Production of non-caloric sweeteners using engineered whole-cell catalysts

Patent metadata

Field	Value
Publication number	US-10752928-B2
Application number	US-201615566244-A
Country	US
Kind code	B2
Filing date	Apr 14, 2016
Priority date	Apr 14, 2015
Publication date	Aug 25, 2020
Grant date	Aug 25, 2020

Abstract

Disclosed are whole-cell catalysts, methods of making the whole-cell catalysts, and methods of using the whole-cell catalysts to produce steviol glycosides.

First claim

What is claimed is:

1. A whole-cell catalyst composition for the production of a steviol glycoside, the whole-cell catalyst composition comprising a first whole-cell catalyst, said first whole-cell catalyst being a Pichia pastoris host cell transformed by at least one expression cassette such that the host cell comprises:
(a) at least one first nucleotide sequence encoding a HV1-GCW61 fusion protein in which a display polypeptide is fused to the C-terminal of a UDP-glycosyltransferase (UGT) enzyme such that when expressed the UGT enzyme is attached to the surface of the host cell, wherein the first nucleotide sequence comprises a sequence that is at least 80% identical to the sequence set forth in SEQ ID NO: 2; and
(b) at least one second nucleotide sequence encoding an intracellular sucrose synthase (SUS).

2. The whole-cell catalyst composition of claim 1 , wherein the SUS comprises at least one of: an SUS derived from Arabidopsis thaliana , an SUS derived from Vigna radiate.

3. The whole-cell catalyst composition of claim 2 , wherein the SUS comprises at least one of: Arabidopsis sucrose synthase 1; Arabidopsis sucrose synthase 3; and Vigna radiate sucrose synthase (mbSUS1).

4. The whole-cell catalyst composition of claim 1 , wherein the Pichia pastoris host cell is transformed to include five copies of the first nucleotide sequence and two copies of the second nucleotide sequence, wherein the second nucleotide sequence comprises the sequence set forth in SEQ ID NO: 12.

5. The whole-cell catalyst composition of claim 1 , wherein the whole-cell catalyst composition comprises a second whole-cell catalyst, said second whole-cell catalyst being a Pichia pastoris host cell transformed to include four copies of a third nucleotide sequence encoding a UGT76G1-GCW61 fusion protein, wherein the third nucleotide sequence comprises the sequence set forth in SEQ ID NO: 4 and two copies of the second nucleotide sequence, wherein the second nucleotide sequence comprises the sequence set forth in-SEQ ID NO: 12.

6. The whole-cell catalyst composition of claim 1 , wherein the first nucleotide sequence comprises the sequence set forth in SEQ ID NO: 2.

7. A method of producing a desired steviol glycoside from a starting steviol glycoside substrate, the method comprising:
incubating a whole-cell catalyst composition in a culture medium comprising said starting steviol glycoside substrate, sucrose, UDP and/or UDP-glucose for period such that said starting steviol glycoside substrate is converted to the desired steviol glycoside in the culture medium;
wherein the whole-cell catalyst composition comprises a first whole-cell catalyst, said first whole-cell catalyst being a Pichia pastoris host cell transformed by at least one expression cassette such that the host cell comprises:
(a) at least one first nucleotide sequence encoding a HV1-GCW61 fusion protein in which a display polypeptide is fused to the C-terminal of a UDP-glycosyltransferase (UGT) enzyme such that when expressed the UGT enzyme is attached to the surface of the host cell, wherein the first nucleotide sequence comprises a sequence that is at least 80% identical to the sequence set forth in SEQ ID NO: 2; and
(b) at least one second nucleotide sequence encoding an intracellular sucrose synthase (SUS).

8. The method of claim 7 , wherein the first nucleotide sequence comprises the sequence set forth in SEQ ID NO: 2.

9. The method of claim 7 , wherein the SUS comprises at least one of: an SUS derived from Arabidopsis thaliana , an SUS derived from Vigna radiate.

10. The method of claim 9 , wherein the SUS comprises at least one of: Arabidopsis sucrose synthase 1; Arabidopsis sucrose synthase 3; and Vigna radiate sucrose synthase (mbSUS1).

11. The method of claim 7 , wherein the whole-cell catalyst composition comprises a second whole-cell catalyst, said second whole-cell catalyst being a Pichia pastoris host cell transformed to include four copies of a third nucleotide sequence encoding a UGT76G1-GCW61 fusion protein, wherein the third nucleotide sequence comprises the sequence set forth in SEQ ID NO: 4 and two copies of the second nucleotide sequence, wherein the second nucleotide sequence comprises the sequence set forth in-SEQ ID NO: 12.

12. The method of claim 7 , wherein the Pichia pastoris host cell is transformed to include five copies of the first nucleotide sequence and two copies of the second nucleotide sequence, wherein the second nucleotide sequence comprises the sequence set forth in-SEQ ID NO: 12.

13. The method of claim 11 , wherein the starting steviol glycoside substrate is stevioside and the produced steviol glycoside is rebaudioside A.

14. The method of claim 11 , wherein the starting steviol glycoside substrate is rebaudioside D and the produced steviol glycoside is rebaudioside M.

15. The method of claim 11 , wherein the starting steviol glycoside substrate is rebaudioside E and the produced steviol glycoside is rebaudioside D.

16. The method of claim 12 , wherein the starting steviol glycoside substrate is rebaudioside A and the produced steviol glycoside is rebaudioside D.

17. The method of claim 12 , wherein the starting steviol glycoside substrate is stevioside and the produced steviol glycoside is rebaudioside E.

18. The method of claim 11 , wherein the starting steviol glycoside substrate comprises stevioside, rebaudioside A, or any combination thereof and the produced steviol glycoside is rebaudioside M.

19. The method of claim 12 , wherein the starting steviol glycoside substrate is rebaudioside KA and the produced steviol glycoside is rebaudioside E.

20. The method of claim 12 , wherein the starting steviol glycoside substrate is rubusoside and the produced steviol glycoside is rebaudioside KA.

21. The method of claim 12 , wherein the starting steviol glycoside substrate is rubusoside and the produced steviol glycoside is rebaudioside E.

22. The method of claim 7 , wherein the starting steviol glycoside substrate is selected from the group consisting of rubusoside, rebaudioside KA, stevioside, rebaudioside A, rebaudioside D, rebaudioside E, and any combination thereof.

23. The method of claim 7 for producing a steviol glycoside selected from the group consisting of rebaudioside KA, rebaudioside A, rebaudioside D, rebaudioside E, rebaudioside M, and any combination thereof by glycosylating a starting steviol glycoside substrate selected from the group consisting of rubusoside, rebaudioside KA, stevioside, rebaudioside A, rebaudioside D, rebaudioside E, and any combination thereof.

24. The method of claim 7 , further comprising separating said desired steviol glycoside from the culture medium.

25. The whole-cell catalyst composition of claim 1 , wherein the Pichia pastoris host cell is transformed to include more than one copy of each of said first and second nucleotide sequences.

Assignees

• Conagen Inc

Inventors

• Mao Guohong
• Vick Jacob Edward
• Li shi-yan
• Yu Xiaodan

Classifications

• C12N15/52

  Genes encoding for enzymes or proenzymes · CPC title

• C12P19/56 Primary

  having an oxygen atom of the saccharide radical directly bound to a condensed ring system having three or more carbocyclic rings, e.g. daunomycin, adriamycin · CPC title

• C12N9/1048 Primary

  Glycosyltransferases (2.4) · CPC title

• A23L27/36

  Terpene glycosides · CPC title

• A23V2002/00

  Food compositions, function of food ingredients or processes for food or foodstuffs · CPC title