Genetically modified host cells and use of same for producing isoprenoid compounds
View Patent ↗The present invention provides genetically modified eukaryotic host cells that produce isoprenoid precursors or isoprenoid compounds. A subject genetically modified host cell comprises increased activity levels of one or more of mevalonate pathway enzymes, increased levels of prenyltransferase activity, and decreased levels of squalene synthase activity. Methods are provided for the production of an isoprenoid compound or an isoprenoid precursor in a subject genetically modified eukaryotic host cell. The methods generally involve culturing a subject genetically modified host cell under conditions that promote production of high levels of an isoprenoid or isoprenoid precursor compound.
1. An isolated eukaryotic host cell comprising one or more heterologous nucleic acids that are integrated into the host cell's chromosome wherein the chromosomally integrated heterologous nucleic acids encode:
a) an enzyme that converts 3-hydroxy-3-methylglutaryl coenzyme-A (HMG-CoA) to mevalonate;
b) farnesyl diphosphate (FPP) synthase; and
c) a repressible promoter that controls transcription of the endogenous gene encoding squalene synthase;
wherein the host cell further comprises a heterologous terpene synthase,
wherein the terpene synthase catalyzes conversion of FPP, produced by action of the FPP synthase, into an isoprenoid, and produces the isoprenoid under culture conditions that provide for repression of transcription of the endogenous squalene synthase-encoding gene,
and wherein FPP does not accumulate at levels that are toxic to the cell.
2. The host cell of claim 1 wherein the enzyme that converts HMG-CoA to mevalonate is a 3-hydroxy-3-methylglutaryl coenzyme-A reductase (HMGR).
3. The host cell of claim 1 wherein the enzyme that converts HMG-CoA to mevalonate is a truncated HMGR.
4. The host cell of claim 1 wherein expression of the enzyme that converts HMG-CoA to mevalonate is under inducible control.
5. The host cell of claim 4 wherein expression of the enzyme that converts HMG-CoA to mevalonate is under the control of a GAL1 promoter.
6. The host cell of claim 1 wherein the enzyme that converts HMG-CoA to mevalonate is under constitutive control.
7. The host cell of claim 1 wherein expression of the FPP synthase is under inducible control.
8. The host cell of claim 7 wherein expression of the FPP synthase is under the control of a GAL1 promoter.
9. The host cell of claim 1 wherein expression of the FPP synthase is under constitutive control.
10. The host cell of claim 1 wherein the repressible promoter is a MET3 promoter.
11. The host cell of claim 1 wherein the repressible promoter is repressed with copper.
12. The host cell of claim 1 wherein the terpene synthase is selected from amorpha-4,11-diene synthase; beta-caryophyllene synthase; germacrene A synthase; 8-epicedrol synthase; valencene synthase; (+)-delta-cadinene synthase; germacrene C synthase; (E)-beta-farnesene synthase; vetispiradiene synthase; 5-epi-aristolochene synthase; aristolchene synthase alpha-humulene synthase; (E,E)-alpha-farnesene synthase; E-alpha-bisabolene synthase; (E)-gamma-bisabolene synthase; longifolene synthase, gamma-humulene synthase, Delta-selinene synthase, epi-cedrol synthase; alpha-zingiberene synthase; guaiadiene synthase; cascarilladiene synthase; cis-muuroladiene synthase; and patchoulol synthase.
13. The cell of claim 1 wherein the isoprenoid is a sesquiterpene.
14. A Saccharomyces cerevisiae cell comprising one or more heterologous nucleic acids that are integrated into the cell's chromosome wherein the chromosomally integrated heterologous nucleic acids encode:
a) a truncated 3-hydroxy-3-methylglutaryl coenzyme-A reductase (HMGR);
b) farnesyl diphosphate (FPP) synthase; and
c) a repressible promoter that controls transcription of the endogenous gene encoding squalene synthase;
wherein the host cell further comprises a heterologous terpene synthase,
wherein the terpene synthase catalyzes conversion of FPP, produced by action of the FPP synthase, into an isoprenoid, and produces the isoprenoid under culture conditions that provide for repression of transcription of the endogenous squalene synthase-encoding gene,
and wherein FPP does not accumulate at levels that are toxic to the cell.
15. The cell of claim 14 wherein the isoprenoid is a sesquiterpene.
16. The host cell of claim 14 , wherein expression of the HMGR is under inducible control.
17. The host cell of claim 16 , wherein expression of the HMGR is under the control of a GAL1 promoter.
18. The host cell of claim 14 , wherein expression of the FPP synthase is under inducible control.
19. The host cell of claim 18 , wherein expression of the FPP synthase transferase is under the control of a GAL1 promoter.
20. The host cell of claim 14 , wherein expression of the FPP synthase is under constitutive control.
21. The host cell of claim 14 , wherein the repressible promoter is a MET3 promoter.
22. The host cell of claim 14 , wherein the terpene synthase is selected from amorpha-4,11-diene synthase; beta-caryophyllene synthase; germacrene A synthase; 8-epicedrol synthase; valencene synthase; (+)-delta-cadinene synthase; germacrene C synthase; (E)-beta-farnesene synthase; vetispiradiene synthase; 5-epi-aristolochene synthase; aristolchene synthase alpha-humulene synthase; (E,E)-alpha-farnesene synthase; E-alpha-bisabolene synthase; (E)-gamma-bisabolene synthase; longifolene synthase, gamma-humulene synthase, Delta-selinene synthase, epi-cedrol synthase; alpha-zingiberene synthase; guaiadiene synthase; cascarilladiene synthase; cis-muuroladiene synthase; and patchoulol synthase.