IP Library Granted Patent US 10,612,064
Granted Patent B2
US 10,612,064 · App. 15/506,196 · Granted Apr 7, 2020

Production of steviol glycosides in recombinant hosts

Inventors: Helene Lunde Robertson (Horsholm, DK); Iben Nordmark Andersen (Vedbaek, DK); Adam Matthew Takos (Valby, DK); Swee Chuang Lim Hallwyl (Vallensbaek Strand, DK); Francesca Ambri (Hillerod, DK); Manuel Quiros Asensio (Soborg, DK); Michael Dalgaard Mikkelsen (Vaerlose, DK); Jens Houghton-Larsen (Birkerod, DK); Veronique Douchin (Frederiksberg, DK); Jane Dannow Dyekjaer (Copenhagen, DK); Simon Carlsen (Copenhagen, DK); Nina Nicoline Rasmussen (Hvidovre, DK); Esben Halkjaer Hansen (Frederiksberg, DK)
Assignee: Evolva SA
C12P19/56A23L27/36C07H15/256C12N9/0042C12N9/0073C12N9/1085C12N9/88C12N9/90C12N15/52C12Y106/02004C12Y114/13078C12Y114/13079C12Y205/01029C12Y402/03019C12Y505/01013A23V2002/00C07K2319/00
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Quick Facts
Patent No.
US 10,612,064
App. No.
15/506,196
Granted
Apr 7, 2020
Kind
B2
Abstract

The invention relates to recombinant microorganisms and methods for producing steviol glycosides and steviol glycoside precursors.

Claims (60)

1. A recombinant host that produces a steviol glycoside precursor and/or one or more steviol glycosides in a cell culture, comprising:

(a) a gene encoding a polypeptide that synthesizes ent-kaurenoic acid from ent-kaurene;

wherein the polypeptide that synthesizes ent-kaurenoic acid from ent-kaurene comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:54;

(b) a gene encoding a polypeptide that reduces cytochrome P450 complex;

wherein the polypeptide that reduces cytochrome P450 complex comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:22; and

(c) a gene encoding a polypeptide that synthesizes steviol from ent-kaurenoic acid;

wherein the polypeptide that synthesizes steviol from ent-kaurenoic acid comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:82; and further comprising one or more of:

(d) a gene encoding a polypeptide that synthesizes geranylgeranyl pyrophosphate (GGPP) from farnesyl diphosphate (FPP) and isopentenyl diphosphate (IPP);

wherein the polypeptide that synthesizes geranylgeranyl pyrophosphate (GGPP) from farnesyl diphosphate (FPP) and isopentenyl diphosphate (IPP) comprises a polypeptide having at least 95 sequence identity to the amino acid sequence set forth in SEQ ID NO:49;

(e) a gene encoding a polypeptide that synthesizes ent-copalyl diphosphate from GGPP;

wherein the polypeptide that synthesizes ent-copalyl diphosphate from GGPP comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:37; or

(f) a gene encoding a polypeptide that synthesizes ent-kaurene from ent-copalyl diphosphate;

wherein the polypeptide that synthesizes ent-kaurene from ent-copalyl diphosphate comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:6;

wherein at least one of the genes is a recombinant gene; and

wherein the host is a fungal cell.

2. A recombinant host that produces a steviol glycoside precursor in a cell culture, comprising:

(a) a gene encoding a polypeptide that synthesizes ent-kaurenoic acid from ent-kaurene comprising a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:54;

(b) a gene encoding a polypeptide that reduces cytochrome P450 complex comprising a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:22; and

(c) a gene encoding a polypeptide that synthesizes steviol from ent-kaurenoic acid comprising a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:82;

wherein at least one of the genes is a recombinant gene.

3. The recombinant host of claim 2 , further comprising:

(a) a gene encoding a polypeptide that synthesizes geranylgeranyl pyrophosphate (GGPP) from farnesyl diphosphate (FPP) and isopentenyl diphosphate (IPP) comprising a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:49;

(b) a gene encoding a polypeptide that synthesizes ent-copalyl diphosphate from GGPP comprising a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:37; and

(c) a gene encoding a polypeptide that synthesizes ent-kaurene from ent-copalyl pyrophosphate comprising a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:6;

wherein at least one of the genes is a recombinant gene.

4. The recombinant host of claim 1 , wherein the host further comprises a gene encoding an endoplasmic reticulum membrane polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:114; wherein the gene has a copy number of 2 or more and is overexpressed.

5. The recombinant host of claim 4 , wherein an amount of ent-kaurene, ent-kaurenol, ent-kaurenal, and ent-kaurenol glycoside produced by the host is decreased by at least about 10% relative to a corresponding host lacking the gene.

6. The recombinant host of claim 1 , wherein the polypeptide that synthesizes ent-kaurenoic acid from ent-kaurene is a fusion construct.

7. The recombinant host of claim 6 , wherein the fusion construct comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:118.

8. The recombinant host of claim 1 , further comprising:

(a) a gene encoding a polypeptide that glycosylates steviol or a steviol glycoside at its C-13 hydroxyl group thereof;

(b) a gene encoding a polypeptide that beta 1,3 glycosylates the C3′ of the 13-O-glucose, 19-O-glucose, or both 13-O-glucose and 19-O-glucose of a steviol glycoside;

(c) a gene encoding a polypeptide that glycosylates steviol or a steviol glycoside at its C-19 carboxyl group thereof;

(d) a first gene encoding a first polypeptide that beta 1,2 glycosylates the C2′ of the 13-O-glucose, 19-O-glucose, or both 13-O-glucose and 19-O-glucose of a steviol glycoside; and/or

(e) a second gene encoding a second polypeptide that beta 1,2 glycosylates the C2′ of the 13-O-glucose, 19-O-glucose, or both 13-O-glucose and 19-O-glucose of a steviol glycoside;

wherein at least one of the genes is a recombinant gene; and

wherein the host is producing the one or more steviol glycosides.

9. The recombinant host of claim 8 , wherein:

(a) the polypeptide that glycosylates steviol or the steviol glycoside at its C-13 hydroxyl group thereof comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:30;

(b) the polypeptide that beta 1,3 glycosylates the C3′ of the 13-O-glucose, 19-O-glucose, or both 13-O-glucose and 19-O-glucose of the steviol glycoside comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:83;

(c) the polypeptide that glycosylates steviol or the steviol glycoside at its C-19 carboxyl group comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:29;

(d) the first polypeptide that beta 1,2 glycosylates the C2′ of the 13-O-glucose, 19-O-glucose, or both 13-O-glucose and 19-O-glucose of the steviol glycoside comprises a polypeptide having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO:84; and

(e) the second polypeptide that beta 1,2 glycosylates the C2′ of the 13-O-glucose, 19-O-glucose, or both 13-O-glucose and 19-O-glucose of the steviol glycoside comprises a polypeptide having at least 95% identity to the amino acid sequence set forth in SEQ ID NO:86.

10. The recombinant host of claim 1 , wherein the fungal cell comprises a yeast cell.

11. The recombinant host of claim 10 , wherein the yeast cell is a cell from Saccharomyces cerevisiae.

12. The recombinant host of claim 1 , wherein the host is a Yarrowia lipolytica cell.

13. A cell culture, comprising the host of claim 1 and the steviol glycoside precursor or the one or more steviol glycosides produced by the host, the cell culture further comprising:

(a) glucose, fructose, sucrose, xylose, rhamnose, UDP-glucose, UDP-rhamnose, UDP-xylose, and/or N-acetyl-glucosamine; and

(b) supplemental nutrients comprising trace metals, vitamins, salts, YNB, and/or amino acids;

wherein the steviol glycoside precursor or the one or more steviol glycosides is present at a concentration of at least 1 mg/liter of the cell culture;

wherein the cell culture is enriched for the steviol glycoside precursor or the one or more steviol glycosides relative to a steviol glycoside composition from a Stevia plant and has a reduced level of Stevia plant-derived components relative to a plant-derived Stevia extract.

14. A cell lysate from the cell culture comprising the host of claim 1 and the steviol glycoside precursor or the one or more steviol glycosides produced by the host, comprising:

(a) glucose, fructose, sucrose, xylose, rhamnose, UDP-glucose, UDP-rhamnose, UDP-xylose, and/or N-acetyl-glucosamine; and/or

(b) supplemental nutrients comprising trace metals, vitamins, salts, yeast nitrogen base, YNB, and/or amino acids;

wherein the steviol glycoside precursor or the one or more steviol glycosides produced by the host is present at a concentration of at least 1 mg/liter of the cell culture.

15. The recombinant host of claim 8 , wherein the one or more steviol glycosides comprises steviol-13-O-glucoside (13-SMG), steviol-1,2-bioside, steviol-1,3-bioside, steviol-19-O-glucoside (19-SMG), stevioside, 1,3-stevioside, rubusoside, Rebaudioside A (RebA), Rebaudioside B (RebB), Rebaudioside C (RebC), Rebaudioside D (RebD), Rebaudioside E (RebE), Rebaudioside F (RebF), Rebaudioside M (RebM), Rebaudioside Q (RebQ), Rebaudioside I (Rebl), dulcoside A, di-glycosylated steviol, tri-glycosylated steviol, tetra-glycosylated steviol, penta-glycosylated steviol, hexa-glycosylated steviol, hepta-glycosylated steviol, or isomers thereof.

16. The recombinant host of claim 8 , wherein the amount of 13-SMG produced by the host is increased by at least 2-fold relative to a corresponding host lacking the one or more recombinant genes.

17. The recombinant host of claim 8 , wherein a total amount of 13-SMG, steviol-1,2-bioside, rubusoside, RebB, RebA, RebD, and RebM produced by the host is increased by at least about 10% relative to a corresponding host lacking the one or more recombinant genes.

18. A method of producing a steviol glycoside precursor in a cell culture, comprising culturing the recombinant host of claim 1 under conditions in which the genes are expressed, and wherein the steviol glycoside precursor is produced by the recombinant host.

19. A method of producing one or more steviol glycosides in a cell culture, comprising culturing the recombinant host of claim 8 under conditions in which the genes are expressed, and wherein the one or more steviol glycosides are produced by the recombinant host.

Assignments (2)
MERGER Recorded Jun 18, 2024
From: EVOLVA AG
To: DANSTAR FERMENT AG
Reel/Frame 067764/0562 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2017
From: NORDMARK ANDERSEN, IBEN; LUNDE ROBERTSEN, HELENE; TAKOS, ADAM MATTHEW; HALLWYL, SWEE CHUANG LIM; QUIROS ASENSIO, MANUEL; DALGAARD MIKKELSEN, MICHAEL; HOUGHTON-LARSEN, JENS; DOUCHIN, VERONIQUE; DANNOW DYKJAER, JANE; CARLSEN, SIMON; RASMUSSEN, NINA NICOLINE; HALKJAER HANSEN, ESBEN
To: EVOLVA SA
Reel/Frame 042879/0814 →
Continuity (5)
Provisional Application 62048178 · Sep 9, 2014
Provisional Application 62103547 · Jan 14, 2015
Provisional Application 62117396 · Dec 17, 2015
Provisional Application 62148585 · Apr 16, 2015
Related Publication 20170240942A1 · Aug 24, 2017
Cited By (1)
US 12,467,039