Methods and materials for biosynthesis of mogroside compounds

Patent metadata

Field	Value
Publication number	US-10662458-B2
Application number	US-201815900557-A
Country	US
Kind code	B2
Filing date	Feb 20, 2018
Priority date	Dec 4, 2012
Publication date	May 26, 2020
Grant date	May 26, 2020

Abstract

The invention relates to methods for producing mogrosides with the aid of enzymes. In particular the invention proposes various biosynthetic pathways useful for mogroside production and enzymes useful for mogroside production are provided. Furthermore, the invention provides recombinant hosts useful in performing the methods of the invention.

First claim

The invention claimed is:

1. A method of producing a mogrol precursor, a mogroside precursor, and/or a mogroside compound in a recombinant host cell, comprising:
(a) a gene encoding a polypeptide capable of catalyzing conversion of oxido-squalene to produce cucurbitadienol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO:1;

(b) a gene encoding a polypeptide capable of catalyzing conversion of dioxido-squalene to produce 24,25 epoxy cucurbitadienol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO:1;

(c) a gene encoding a polypeptide capable of catalyzing hydroxylation of cucurbitadienol to produce 11-hydroxy-cucurbitadienol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by a nucleotide sequence set forth in SEQ ID NO:14;

(d) a gene encoding a polypeptide capable of catalyzing conversion of 11-hydroxy-cucurbitadienol to produce mogrol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by a nucleotide sequence set forth in SEQ ID NO:5;

(e) a gene encoding a polypeptide capable of catalyzing epoxidation of 11-hydroxy-cucurbitadienol to produce 11-hydroxy-24,25 epoxy cucurbitadienol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by a nucleotide sequence set forth in SEQ ID NO:5;

(f) a gene encoding a polypeptide capable of catalyzing conversion of 11-hydroxy-24,25 epoxy cucurbitadienol to produce mogrol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by a nucleotide sequence set forth in SEQ ID NO:5;

(g) a gene encoding a polypeptide capable of catalyzing epoxidation of cucurbitadienol to produce 24,25 epoxy cucurbitadienol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by a nucleotide sequence set forth in SEQ ID NO:5;

(h) a gene encoding a polypeptide capable of catalyzing hydroxylation of 24,25 epoxy cucurbitadienol to produce 11-hydroxy-24,25 epoxy cucurbitadienol;
wherein the polypeptide comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by a nucleotide sequence set forth in SEQ ID NO:14; and/or

(i) a gene encoding a polypeptide capable of beta-1,6-glycosylation of the C2′ position of the 24-O-glucose and/or beta-1,2-glycosylation of the C6′ position of the 3-O-glucose and/or the 24-O-glucose of the glycosylated mogroside compound;
wherein the one or more polypeptides comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by the nucleotide sequence set forth in SEQ ID NO:26;

wherein at least one of the genes is a recombinant gene;
comprising growing the recombinant host cell in a culture medium, under conditions in which the genes are expressed; and
thereby producing the mogrol precursor, the mogroside precursor, and/or the mogroside compound in the recombinant host cell.

2. The method of claim 1 , wherein the recombinant host cell comprises genes recited in items (a), (c), (d), and (i).

3. The method of claim 1 , wherein the recombinant host cell comprises genes recited in items (a), (c), (e), (f), and (i).

4. The method of claim 1 , wherein the recombinant host cell comprises genes recited in items (a), (g), (h), (f), and (i).

5. The method of claim 1 , wherein the recombinant host cell comprises genes recited in items (c), (d), and (i).

6. The method of claim 1 , wherein the recombinant host cell comprises genes recited in items (b), (f), (h), and (i).

7. The method of claim 1 , wherein the recombinant host cell comprises genes recited in items (f), (h), and (i).

8. The method of claim 1 , wherein the recombinant host cell comprises genes recited in item (i).

9. The method of claim 1 , further comprising isolating the produced mogrol precursor, the mogroside precursor, and/or the mogroside compound.

10. The method of claim 1 , wherein the mogrol precursor is oxidosqualene.

11. The method of claim 1 , wherein the mogroside precursor is a tri-glycosylated mogrol.

12. The method of claim 1 , wherein the mogroside compound is a mogroside compound di-glycosylated at C3′ position and tri-glycosylated at C24′.

13. The method of claim 12 , wherein
the mogroside compound di-glycosylated at C3′ position and tri-glycosylated at C24′ position is mogroside V.

14. An in vivo method for transferring a sugar moiety to a mogrol, a glycosylated mogroside compound, or both the mogrol and the glycosylated mogroside compound, comprising contacting the mogrol, the glycosylated mogroside compound, or both the mogrol and the glycosylated mogroside compound with one or more recombinant polypeptides capable of beta 1,6-glycosylation of the C2′ position of the 24-O-glucose and/or beta-1,2-glycosylation of the C6′ position of the 3-O-glucose and/or the 24-O-glucose of the glycosylated mogroside compound and one or more UDP-sugars, under suitable reaction conditions for the transfer of one or more sugar moieties from the one or more UDP-sugars to the mogrol, the glycosylated mogroside compound, or both the mogrol and the glycosylated mogroside compound;
the method comprising growing a recombinant host cell comprising a gene encoding a polypeptide capable of beta-1,6-glycosylation of the C2′ position of the 24-O-glucose and/or beta-1,2-glycosylation of the C6′ position of the 3-O-glucose and/or the 24-O-glucose of the glycosylated mogroside compound;
wherein the one or more polypeptides comprises a polypeptide having at least 90% sequence identity to the amino acid sequence encoded by the nucleotide sequence set forth in SEQ ID NO:26;
wherein at least one of the genes is a recombinant gene, under conditions in which one or more of the genes are expressed;
wherein contacting the mogrol, the mogroside compound glycosylated at C3′ position and tri-glycosylated at C24′ position with the polypeptide comprises contacting the mogroside compound glycosylated at C3′ position and tri-glycosylated at C24′ position with the polypeptide produced by the recombinant host cell;
wherein the recombinant host cell is a microorganism that is a plant cell, a mammalian cell, an insect cell, a fungal cell, an algal cell, or a bacterial cell; and
wherein a mogroside compound is produced in a cell culture broth upon transfer of the sugar moiety.

15. The method of claim 14 , wherein
the UDP-sugar is UDP-glucose, and the mogroside compound di-glycosylated at C3′ position and tri-glycosylated at C24′ position is produced upon transfer of the glucose moiety to the C6′ position of the 3-0-glucose of the mogroside compound glycosylated at C3′ position and tri-glycosylated at C24′ position.

16. The method of claim 14 , wherein the one or more UDP-sugar comprises UDP-glucose.

17. The method of claim 14 , wherein the mogrol is a plant-derived mogrol.

18. A method of producing a mogrol precursor, a mogroside precursor, and/or a mogroside compound, comprising whole cell bioconversion of a plant-derived or a synthetic mogrol precursor or a mogroside precursor in a cell culture medium of a recombinant host cell comprising:
(a) a gene encoding a polypeptide capable of catalyzing conversion of oxido-squalene to produce cucurbitadienol;
wherein the polypeptide

Assignees

• Evolva Sa

Inventors

• Liu Yaoquan
• Hansen Jorgen
• Houghton-Larsen Jens
• Murali Muthuswamy Panchapagesa
• Kumar Sathish
• Rasmussen Nina Nicoline

Classifications

• C12Y504/99033

  Cucurbitadienol synthase (5.4.99.33) · CPC title

• C12N9/90

  Isomerases (5.) · CPC title

• C12P19/18 Primary

  produced by the action of a glycosyl transferase, e.g. alpha-, beta- or gamma-cyclodextrins · CPC title

• C12P33/00

  Preparation of steroids · CPC title

• C12Y303/00

  Hydrolases acting on ether bonds (3.3) · CPC title