Methods for accumulating heterologous polypeptides in plant stover utilizing a vacuole sorting signal

• US 8,168,863 B2
• Filed: 01/26/2009
• Issued: 05/01/2012
• Est. Priority Date: 01/30/2008
• Status: Active Grant

• Current Assignee: Syngenta Participations AG (China National Chemical Corporation)
• Original Assignee: Syngenta Participations AG (China National Chemical Corporation)
• Inventors: Miles, Stacy
• Primary Examiner(s): Worley, Cathy Kingdon
• Application Number:
  US12/359,421
• Publication Number:
  US 20090193541A1
• Time in Patent Office: 1,191 Days
• Field of Search: None
• US Class Current: 800/288
• CPC Class Codes: C12N 15/8221 Transit peptides
• CPC Class Codes: C12N 15/8246 Non-starch polysaccharides, e.g. cellulose, fructans, levans
• CPC Class Codes: C12N 15/8257 for the production of primary gene products, e.g. pharmaceutical products, interferon
• 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: C12Y 302/01091 Cellulose 1,4-beta-cellobiosidase (3.2.1.91)

Abstract

Compositions and methods for increasing the expression and/or accumulation of cellobiohydrolase enzyme in the vacuoles of plant cells are provided. The method involves targeting the enzyme to the vacuoles through the use of a barley polyamine oxidase (BPAO) vacuole sorting signal peptide. Plants transformed with an expression construct encoding the vacuole sorting signal peptide operably linked to the cellobiohydrolase enzyme direct expression of the polypeptide to the vacuoles of the plant cells. Transgenic plants, seeds, and plant tissues, and plant parts are provided. Downstream uses of transgenic plants or plant material expressing the constructs of the invention include agronomical and industrial uses, for example, human food, animal feed, biofuel, industrial alcohol, fermentation feedstocks, and the like.

Claims

1. An isolated nucleic acid molecule comprising a protein storage vacuole targeting sequence operably linked to a nucleic acid encoding a cellobiohydrolase (CBH), which is operatively linked to a plant green tissue specific promoter, wherein the protein storage vacuole targeting sequence comprises the amino acid sequence of SEQ ID NO:

2 or SEQ ID NO;

5.

2. The isolated nucleic acid of claim 1, wherein the cellobiohydrolase (CBH) is a protein secreted by a fungus.

3. The isolated nucleic acid of claim 2, wherein the cellobiohydrolase is selected from the group consisting of cellobiohydrolase 1 (CBH1) and cellobiohydrolase 2 (CBH2).

4. The isolated nucleic acid of claim 3, wherein the CBH1 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

11, 15, 19 and 21.

5. The isolated nucleic acid of claim 3, wherein the CBH2 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

13 and 17.

6. A method for accumulating a cellobiohydrolase (CBH) in a transgenic plant comprising the steps of:

a) operatively linking a plant green tissue specific promoter, a protein storage vacuole targeting sequence and a nucleic acid encoding the cellobiohydrolase, wherein the protein storage vacuole targeting sequence comprises the amino acid sequence of SEQ ID NO;

2 or SEQ ID NO;

5; and

b) generating a transgenic plant wherein the cellobiohydrolase is targeted to the vacuole.

7. The method of claim 6, wherein the cellobiohydrolase is a protein secreted by a fungus.

8. The method of claim 7, wherein the cellobiohydrolase is selected from the group consisting of cellobiohydrolase 1 (CBH1) and cellobiohydrolase 2 (CBH2).

9. The method of claim 8, wherein the CBH1 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

11, 15, 19 and 21.

10. The method of claim 8, wherein the CBH2 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

13 and 17.

11. A transgenic plant cell comprising a nucleic acid molecule comprising a polynucleotide encoding a protein storage vacuole targeting sequence operably linked to a nucleic acid encoding a cellobiohydrolase which is operatively linked to a plant green tissue specific promoter, wherein the protein storage vacuole targeting sequence comprises the amino acid sequence of SEQ ID NO:

2 or SEQ ID NO;

5.

12. The transgenic plant cell of claim 11, wherein the plant is a monocot.

13. The transgenic plant cell of claim 11, wherein the plant is a dicot.

14. The transgenic plant cell of claim 11, wherein the cellobiohydrolase is a protein secreted by a fungus.

15. The transgenic plant cell of claim 12, wherein the monocot is maize.

16. The transgenic plant cell of claim 14, wherein the cellobiohydrolase is selected from the group consisting of cellobiohydrolase 1 (CBH1) and cellobiohydrolase 2 (CBH2).

17. The transgenic plant cell of claim 16, wherein the CBH1 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

11, 15, 19 and 21.

18. The transgenic plant cell of claim 16, wherein the CBH2 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

13 and 17.

19. A method for accumulating a cellobiohydrolase (CBH) in plant stover comprising the steps of;

a) introducing into a plant cell a nucleic acid construct comprising a polynucleotide encoding a protein storage vacuole sorting signal sequence and a plant green tissue specific promoter, each of which is operably linked to a nucleotide sequence encoding a cellobiohydrolase, wherein the protein storage vacuole sorting signal sequence comprises the amino acid sequence of SEQ ID NO;

2 or SEQ ID NO;

5;

b) regenerating a transformed plant from said plant cell; and

c) allowing the transformed plant to senesce to form stover, thereby accumulating the cellobiohydrolase in said plant stover.

20. The method of claim 19, wherein the heterologous polypeptide accumulates at least 3 fold more cellobiohydrolase in the stover than in the green tissue, wherein the cellobiohydrolase is measured as an amount of cellobiohydrolase per unit of gram of tissue.

21. The method of claim 19, wherein the stover is maize.

22. The method of claim 19, wherein the cellobiohydrolase is a protein secreted by a fungus.

23. The method of claim 19, wherein the cellobiohydrolase is selected from the group consisting of CBH1 and CBH2.

24. The method of claim 23, wherein the CBH1 comprises a polypeptide selected from the group consisting of the amino acid sequence of SEQ ID NOs:

11, 15, 19 and 21.

25. The method of claim 23, wherein the CBH2 comprises a polypeptide selected from the group consisting of the amino acid sequences of SEQ ID NOs:

13 and 17.

26. The method of any one of claims 19 to 21, 22, and 23 to 25, wherein the polypeptide is stable in senesced tissue for at least 2 to 3 months, at least 3 to 6 months, at least 6 to 9 months, at least 9 months to 1 year or more than 1 year.