Metathesis transformations of microbially-produced fatty acids and fatty acid derivatives
View Patent ↗Methods of producing olefins, bifunctional molecules, and 7-tetradecene are provided. In some embodiments, the methods comprise subjecting a omega-7-olefinic fatty acid or derivative thereof to metathesis transformation, wherein the omega-7-olefinic fatty acid or derivative thereof was produced in a genetically engineered microorganism.
1. A method of producing an olefin comprising contacting a composition comprising at least one omega-7-olefinic fatty acid or derivative thereof with a cross metathesis catalyst under conditions allowing a cross metathesis transformation, wherein the at least one omega-7-olefinic fatty acid or derivative thereof was produced in a genetically engineered microorganism.
2. The method of claim 1 , wherein the omega-7-olefinic fatty acid or derivative thereof has the structure:
wherein n is an integer from 1 to 7, and R1 is selected from methyl ester, ethyl ester, wax ester, amine, amide, carboxylic acid, alcohol, alkane, and aldehyde.
3. The method of claim 1 for producing 7-tetradecene.
4. The method of claim 1 , for producing 1-octene comprising contacting a composition comprising a omega-7-olefinic fatty acid or derivative thereof with a cross metathesis catalyst and ethylene under conditions allowing a metathesis transformation, wherein the fatty acid derivatives have a fraction of modern carbon of about 1.003 to about 1.5.
5. An olefin produced by cross-metathesis according to the method of claim 1 , wherein said olefin has a fraction of modern carbon of about 1.003 to about 1.5.
6. A method of producing a bifunctional molecule, wherein the bifunctional molecule comprises a first terminal functional group and a second terminal functional group, comprising contacting a composition comprising a first olefin and an additional compound with a metathesis catalyst under conditions allowing a cross metathesis transformation, wherein the first olefin comprises a first terminal functional group, wherein the first olefin is a omega-7-olefinic fatty acid or derivative thereof that was produced in a genetically engineered microorganism.
7. The method of claim 6 , wherein the first terminal functional group and the second terminal functional group are independently selected from methyl ester, ethyl ester, wax ester, amine, amide, carboxylic acid, alcohol, alkane, and aldehyde.
8. The method of claim 7 , wherein the first terminal functional group and the second terminal functional group are different.
9. The method of claim 7 , wherein the first terminal functional group and the second terminal functional group are the same.
10. The method of claim 9 , wherein the additional compound is a second olefin.
11. The method of claim 10 , wherein the first olefin and the second olefin are each independently an omega-7-olefinic fatty acid or derivative thereof with the structure:
wherein n is an integer from 1 to 7, and RI is selected from methyl ester, ethyl ester, wax ester, amine, amide, carboxylic acid, alcohol, alkane- and aldehyde.
12. The method of claim 6 , wherein the bifunctional molecule comprises a terminal olefin as the second terminal functional group, wherein said first olefin is a omega-7-olefinic fatty acid or derivative thereof and said additional compound is ethylene.
13. The method of claim 12 , wherein the terminal functional group is selected from methyl ester, ethyl ester, wax ester, amine, amide, carboxylic acid, alcohol, alkane and aldehyde.