Increasing plant oil content by altering a negative regulator of acetyl-coa carboxylase
AssigneeThe Curators of the University of Missouri
InventorsJay Thelen, Matthew Salie
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Abstract
The present invention provides a method and means to change fatty acid and ultimately triacylglycerol production in plants and algae. Methods of the invention comprise the step of altering the activity levels of the committed step for de novo fatty acid biosynthesis, acetyl-CoA carboxylases (ACCase). More specifically, methods of the invention directly enhance the activity of ACCase by down-regulating the biotin/lipoyl attachment domain containing (BADC) genes through biotechnology or selective breeding approaches.
Claims4
A transgenic plant transformed with a recombinant nucleic acid molecule comprising a synthetic RNAi expression cassette that targets endogenous BADC1 gene in said transgenic plant to reduce or eliminate expression of a BADC1 protein encoded by said endogenous BADC1 gene, wherein said synthetic RNAi expression cassette comprises a heterologous promoter operably linked to an inverted repeat of at least 260 bp in size corresponding to a nucleotide sequence encoding said BADC1 protein, wherein said BADC1 protein has at least 95% amino acid sequence identity to SEQ ID NO:
- 1, wherein said BADC1 protein lacks the conserved biotinylation motif and biotinyl lysine residue of a BCCP1 protein, and wherein said transgenic plant exhibits (i) increase in the activity levels of the committed step for de novo fatty acid biosynthesis, acetyl-CoAcarboxylase (ACCase) and (ii) increase in fatty acid and/or triacylglycerol production in said transgenic plant as compared to a control plant of the same species lacking said recombinant nucleic acid molecule and grown under identical growth conditions.
A method of obtaining a transgenic plant comprising:
- (i) transforming plants with a recombinant nucleic acid molecule comprising a synthetic RNAi expression cassette that targets endogenous BADC1 gene in said transgenic plants to reduce or eliminate expression of a BADC1 protein encoded by said endogenous BADC1 gene, wherein said synthetic RNAi expression cassette comprises a heterologous promoter operably linked to an inverted repeat of at least 260 bp in size corresponding to a nucleotide sequence encoding said BADC1 protein, wherein said BADC1 protein has at least 95% amino acid sequence identity to SEQ ID NO:
- 1, and wherein said BADC1 protein lacks the conserved biotinylation motif and biotinyl lysine residue of a BCCP1 protein;
- and
- (ii) selecting a transgenic plant from the transgenic plants of step (i) that exhibits increase in the activity levels of the committed step for de novo fatty acid biosynthesis, acetyl-CoAcarboxylase (ACCase) and (ii) increase in fatty acid and/or triacylglycerol production in said transgenic plant as compared to a control plant of the same species lacking said recombinant nucleic acid molecule and grown under identical growth conditions.
Dependencies are inferred from the claim text.