LOWERING SATURATED FATTY ACID CONTENT OF PLANT SEEDS
Compositions and methods include genetically encoding and expressing a novel delta-9 desaturase in plant cells. In some embodiments, methods of expressing nucleic acids in a plant cell to take advantage of the delta-9 desaturase enzyme's activity, such that the percent composition of saturated fatty acids in plant seeds is decreased and there is a concomitant increase in ω-7 fatty acids. In other embodiments, amino acid sequences have delta-9 desaturase activity. Methods can involve expression of delta-9 desaturase in plant cells, plant materials, and whole plants for the purpose of increasing the amount of unusual fatty acids in whole plants, plant seeds, and plant materials, for example, seeds.
1 . An isolated nucleic acid molecule encoding a delta-9 desaturase enzyme comprising an amino acid sequence being at least 80% identical to a sequence selected from the group consisting of SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:50, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:72, and SEQ ID NO:73.
2 . The nucleic acid molecule of claim 1 , wherein the nucleic acid molecule comprises a nucleotide sequence at least 60% identical to a sequence selected from the group consisting of SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:44, and SEQ ID NO:45.
3 . The nucleic acid molecule of claim 1 , further comprising a gene regulatory element.
4 . The nucleic acid molecule of claim 3 , wherein the gene regulatory element is selected from the group consisting of the Saccharomyces cerevisiae delta-9 desaturase promoter, the delta-9 desaturase 3′UTR/terminator, the ole1 gene promoter, the phaseolin promoter, the Phaseolus vulgaris phaseolin 5′ untranslated region, the Phaseolus vulgaris phaseolin 3′ untranslated region, the Phaseolus vulgaris phaseolin matrix attachment region, the Agrobacterium tumefaciens ORF23 3′ untranslated region, the Cassava vein Mosaic Virus Promoter, the Agrobacterium tumefaciens ORF1 3′ untranslated region, the Nicotiana tabacum RB7 Matrix Attachment Region, Overdrive, T-stand border sequences, the LfKCS3 promoter, FAE 1 promoter, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43, a Myc tag, and a hemagglutin tag.
5 . An isolated delta-9 desaturase enzyme comprising an amino acid sequence at least 80% identical to a sequence selected from the group consisting of SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:50, SEQ ID NO:51, SEQ ID NO:52, SEQ ID NO:72, and SEQ ID NO:73.
6 . A chimeric delta-9 desaturase polypeptide comprising SEQ ID NO:72 and/or SEQ ID NO:73, wherein the polypeptide further comprises an amino acid sequence selected from the group consisting of SEQ ID NO:77 and SEQ ID NO:78.
7 . A method for decreasing the amount of saturated fatty acids in a cell, the method comprising:
transforming a cell with at least one nucleic acid molecule of claim 1 , such that the amount of saturated fatty acids in the cell is decreased.
8 . The method according to claim 7 , wherein the cell is a yeast cell.
9 . The method according to claim 7 , wherein the cell is a plant cell.
10 . The method according to claim 9 , wherein transforming the plant cell introduces into the plant cell a means for decreasing levels of 16:0-ACP in the plant cell.
11 . The method according to claim 10 , wherein the means for decreasing levels of 16:0-ACP in the plant cell is an extraplastidial desaturase.
12 . The method of claim 11 , wherein the extraplastidial desaturase is a desaturase selected from the group consisting of LnD9DS desaturase, AnD9DS desaturase, HzD9DS desaturase, and MgD9DS desaturase.
13 . The method according to claim 9 , wherein the plant cell is obtained from a plant selected from a genus selected from the group consisting of Arabidopsis, Borago, Canola, Ricinus, Theobroma, Zea, Gossypium, Crambe, Cuphea, Linum, Lesquerella, Limnanthes , Linola, Tropaeolum, Oenothera, Olea, Elaeis, Arachis , rapeseed, Carthamus, Glycine, Soja, Helianthus, Nicotiana, Vernonia, Triticum, Hordeum, Oryza, Avena, Sorghum, Secale , and the other members of the Gramineae.
14 . An oil seed plant comprising the nucleic acid sequence of claim 1 .
15 . A plant seed which expresses an extraplastidial desaturase selected from the group consisting of NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:50, SEQ ID NO:51, and SEQ ID NO:52.
16 . A seed of a transgenic Brassica napus line, the seed having a decreased levels of 16:0, relative to an isogenic version of the transgenic Brassica napus line.
17 . A method for creating a genetically engineered plant comprising decreased amounts of saturated fatty acids in the plant compared to the wild type plant, the method comprising:
transforming plant material with the nucleic acid molecule of claim 1 ; and
culturing the transformed plant material to obtain a plant.
18 . The method of claim 17 , wherein the plant is selected from a genus selected from the group consisting of Arabidopsis, Borago, Canola, Ricinus, Theobroma, Zea, Gossypium, Crambe, Cuphea, Linum, Lesquerella, Limnanthes , Linola, Tropaeolum, Oenothera, Olea, Elaeis, Arachis , rapeseed, Carthamus, Glycine, Soja, Helianthus, Nicotiana, Vernonia, Triticum, Hordeum, Oryza, Avena, Sorghum, Secale , and the other members of the Gramineae.
19 . A plant obtained by the method of claim 17 .
20 . A plant material obtained from the plant of claim 19 .
21 . The plant material of claim 20 , wherein the plant material is a seed.