Modified acyl-ACP desaturase
AssigneeAssociated Universities, Inc.
InventorsEdgar B. Cahoon, John Shanklin, Ylva Lindgvist, Gunter Schneider
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Abstract
Disclosed is a methods for modifying the chain length and double bond positional specificities of a soluble plant fatty acid desaturase. More specifically, the method involves modifying amino acid contact residues in the substrate binding channel of the soluble fatty acid desaturase which contact the fatty acid. Specifically disclosed is the modification of an acyl-ACP desaturase. Amino acid contact residues which lie within the substrate binding channel are identified, and subsequently replaced with different residues to effect the modification of activity.
Claims9
A nucleic acid sequence encoding a mutant acyl-ACP desaturase which is characterized by the ability to catalyze desaturation of a first fatty acid and a second fatty acid, the first and second fatty acids differing in their chain length, the desaturation rates of both the first and second fatty acids differing by no more than about 4-fold, the nucleic acid sequence encoding the mutant acyl-ACP desaturase being characterized by a point mutation at an amino acid contact residue in the substrate binding channel, the nucleic acid sequence being further characterized as having a sufficient degree of amino acid identity with the amino acid sequence of Ricinus communis .DELTA..sup.9 desaturase to enable statistically significant sequence alignment with the Ricinus communis .DELTA..sup.9 desaturase.
A DNA expression construct comprising, in expressible form, a nucleic acid sequence encoding a mutant acyl-ACP desaturase which is characterized by the ability to catalyze desaturation of a first fatty acid and a second fatty acid, the first and second fatty acids differing in their chain length, the desaturation rates of both the first and second fatty acids differing by no more than about 4-fold, the nucleic acid sequence encoding the mutant acyl-ACP desaturase being characterize by a point mutation at an amino acid contact residue in the substrate binding channel, the nucleic acid sequence being further characterized as having a sufficient degree of amino acid identity with the amino acid sequence of Ricinus communis .DELTA..sup.9 desaturase to enable statistically significant sequence alignment with the Ricinus communis .DELTA..sup.9 desaturase.
A cell transformed with a DNA expression construct comprising, in expressible form, a nucleic acid sequence encoding a mutant acyl-ACP desaturase which is characterized by the ability to catalyze desaturation of a first fatty acid and a second fatty acid, the first and second fatty acids differing in their chain length, the desaturation rates of both the first and second fatty acids differing by no more than about 4-fold, the nucleic acid sequence encoding the mutant acyl-ACP desaturase being characterized by a point mutation at an amino acid contact residue in the substrate binding channel, the nucleic acid sequence being further characterized as having a sufficient degree of amino acid identity with the amino acid sequence of Ricinus communis .DELTA..sup.9 desaturase to enable statistically significant sequence alignment with the Ricinus communis .DELTA..sup.9 desaturase.
Dependencies are inferred from the claim text.