Genetically modified host cells and use of same for producing isoprenoid compounds

Patent metadata

Field	Value
Publication number	US-10435717-B2
Application number	US-201715722844-A
Country	US
Kind code	B2
Filing date	Oct 2, 2017
Priority date	Jul 27, 2004
Publication date	Oct 8, 2019
Grant date	Oct 8, 2019

Abstract

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.

First claim

What is claimed is:

1. A genetically modified eukaryotic host cell that produces an isoprenoid or an isoprenoid precursor compound via a mevalonate pathway, the genetically modified eukaryotic host cell comprising genetic modifications comprising:
a) a heterologous nucleic acid, integrated into the host cell's chromosome, encoding an enzyme that converts 3-hydroxy-3-methylglutaryl coenzyme-A (HMG-CoA) to mevalonate;
b) a heterologous nucleic acid, integrated into the host cell's chromosome, encoding a prenyl transferase;
c) a heterologous nucleic acid, integrated into the host cell's chromosome, to decrease the level of activity of squalene synthase; and
d) a heterologous nucleic acid comprising a nucleotide sequence encoding a terpene synthase,
wherein the genetic modifications provide for production of an isoprenoid or an isoprenoid precursor compound at a level that is at least about 50% higher than the level of the isoprenoid or isoprenoid precursor compound in a control cell not comprising the genetic modifications.

2. The genetically modified eukaryotic host cell of claim 1 , wherein the genetically modified eukaryotic host cell is a yeast cell.

3. The genetically modified host cell of claim 2 , wherein the genetically modified eukaryotic host cell is Saccharomyces cerevisiae.

4. The genetically modified host cell of claim 1 , wherein the genetically modified host cell is genetically modified with a nucleic acid comprising a nucleotide sequence encoding enzyme that converts HMG-CoA to mevalonate is a truncated HMG-CoA reductase.

5. The genetically modified host cell of claim 1 , wherein the genetically modified host cell is genetically modified with a nucleic acid comprising a nucleotide sequence encoding a variant Ecm22p transcription factor, which variant has increased transcriptional activation activity compared to wild-type Ecm22p, wherein the level of transcription of one or more mevalonate pathway enzymes is increased.

6. The genetically modified host cell of claim 5 , wherein the level of transcription of hydroxymethylglutaryl coenzyme-A synthase, mevalonate kinase, and phosphomevalonate kinase is increased.

7. The genetically modified host cell of claim 1 , wherein the genetically modified host cell is genetically modified with a nucleic acid comprising a nucleotide sequence encoding a variant Upc2p transcription factor, which variant has increased transcriptional activation activity compared to wild-type Upc2p, wherein the level of transcription of one or more mevalonate pathway enzymes is increased.

8. The genetically modified host cell of claim 7 , wherein the level of transcription of hydroxymethylglutaryl coenzyme-A synthase, mevalonate kinase, and phosphomevalonate kinase is increased.

9. The genetically modified host cell of claim 1 , wherein the genetically modified host cell is genetically modified with a nucleic acid comprising a heterologous promoter, which heterologous promoter replaces an endogenous promoter operably linked to an endogenous nucleotide sequence encoding squalene synthase, wherein the heterologous promoter provides for a reduced level of squalene synthase compared to a control host cell.

10. The genetically modified eukaryotic host cell of claim 1 , wherein expression of the enzyme that converts HMG-CoA to mevalonate is under inducible control.

11. The genetically modified eukaryotic host cell of claim 1 , wherein expression of the enzyme that converts HMG-CoA to mevalonate is under the control of a GAL1 promoter.

12. The genetically modified eukaryotic host cell of claim 1 , wherein expression of the enzyme that converts HMG-CoA to mevalonate is under constitutive control.

13. The genetically modified eukaryotic host cell of claim 1 , wherein expression of the prenyl transferase is under inducible control.

14. The genetically modified eukaryotic host cell of claim 13 , wherein expression of the prenyl transferase is under the control of a GAL1 promoter.

15. The genetically modified eukaryotic host cell of claim 1 , wherein expression of the prenyl transferase is under constitutive control.

16. The genetically modified host cell of claim 1 , wherein the prenyl transferase is geranyl pyrophosphate synthase.

17. A method for enhancing production of an isoprenoid precursor or an isoprenoid via a mevalonate pathway in a host cell, the method comprising culturing the genetically modified eukaryotic host cell of claim 1 in a suitable medium and under conditions that promote production of the isoprenoid or isoprenoid precursor compound, wherein the isoprenoid or an isoprenoid precursor compound is produced at a level that is at least about 50% higher than the level of the isoprenoid or isoprenoid precursor compound in a control cell not comprising the genetic modifications.

18. The method of claim 17 , wherein the conditions comprise inclusion in the culture medium of an inducing agent that activates an inducible promoter.

19. The method of claim 17 , wherein the isoprenoid is a diterpene.

20. The method of claim 4 , wherein the truncated HMG-CoA reductase comprises an amino acid sequence having at least 95% identity to the amino acid sequence set forth in SEQ ID NO:2.

21. The method of claim 5 , wherein the variant Ecmp22 comprises substitution of glycine-to-aspartic acid substitution at amino acid 790.

Assignees

• Univ California

Inventors

• Keasling Jay D
• Kirby James
• Paradise Eric M

Classifications

• C12N15/81

  for yeasts · CPC title

• C12P23/00

  Preparation of compounds containing a cyclohexene ring having an unsaturated side chain containing at least ten carbon atoms bound by conjugated double bonds, e.g. carotenes (containing heterorings C12P17/00) · CPC title

• C12Y101/01034

  Hydroxymethylglutaryl-CoA reductase (NADPH) (1.1.1.34) · CPC title

• C12N9/0006

  acting on CH-OH groups as donors (1.1) · CPC title

• C12Y402/03024

  Amorpha-4,11-diene synthase (4.2.3.24) · CPC title