrolase and a ligninperoxidase.

50. The method of claim 49, wherein the endoglucanase comprises E 1 endo-1,4-β

-glucanase.

51. The method of claim 1, wherein the recombinant polynucleotide comprises a codon optimized polynucleotide encoding E1 endoglucanase, wherein the codon optimized polynucleotide encodes a polypeptide whose sequence comprises the sequence of SEQ ID NO:

4, wherein the codon optimized polynucleotide is optimized for expression in more than one plant.

52. The method of claim 1, wherein the recombinant polynucleotide comprises a codon optimized polynucleotide encoding the family 48 glycoside hydrolase, wherein the codon optimized polynucleotide encodes a polypeptide whose sequence comprises the sequence of SEQ ID NO:

5, wherein the codon optimized polynucleotide is optimized for expression in more than one plant.

53. The method of claim 1, wherein the recombinant polynucleotide comprises a codon optimized polynucleotide encoding family 10 glycoside hydrolase, wherein the codon optimized polynucleotide encodes a polypeptide whose sequence comprises the sequence of SEQ ID NO:

6, wherein the codon optimized polynucleotide is optimized for expression in more than one plant.

54. The method of any one of claim 51, 52 or 53, wherein the codon optimized polynucleotide is optimized for expression in maize, arabidopsis, and tobacco.

55. The method of claim 1, wherein the at least one thermostable lignocellulolytic enzyme is expressed constitutively or tissue-specifically.

56. The method of claim 1, wherein the at least one thermostable lignocellulolytic enzyme is expressed in a targeted sub-cellular compartment or organelle.

57. The method of claim 1, wherein the plant is a monocotyledonous plant.

58. The method of claim 1, wherein the plant is a dicotyledonous plant.

59. The method of claim 1, wherein the plant is a crop plant.

60. 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.

61. The method of claim 1, the genome of which is further augmented with:

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

62. The method of claim 61, wherein the amylase enzyme comprises alpha amylase enzyme or glucoamylase enzyme.

63. The method of claim 1, the genome of which is further augmented with:

a recombinant polynucleotide encoding at least one enzyme for converting hard-to-ferment sugars to more easily fermentable sugars operably linked to a promoter sequence, wherein the polynucleotide is optimized for expression in the plant.

64. The method of claim 63, wherein the enzyme comprises an isomerase that converts xylose to xylulose.

65. The method of claim 1, the genome of which is further altered so as to minimize dispersal of the transgenes through plant reproduction.

66. The method of claim 65, the genome of which is altered so as to introduce male sterility in the plant or to delay plant flowering.

67. The method of claim 1, the genome of which is further altered so as to reduce the amount of one or more forms of lignin in the transgenic plant relative to cellulose and hemicellulose.

68. The method of claim 1, the genome of which is further altered so as to increase the amount of one or more forms of cellulose in the transgenic plant relative to lignin and hemicellulose.

69. The method of claim 1, the genome of which is further altered so as to increase the amount of one or more forms of hemicellulose in the transgenic plant relative to lignin and cellulose.

70. The method of claim 51, wherein the sequence of the codon optimized polynucleotide comprises the sequence of SEQ ID NO:

1.

71. The method of claim 52, wherein the sequence of the codon optimized polynucleotide comprises the sequence of SEQ ID NO:

2.

72. The method of claim 53, wherein the sequence of the codon optimized polynucleotide comprises the sequence of SEQ ID NO:

3.

73. The method of claim 1, wherein one or more unfermentable components is processed into butanol or methanol.