Method for producing fragrant alcohols
This invention relates generally to methods and compositions for producing a sesquiterpene alcohol comprising contacting a sesquiterpene with a p450 polypeptide with monooxygenase activity.
1. A method of producing one or more sesquiterpene alcohol comprising α-sinensol, β-sinensol, α-santalol, β-santalol, α-trans-bergamotol, epi-β-santalol, lancelol or mixtures thereof, the method comprising contacting one or more of α-farnesene, β-farnesene, α-santalene, β-santalene, α-trans-bergamotene, epi-β-santalene, or β-bisabolene with a polypeptide having a P450 monoxygenase activity;
wherein the polypeptide having a P450 monoxygenase activity comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 71 or SEQ ID NO: 73.
2. The method as recited in claim 1 , wherein the sesquiterpene alcohol produced comprises at least 46% of a cis isomer.
3. The method as recited in claim 1 wherein the sesquiterpene alcohol produced comprises greater than 50% of a cis isomer.
4. The method as recited in claim 1 wherein the sesquiterpene alcohol produced comprises at least 72% of a cis isomer.
5. The method as recited in claim 1 wherein the sesquiterpene alcohol produced comprises at least 96% of a cis isomer.
6. The method as recited in claim 1 wherein the sesquiterpene alcohol produced comprises about 100% of a cis isomer.
7. The method as recited in claim 1 , wherein the polypeptide comprises an amino acid sequence having at least 95% sequence identify to SEQ ID NO: 71, or SEQ ID NO: 73.
8. The method as recited in claim 1 , herein the polypeptide comprises an amino acid sequence having at least 98% sequence identify to SEQ ID NO: 71, or SEQ ID NO: 73.
9. The method as recited in claim 1 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 71, or SEQ ID NO: 73.
10. An isolated polypeptide having monooxygenase activity comprising the amino acid sequence of SEQ ID NO: 73.
11. An isolated nucleic acid molecule comprising: i) the nucleic acid sequence of SEQ ID NO: 72; or ii) a nucleic acid molecule that encodes the polypeptide of claim 10 .
12. The method of claim 1 , comprising transforming an isolated host cell with a nucleic acid encoding a polypeptide comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 71 or SEQ ID NO: 73 and culturing the host cell under conditions that allow for the production of the polypeptide.
13. The method of claim 1 , comprising transforming an isolated host cell with a nucleic acid encoding a polypeptide comprising the amino acid sequence-of SEQ ID NO: 71 or SEQ ID NO: 73 and culturing the host cell under conditions that allow for the production of the polypeptide.
14. The method of claim 1 comprising
i) cultivating an isolated cell under conditions suitable to produce a P450 polypeptide having monooxygenase activity wherein the cell:
a) produces an acyclic pyrophosphate terpene precursor;
b) expresses a P450 reductase,
c) expresses one or more polypeptide that has α-farnesene, β-farnesene, α-santalene, β-santalene, α-trans-bergamotene, epi-β-santalene, or β-bisabolene synthase activity and that produces one or more α-farnesene, β-farnesene, α-santalene, β-santalene, α-trans-bergamotene, epi-β-santalene, or β-bisabolene, and
d) expresses the polypeptide having a P450 monoxygenase activity; and
ii) optionally isolating the alcohol from the cell.
15. The method as recited in claim 14 wherein the acyclic pyrophosphate terpene precursor is selected from the group consisting of geranyl-pyrophosphate (GPP), farnesy-diphosphate (FPP) and geranylgeranyl-pyrophosphage (GGPP).
16. The method as recited in claim 15 wherein the acyclic pyrophosphate terpene precursor is FPP.
17. A vector comprising
a) the nucleic acid molecule of claim 11 ; or
b) a nucleic acid encoding a polypeptide having a P450 monoxygenase activity comprising an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 71 or SEQ ID NO: 73.
18. The vector of claim 17 wherein the vector is a prokaryotic vector, viral vector or a eukaryotic vector.
19. The vector of claim 17 , wherein the vector is an expression vector.
20. The method of claim 14 , wherein the cell is a prokaryotic cell.
21. The method of claim 14 , wherein the cell is a bacterial cell.
22. The method of claim 14 , wherein the cell is a eukaryotic cell.
23. The method of claim 22 , wherein the eukaryotic cell is a yeast cell or a plant cell.
24. The method of claim 1 , wherein the sesquiterpene alcohol produced comprises at least 36% of a cis isomer.