Genetically modified host cells and use of same for producing isoprenoid compounds
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.
Claims
exact text as granted — not AI-modifiedWhat 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 that provide for:
a) an increased level of activity of one or more mevalonate pathway enzymes, b) an increased level of prenyltransferase activity, and c) a decreased level of squalene synthase activity 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 prenyltransferase is farnesyl pyrophosphate synthase.
3 . The genetically modified eukaryotic host cell of claim 1 , wherein the prenyltransferase is geranyl pyrophosphate synthase.
4 . The genetically modified eukaryotic host cell of claim 1 , wherein the prenyltransferase is geranylgeranyl pyrophosphate synthase.
5 . The genetically modified eukaryotic host cell of claim 1 , wherein the genetically modified eukaryotic host cell is a yeast cell.
6 . The genetically modified host cell of claim 5 , wherein the genetically modified eukaryotic host cell is Saccharomyces cerevisiae.
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 truncated hydroxymethylglutaryl coenzyme-A reductase.
8 . 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.
9 . The genetically modified host cell of claim 8 , wherein the level of transcription of hydroxymethylglutaryl coenzyme-A synthase, mevalonate kinase, and phosphomevalonate kinase is increased.
10 . 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
11 . The genetically modified host cell of claim 10 , wherein the level of transcription of hydroxymethylglutaryl coenzyme-A synthase, mevalonate kinase, and phosphomevalonate kinase is increased.
12 . 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, wherein the promoter replaces an endogenous promoter operably linked to an endogenous nucleotide sequence encoding farnesyl pyrophosphate synthase, wherein the heterologous promoter provides for an increased level of farnesyl pyrophosphate synthase compared to a control host cell.
13 . The genetically modified host cell of claim 12 , wherein the heterologous promoter is a GAL1 promoter.
14 . 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, wherein the promoter replaces an endogenous promoter operably linked to an endogenous nucleotide sequence encoding geranyl pyrophosphate synthase, wherein the heterologous promoter provides for an increased level of geranyl pyrophosphate synthase compared to a control host cell.
15 . The genetically modified host cell of claim 14 , wherein the heterologous promoter is a GAL1 promoter.
16 . 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, wherein the promoter replaces an endogenous promoter operably linked to an endogenous nucleotide sequence encoding geranylgeranyl pyrophosphate synthase, wherein the heterologous promoter provides for an increased level of geranylgeranyl pyrophosphate synthase compared to a control host cell.
17 . The genetically modified host cell of claim 16 , wherein the heterologous promoter is a GAL1 promoter.
18 . 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.
19 . The genetically modified host cell of claim 1 , wherein the genetically modified host cell is further genetically modified with a nucleic acid comprising a nucleotide sequence encoding a terpene synthase.
20 . The genetically modified host cell of claim 19 , wherein the terpene synthase is selected from amorpha-4,11-diene synthase (ADS), beta-caryophyllene synthase, germacrene A synthase, 8-epicedrol synthase, valencene synthase, (+)-delta-cadinene synthase, germacrene C synthase, (E)-beta-farnesene synthase, Casbene synthase, vetispiradiene synthase, 5-epi-aristolochene synthase, Aristolchene synthase, beta-caryophyllene, alpha-humulene, (E,E)-alpha-farnesene synthase, (−)-beta-pinene synthase, Gamma-terpinene synthase, limonene cyclase, Linalool synthase,1,8-cineole synthase, (+)-sabinene synthase, E-alpha-bisabolene synthase, (+)-bornyl diphosphate synthase, levopimaradiene synthase, Abietadiene synthase, isopimaradiene synthase, (E)-gamma-bisabolene synthase, taxadiene synthase, copalyl pyrophosphate synthase, kaurene synthase, longifolene synthase, gamma-humulene synthase, Delta-selinene synthase, beta-phellandrene synthase, limonene synthase, myrcene synthase, terpinolene synthase, (−)-camphene synthase, (+)-3-carene synthase, syn-copalyl diphosphate synthase, alpha-terpineol synthase, syn-pimara-7,15-diene synthase, ent-sandaaracopimaradiene synthase, sterner-13-ene synthase, E-beta-ocimene, S-linalool synthase, geraniol synthase, gamma-terpinene synthase, linalool synthase, E-beta-ocimene synthase, epi-cedrol synthase, alpha-zingiberene synthase, guaiadiene synthase, cascarilladiene synthase, cis-muuroladiene synthase, aphidicolan-16b-ol synthase, elizabethatriene synthase, sandalol synthase, patchoulol synthase, Zinzanol synthase, cedrol synthase, scareol synthase, copalol synthase, and manool synthase.
21 . The genetically modified host cell of claim 19 , wherein the terpene synthase is amorpha-4,11-diene synthase.
22 . 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.
23 . The method of claim 22 , wherein the conditions comprise inclusion in the culture medium of an inducing agent that activates an inducible promoter.
24 . The method of claim 22 , wherein the isoprenoid compound is a monoterpene.
25 . The method of claim 22 , wherein the isoprenoid is a polyterpene.
26 . The method of claim 22 , wherein the isoprenoid is a diterpene.
27 . The method of claim 22 , wherein the isoprenoid is a triterpene.
28 . The method of claim 22 , wherein the isoprenoid is a carotenoid.
29 . The method of claim 22 , wherein the isoprenoid is a sesquiterpene.
30 . The method of claim 29 , wherein the sesquiterpene is amorphadiene.Join the waitlist — get patent alerts
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