Biofuel production methods and compositions

• US 9,309,528 B2
• Filed: 11/21/2007
• Issued: 04/12/2016
• Est. Priority Date: 11/21/2006
• Status: Active Grant

• Current Assignee: Noble Research Institute, LLC
• Original Assignee: The Samuel Roberts Noble Foundation, Inc.
• Inventors: Dixon, Richard A., Chen, Fang, Wang, Zengyu
• Primary Examiner(s): Zhou, Shubo (Joe)
• Assistant Examiner(s): DEVEAU ROSEN, JASON
• Application Number:
  US11/944,217
• Publication Number:
  US 20080274528A1
• Time in Patent Office: 3,065 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: C12N 15/8245 involving modified carbohydrate or sugar alcohol metabolism, e.g. starch biosynthesis
• CPC Class Codes: C12N 15/8255 involving lignin biosynthesis
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel

Abstract

The invention provides methods for increasing the level of fermentable carbohydrates in a biofuel crop plant such as alfalfa or switchgrass, by modification of the lignin biosynthetic pathway. Also provided are plants prepared by the methods of the invention. Methods for processing plant tissue and for producing ethanol by utilizing such plants are also provided.

Claims

1. A transgenic switchgrass plant comprising a selected DNA that down regulates caffeic acid O-methyltransferase (COMT) through inhibition or translation of a COMT gene and reduces lignin biosynthesis in the plant and wherein the plant exhibits an increase in fermentable carbohydrates relative to a plant of the same genotype lacking the selected DNA, wherein the inhibition of transcription or translation is accomplished by expression of a nucleic acid from said selected DNA complementary to all or part of the COMT gene;

wherein the selected DNA comprises SEQ ID NO;

5 or a fragment of at least 100 contiguous nucleotides thereof, or a sequence with at least 95% identity to SEQ ID NO;

5.

2. The transgenic plant of claim 1, further comprising a second selected DNA that down regulates a lignin biosynthesis gene selected from the group consisting of 4-coumarate 3-hydroxylase (C3H), phenylalanine ammonia-lyase (PAL), cinnamate 4-hydroxylase (C4H), hydroxycinnamoyl transferase (HCT), caffeoyl CoA 3-O-methyltransferase (CCoAOMT), cinnamyl alcohol dehydrogenase (CAD), cinnamoyl CoA-reductase (CCR), 4-coumarate-CoA ligase (4CL), monolignol-lignin-specific glycosyltransferase, and aldehyde dehydrogenase (ALDH), wherein down regulation of said lignin biosynthesis gene is accomplished by expression of nucleic acid sequence complementary to all or part of the lignin biosynthesis gene.

3. The transgenic plant of claim 1, wherein the selected DNA is an antisense or RNAi construct.

4. The transgenic plant of claim 3, wherein the antisense of RNAi construct comprises a promoter selected from the group consisting of a developmentally-regulated, organelle-specific, inducible, tissue-specific, constitutive, cell-specific, seed specific, and germination-specific promoter.

6. The transgenic plant of claim 1, further defined as a progeny plant of any generation of an R0 transgenic plant with the selected DNA, wherein the transgenic plant has inherited the selected DNA from the R0 transgenic plant.

7. The transgenic plant of claim 1, wherein at least two lignin biosynthesis genes are down-regulated.

8. The transgenic plant of claim 7, wherein at least three lignin biosynthesis genes are down-regulated.

9. The transgenic plant of claim 8, wherein at least four lignin biosynthesis genes are down-regulated.

10. A seed of the transgenic plant of claim 1, wherein the seed comprises the selected DNA.

11. A transgenic cell of the transgenic plant of claim 1.

20. A method for the producing lignocellulosic biomass, comprising:

(a) obtaining the plant according to claim 1; and

(b) harvesting the lignocellulosic biomass from the plant.

21. A method for producing ethanol comprising:

(a) obtaining lignocellulosic biomass from the switchgrass plant according to claim 1,

(b) treating the biomass to render carbohydrates in the biomass fermentable and wherein at least about 40% of the total carbohydrates present in the biomass are released and fermentable; and

(c) fermenting the carbohydrates to produce ethanol.

22. The method of claim 21, wherein the step of treating the biomass comprises contacting the biomass with a cellulolytic enzyme.

23. The method of claim 22, wherein the biomass is contacted with the cellulolytic enzyme without an acid pretreatment step.

24. The method of claim 22, further comprising pretreating the biomass with an acid prior to contacting the biomass with the cellulolytic enzyme.

25. The method of claim 21, wherein the plant further comprises a second selected DNA that down regulates an enzyme selected from the group consisting of:

4-coumarate 3-hydroxylase (C3H), phenylalanine ammonia-lyase (PAL), cinnamate 4-hydroxylase (C4H), hydroxycinnamoyl transferase (HCT), caffeoyl coA 3-O-methyltransferase (CCoAOMT), cinnamyl alcohol dehydrogenase (CAD), cinnamoyl CoA-reductase (CCR), 4-coumarate-CoA ligase (4CL), monolignol-lignin-specific glycosyltransferase, and aldehyde dehydrogenase (ALDH).

5. The transgenic plant with the selected DNA, further defined as an R0 transgenic plant.

12. A method of increasing the level of one or more fermentable carbohydrates in a switchgrass plant comprising down-regulating a caffeic acid O-methyltransferase (COMT) in the plant through inhibition of transcription or translation of a COMT gene, wherein the inhibition of transcription or translation is accomplished by introducing and expressing a nucleic acid sequence from a selected DNA complementary to all or part of the COMT gene;

wherein the selected DNA comprises SEQ ID NO;

5 or a fragment thereof of at least 100 contiguous nucleotides thereof, or a sequence with at least 95% identity to SEQ ID NO;

5.

13. The method of claim 12, wherein the nucleic acid sequence is in the antisense orientation.

14. The method of claim 12, wherein the fermentable carbohydrate is selected from the group consisting of xylose, arabinose, mannose, glucose, galactose, xyloglucan, arabinoglucan, galacturonan, starch, and cellobiose.

15. The method of claim 12, wherein the nucleic acid sequence is an antisense or RNAi construct.

16. The method of claim 12, further comprising down-regulating at least a first enzyme activity selected from the group consisting of:

4-coumarate 3-hydroxylase (C3H), phenylalanine ammonia-lyase (PAL), cinnamate 4-hydroxylase (C4H), hydroxycinnamoyl transferase (HCT), caffeoyl coA 3-O-methyltransferase (CCoAOMT), cinnamyl alcohol dehydrogenase (CAD), cinnamoyl CoA-reductase (CCR), 4-coumarate-CoA ligase (4CL), monolignol-lignin-specific glycosyltransferase, and aldehyde dehydrogenase (ALDH).

17. The method of claim 16, wherein the down-regulating comprises introducing into the plant a second selected DNA that down-regulates 3-hydroxylase (C3H) and/or hydroxycinnamoyl transferse (HCT).

18. The method of claim 12, wherein introducing the nucleic acid sequence comprises plant breeding.

19. The method of claim 12, wherein introducing the nucleic acid sequence comprises genetic transformation.