Increasing protein yield in plants

Patent metadata

Field	Value
Publication number	US-11390878-B2
Application number	US-201514605504-A
Country	US
Kind code	B2
Filing date	Jan 26, 2015
Priority date	Sep 30, 2011
Publication date	Jul 19, 2022
Grant date	Jul 19, 2022

Abstract

A method of increasing the yield, stability, or both of an acid sensitive protein in a plant is provided. The method comprises introducing a first nucleic acid and a second nucleic acid into the plant, or portion of the plant. The first nucleic acid comprises a first regulatory region active in the plant and operatively linked to a nucleotide sequence encoding the acid sensitive protein. The second nucleic acid comprises a second regulatory region active in the plant and operatively linked to a nucleotide sequence encoding a channel protein, for example but not limited to a proton channel protein. The plant or portion of the plant is incubated under conditions that permit the expression of the nucleic acids, thereby increasing the yield of the acid sensitive protein when compared to the yield of the acid sensitive protein produced in the plant or portion of the plant produced under the same conditions, and in the absence of the proton channel protein.

First claim

What is claimed is:

1. A method of increasing accumulation of a fusion protein in a plant or a portion of the plant, the method comprising:
a) introducing a first nucleic acid comprising a first regulatory region active in the plant and operatively linked to a nucleotide sequence encoding the fusion protein into the plant, or portion of the plant, wherein the fusion protein comprises an (EAAAK) n linker, where n is 1 to 10, and undergoes irreversible conformational change at a pH within the Golgi apparatus of the plant;
b) introducing a second nucleic acid comprising a second regulatory region active in the plant and operatively linked to a nucleotide sequence encoding a proton channel protein, wherein the proton channel protein is M2 or BM2 and wherein the proton channel protein increases the pH within the Golgi apparatus of the plant; and
c) incubating the plant or portion of the plant under conditions that permit the expression of the nucleic acids and accumulation of the fusion protein, wherein accumulation of the fusion protein is increased when compared to accumulation of the fusion protein produced in the plant or portion of the plant produced under the same conditions, and in the absence of the proton channel protein.

2. The method of claim 1 , wherein the first nucleic acid sequence comprises the first regulatory region operatively linked with one or more than one comovirus enhancer, and the nucleotide sequence encoding the fusion protein.

3. The method of claim 2 , wherein the first nucleic acid sequence additionally comprises one or more than one geminivirus amplification element, and wherein a third nucleic acid encoding a geminivirus replicase is introduced into the plant or portion of the plant.

4. The method of claim 2 , wherein the one or more than one comovirus enhancer is a comovirus UTR.

5. The method of claim 4 , wherein the comovirus UTR is a Cowpea Mosaic Virus (CPMV) UTR.

6. The method of claim 1 , wherein the first nucleic acid is transiently expressed in the plant.

7. The method of claim 1 , wherein the first nucleic acid is stably expressed in the plant.

8. The method of claim 1 further comprising a step of
d) harvesting the plant and purifying the fusion protein.

9. The method of claim 1 , wherein n is 2 to 5.

10. The method of claim 1 , wherein the plant or portion of the plant is Nicotiana benthamiana.

Assignees

• Medicago Inc
• Univ Laval

Inventors

• D'Aoust Marc-Andre
• Couture Manon
• Vezina Louis-Philippe
• Michaud Dominique
• Varennes-Jutras Philippe
• Sainsbury Frank

Classifications

• C12N15/8221

  Transit peptides · CPC title

• C12N2800/40

  Systems of functionally co-operating vectors · CPC title

• C12N15/8257

  for the production of primary gene products, e.g. pharmaceutical products, interferon · CPC title

• C12N2830/60

  from viruses · CPC title

• C12N2760/16151

  Methods of production or purification of viral material · CPC title