Hexuronate C4-epimerase variant having improved D-tagatose conversion activity, and D-tagatose production method using same

Patent metadata

Field	Value
Publication number	US-10544439-B2
Application number	US-201715759511-A
Country	US
Kind code	B2
Filing date	Jul 31, 2017
Priority date	Jul 29, 2016
Publication date	Jan 28, 2020
Grant date	Jan 28, 2020

Abstract

Provided are a hexuronate C4-epimerase variant with improved activity in converting D-fructose by D-tagatose of hexuronate C4-epimerase and a method for production of D-tagatose using them.

First claim

The invention claimed is:

1. A hexuronate C4-epimerase variant comprising an amino acid sequence having at least 80% sequence identity to SEQ ID NO: 1, wherein said variant comprises a mutation at a position corresponding to tyrosine (Y)-403 amino acid residue of SEQ ID NO: 1.

2. The hexuronate C4-epimerase variant of claim 1 , wherein the tyrosine (Y)-403 amino acid residue is substituted with alanine (A), cysteine (C), aspartic acid (D), glutamic acid (E), phenylalanine (F), glycine (G), histidine (H), isoleucine (I), lysine (K), leucine (L), methionine (M), asparagine (N), proline (P), glutamine (Q), arginine (R), serine (S), threonine (T), valine (V) or tryptophan (W).

3. The hexuronate C4-epimerase variant of claim 1 , wherein in the hexuronate C4-epimerase variant, a serine (S)-125 amino acid residue from the N-terminal of the hexuronate C4-epimerase is additionally mutated.

4. The hexuronate C4-epimerase variant of claim 3 , wherein the serine (S)-125 amino acid residue is substituted with cysteine (C), tyrosine (Y), glutamine (Q), glutamic acid (E), threonine (T), asparagine (N), or aspartic acid (D).

5. The hexuronate C4-epimerase variant of claim 3 , wherein in the hexuronate C4-epimerase variant, (i) one to five amino acid residues selected from the group consisting of a serine (S)-185 amino acid residue, a valine (V)-267 amino acid residue, a serine (S)-268 amino acid residue, a threonine (T)-272 amino acid residue, a tryptophan (W)-306 amino acid residue, and an arginine (R)-386 amino acid residue, or (ii) a leucine (L)-77 amino acid residue, an alanine (A)-158 amino acid residue, or a combination of the amino acid residues from the N-terminal of the hexuronate C4-epimerase is additionally mutated.

6. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the serine (S)-268 amino acid residue is additionally mutated, and/or one or more amino acid residues selected from the group consisting of lysine (K)-164, aspartic acid (D)-168, glutamic acid (E)-175, asparagine (N)-297, and isoleucine (I)-388 from the N-terminal of the hexuronate C4-epimerase are additionally mutated.

7. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the valine (V)-267 amino acid residue and the arginine (R)-386 amino acid residue are additionally mutated, and/or proline (P)-351 from the N-terminal of the hexuronate C4-epimerase is additionally mutated.

8. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the serine (S)-185 amino acid residue, the valine (V)-267 amino acid residue, and the tryptophan (W)-306 amino acid residue are additionally mutated, and/or glutamic acid (E)-68 from the N-terminal of the hexuronate C4-epimerase is additionally mutated.

9. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the valine (V)-267 amino acid residue, the serine (S)-268 amino acid residue, and the arginine (R)-386 amino acid residue are additionally mutated, and/or one or more amino acid residues selected from the group consisting of glutamic acid (E)-60, methionine (M)-202, tyrosine (Y)-221, and tyrosine (Y)-242 from the N-terminal of the hexuronate C4-epimerase are additionally mutated.

10. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the serine (S)-185 amino acid residue, the valine (V)-267 amino acid residue, the serine (S)-268 amino acid residue, and the threonine (T)-272 amino acid residue are additionally mutated, and/or one or more amino acid residues selected from the group consisting of leucine (L)-91, aspartic acid (D)-141, and glycine (G)-176 from the N-terminal of the hexuronate C4-epimerase are additionally mutated.

11. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the valine (V)-267 amino acid residue, the serine (S)-268 amino acid residue, the threonine (T)-272 amino acid residue, and the tryptophan (W)-306 amino acid residue are additionally mutated, and/or one or more amino acid residues selected from the group consisting of valine (V)-284, and valine (V)-415 from the N-terminal of the hexuronate C4-epimerase are additionally mutated.

12. The hexuronate C4-epimerase variant of claim 5 , wherein in the hexuronate C4-epimerase variant in which the serine (S)-185 amino acid residue, the valine (V)-267 amino acid residue, the serine (S)-268 amino acid residue, the threonine (T)-272 amino acid residue, and the tryptophan (W)-306 amino acid residue are additionally mutated, and/or one or more amino acid residues selected from the group consisting of proline (P)-166, and aspartic acid (D)-231 from the N-terminal of the hexuronate C4-epimerase are additionally mutated.

13. The hexuronate C4-epimerase variant of claim 5 ,
wherein in the hexuronate C4-epimerase variant in which the serine (S)-185 amino acid residue, the valine (V)-267 amino acid residue, the serine (S)-268 amino acid residue, the threonine (T)-272 amino acid residue, and the tryptophan (W)-306 amino acid residue are additionally mutated, and/or valine (V)-126 from the N-terminal of the hexuronate C4-epimerase are additionally mutated.

14. A nucleic acid encoding the hexuronate C4-epimerase variant of claim 1 .

15. A method for producing D-tagatose comprising:
epimerizing D-fructose by contacting D-fructose with the hexuronate C4-epimerase variant according to claim 1 .

Assignees

• Cj Cheiljedang Corp

Inventors

• Yang Sung Jae
• Lee Young Mi
• Park Il Hyang
• Lee Chan-Hyoung
• Cho Hyun Kug
• Kim Seong Bo
• Kim Yang Hee
• Park Seung Won

Classifications

• C12P19/02

  Monosaccharides (2-ketogulonic acid C12P7/60) · CPC title

• C12P19/24 Primary

  produced by the action of an isomerase, e.g. fructose · CPC title

• C12N9/90 Primary

  Isomerases (5.) · CPC title

• C12Y501/02

  acting on hydroxy acids and derivatives (5.1.2) · CPC title

• C12Y501/03

  acting on carbohydrates and derivatives (5.1.3) · CPC title