Production of isoprenoids
View Patent ↗Methods for producing an isoprenoid are provided. A plurality of bacterial or fungal host cells is obtained. These cells comprise a heterologous nucleic acid encoding one or more enzymes of a mevalonate pathway for making isopentenyl pyrophosphate. Expression of the one or more enzymes is under control of at least one heterologous transcriptional regulator. The mevalonate pathway comprises (i) an enzyme that condenses acetoacetyl-CoA with acetyl-CoA to form HMG-CoA, (ii) an enzyme that converts HMG-CoA to mevalonate, (iii) an enzyme that phosphorylates mevalonate to mevalonate 5-phosphate, (iv) an enzyme that converts mevalonate 5-phosphate to mevalonate 5-pyrophosphate, and (v) an enzyme that converts mevalonate 5-pyrophosphate to isopentenyl pyrophosphate. The host cells are cultured in a medium under conditions that are suboptimal as compared to conditions for the maximum growth rate. Temperature is maintained at a level below that which would provide for a maximum specific growth rate for the host cells.
1. A method for producing an isoprenoid comprising:
(a) obtaining a plurality of bacterial or fungal host cells that comprise a heterologous nucleic acid encoding one or more enzymes of a mevalonate pathway for making isopentenyl pyrophosphate, wherein expression of the one or more enzymes is under control of at least one heterologous transcriptional regulator, and wherein said mevalonate pathway comprises (i) an enzyme that condenses acetoacetyl-CoA with acetyl-CoA to form HMG-CoA; (ii) an enzyme that converts HMG-CoA to mevalonate; (iii) an enzyme that phosphorylates mevalonate to mevalonate 5-phosphate; (iv) an enzyme that converts mevalonate 5-phosphate to mevalonate 5-pyrophosphate; and (v) an enzyme that converts mevalonate 5-pyrophosphate to isopentenyl pyrophosphate; and
(b) culturing the host cells in a medium wherein temperature is maintained at a level which would provide for about 90% or less of a maximum specific growth rate for the plurality of bacterial or fungal host cells.
2. The method of claim 1 , wherein the at least one heterologous transcriptional regulator is inducible.
3. The method of claim 1 , wherein the pathway enzymes are under control of a single transcriptional regulator.
4. The method of claim 1 , wherein the pathway enzymes are under control of a multiple transcriptional regulator.
5. The method of claim 1 , wherein the host cells are Escherichia coli.
6. The method of claim 1 , wherein the host cells are yeast cells.
7. The method of claim 1 , wherein the host cells are Saccharomyces cerevisiae.
8. The method of claim 1 , wherein the pathway comprises a nucleic acid sequence encoding a mevalonate pathway enzyme from a prokaryote having an endogenous mevalonate pathway.
9. The method of claim 8 , wherein the prokaryote is of the genus selected from Enterococcus, Pseudomonas , and Staphyloccoccus.
10. The method of claim 9 , wherein the nucleic acid sequence is selected from acetyl-CoA thiolase, HMG-CoA synthase, HMG-CoA reductase, and mevalonate kinase.
11. The method of claim 8 , wherein the nucleic acid sequence encodes a Class II HMG reductase.
12. The method of claim 1 , wherein the temperature of the medium is at least about 2-20° C. below that which would provide for the maximum specific growth rate.
13. The method of claim 12 , wherein the host cells are cultured at a temperature at least about 5° C. below that which would provide for the maximum specific growth rate.
14. The method of claim 12 , wherein the temperature of the medium is at least about 10° C. below that which would provide for the maximum specific growth rate.
15. The method of claim 1 , wherein the medium comprises a carbon source and the amount of carbon source will provide for about 90% or less of the maximum specific growth rate.
16. The method of claim 15 , wherein the amount of the carbon source will provide for about 75% or less of the maximum specific growth rate.
17. The method of claim 15 , wherein the amount of the carbon source will provide for about 50% or less of the maximum specific growth rate.
18. The method of claim 15 , wherein the amount of the carbon source will provide for about 25% or less of the maximum specific growth rate.
19. The method of claim 15 , wherein the amount of the carbon source will provide for about 75%-10% of the maximum specific growth rate.
20. The method of claim 1 , wherein the medium comprises a nitrogen source present in an amount below that which would provide for about 90% or less of the maximum specific rate.
21. The method of claim 20 , wherein the amount of the nitrogen source will provide for about 75% or less of the maximum specific growth rate.
22. The method of claim 20 , wherein the amount of the nitrogen source will provide for 50% or less of the maximum specific growth rate.
23. The method of claim 20 , wherein the amount of the nitrogen source will provide for about 25% or less of the maximum specific growth rate.
24. The method of claim 20 , wherein the amount of the nitrogen source will provide for about 75%-10% of the maximum specific growth rate.
25. The method of claim 1 , wherein the isoprenoid is produced in an amount greater than about 10 grams per liter of medium.
26. The method of claim 1 , wherein the isoprenoid is produced in an amount greater than about 50 mg per gram of dry cell weight.
27. The method of any one of claims 25 or 26 , where the amount of isoprenoid is produced in less than about 150 hours.
28. The method of any one of claims 25 or 26 , where the amount of isoprenoid is produced in less than about 96 hours.
29. The method of any one of claims 25 or 26 , where the amount of isoprenoid is produced in less than about 72 hours.
30. The method of claim 1 , wherein the isoprenoid is selected from the group consisting of a hemiterpene, monoterpene, diterpene, triterpene, tetraterpene, and polyterpene.
31. The method of claim 1 , wherein the isoprenoid is not a carotenoid.
32. The method of claim 1 , wherein the isoprenoid is a C 5 -C 20 isoprenoid.
33. The method of claim 1 , wherein the isoprenoid is selected from the group consisting of abietadiene, amorphadiene, carene, α-farnesene, β-farnesene, farnesol, geraniol, geranylgeraniol, isoprene, linalool, limonene, myrcene, nerolidol, ocimene, patchoulol, β-pinene, sabinene, γ-terpinene, terpinolene and valencene.