Materials and methods for using an acyl-acyl carrier protein thioesterase and mutants and chimeras thereof in fatty acid synthesis
View Patent ↗A method of increasing production of fatty acids comprising introducing into a host and expressing therein an acyl-acyl carrier protein (ACP) thioesterase (TE) from Bryantella formatexigens or a mutant thereof; a method of making a mutant B. formatexigens acyl-ACP TE; a method of making a chimeric Cuphea viscosissima acyl-ACP TE; a nucleic acid molecule comprising a nucleotide sequence encoding a mutant acyl-ACP TE or a chimeric Cuphea viscosissima acyl-ACP TE; a host comprising the nucleic acid molecule; a mutant acyl-ACP TE or chimeric Cuphea viscosissima acyl-ACP TE; a method of altering the specificity of a plant acyl-ACP TE for at least one of its substrates comprising introducing into the plant acyl-ACP TE a substrate specificity-altering mutation; and a method of altering the level of activity of a plant acyl-ACP TE.
1. A method of altering the specificity of a plant acyl-ACP TE for at least one of its substrates, which method comprises:
introducing into the plant acyl-ACP TE, the amino acid sequence of which is at least 85% identical to the amino acid sequence of SEQ ID NO:3, a mutation of at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 133, amino acid 139, amino acid 142, and amino acid 143 of SEQ ID NO:3, alone or in further combination with a mutation of at least one amino acid in the region corresponding to amino acids 73-85 of SEQ ID NO:3,
wherein SEQ ID NO:3 is the mature amino acid sequence of the Cuphea viscosissima acyl-ACP TE encoded by the FatB2 gene,
whereupon the specificity of the plant acyl-ACP TE for at least one of its substrates is altered.
2. The method of claim 1 , which further comprises mutating at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 110 and amino acid 184 of SEQ ID NO:3.
3. The method of claim 1 , which further comprises altering the level of activity of the plant acyl-ACP TE by a method comprising mutating at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 173, amino acid 176, and amino acid 205 of SEQ ID NO:3, whereupon the level of activity of the plant acyl-ACP TE is altered.
4. The method of claim 2 , which further comprises altering the level of activity of the plant acyl-ACP TE by a method comprising mutating at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 173, amino acid 176, and amino acid 205 of SEQ ID NO:3, whereupon the level of activity of the plant acyl-ACP TE is altered.
5. A method of altering the level of activity of a plant acyl-ACP TE and the specificity of the plant acyl-ACP TE for at least one of its substrates, which method comprises:
(i) mutating at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 173, amino acid 176, and amino acid 205 of SEQ ID NO:3, and
(ii) introducing into the plant acyl-ACP TE, the amino acid sequence of which is at least 85% identical to the amino acid sequence of SEQ ID NO:3, a mutation of at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 133, amino acid 139, amino acid 142, and amino acid 143 of SEQ ID NO:3, alone or in further combination with a mutation of at least one amino acid in the region corresponding to amino acids 73-85 of SEQ ID NO:3,
wherein SEQ ID NO:3 is the mature amino acid sequence of the Cuphea viscosissima acyl-ACP TE encoded by the FatB2 gene,
whereupon the level of activity of the plant acyl-ACP TE and the specificity of the plant acyl-ACP TE for at least one of its substrates are altered.
6. The method of claim 5 , which further comprises mutating at least one amino acid corresponding to an amino acid selected from the group consisting of amino acid 110 and amino acid 184 of SEQ ID NO:3.