IP Library Granted Patent US 12,735,685
Granted Patent B2
US 12,735,685 · App. 17/925,168 · Granted Sep 15, 2026

Enzymatic production of allulose

Inventor: Daniel Joseph Wichelecki (Charlottesville, VA)
Assignee: BONUMOSE, INC.
C12N9/1229C12N9/1051C12N9/90C12N9/92C12P19/24C12Y204/01001C12Y204/01018C12Y501/03C12Y503/01009C12Y504/02002
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,735,685
App. No.
17/925,168
Granted
Sep 15, 2026
Kind
B2
Abstract

The invention relates to improved processes for the enzymatic production of allulose using enzymes which have been characterized as having improved expression, improved stability, and low allulose to fructose conversion activity, relative to enzymes in other allulose production methods. Improved processes include steps of converting fructose-6-phosphate to allulose 6-phopsphate A6P) using an allulose 6-phosphate epimerase, and converting A6P to allulose using an allulose-6-phosphate phosphatase.

Claims (40)

1 . An improved process for the production of allulose from a saccharide, the improved process comprising the steps of:

converting fructose-6-phosphate (F6P) to allulose 6-phopsphate (A6P) using an allulose 6-phosphate epimerase (A6PE), wherein the A6PE comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 1; and

converting A6P to allulose using an allulose 6-phosphate phosphatase (A6PP), wherein the improved process produces more allulose than a process for producing allulose under the same process conditions using Bacillus thermoamylovorans A6PE comprising the amino acid sequence as set forth in SEQ ID NO: 4.

2 . An improved process for the production of allulose from a saccharide, the improved process comprising the steps of:

converting fructose-6-phosphate (F6P) to allulose 6-phopsphate (A6P) using an allulose 6-phosphate epimerase (A6PE); and

converting A6P to allulose using an allulose-6-phoshpate phosphatase (A6PP), wherein the A6PP comprises the amino acid sequence as set forth in SEQ ID NO: 2,

wherein the improved process produces more allulose than a process for producing allulose under the same process conditions using Clostridium thermocellum A6PP comprising the amino acid sequence as set forth in SEQ ID NO: 10.

3 . The process of any one of claim 2 , further comprising a step of converting glucose 6-phosphate (G6P) to the F6P, wherein the step is catalyzed by a phosphoglucoisomerase (PGI).

4 . The process of claim 3 , further comprising a step of converting glucose 1-phosphate (G1P) to the G6P, wherein the step is catalyzed by a phosphoglucomutase (PGM).

5 . The process of claim 4 , further comprising a step of converting a saccharide to the G1P, wherein the step is catalyzed by at least one enzyme, wherein the saccharide is selected from the group consisting of a starch or derivative thereof, cellulose or a derivative thereof and sucrose.

6 . The process of claim 5 , wherein the at least one enzyme is selected from the group consisting of alpha-glucan phosphorylase (αGP), maltose phosphorylase, sucrose phosphorylase, cellodextrin phosphorylase, cellobiose phosphorylase, and cellulose phosphorylase.

7 . The process of claim 5 , wherein the saccharide is starch or a derivative thereof selected from the group consisting of amylose, amylopectin, soluble starch, amylodextrin, maltodextrin, maltose, maltotriose, and glucose.

8 . The process of claim 7 , further comprising a step of converting starch to a starch derivative wherein the starch derivative is prepared by enzymatic hydrolysis of starch or by acid hydrolysis of starch.

9 . The process of claim 8 , wherein a 4-glucan transferase (4GT) is added to the process.

10 . The process of claim 8 , wherein the starch derivative is prepared by enzymatic hydrolysis of starch catalyzed by an isoamylase, a pullulanase, an alpha-amylase, or a combination thereof.

11 . The process of claim 2 , further comprising:

a step of converting fructose to F6P catalyzed by at least one enzyme; and

optionally, a step of converting sucrose to fructose catalyzed by at least one enzyme.

12 . The process of claim 3 , further comprising:

a step of converting glucose to G6P catalyzed by at least one enzyme, and

optionally, a step of converting sucrose to glucose catalyzed by at least one enzyme.

13 . The process of claim 2 , further comprising the steps of:

(i) converting a saccharide to glucose 1-phosphate (G1P) using an α-glucan phosphorylase or starch phosphorylase, wherein the saccharide is selected from the group consisting of starch, one or more derivatives of starch, or a combination thereof;

(ii) converting G1P to glucose 6-phosphate (G6P) using a phosphoglucomutase (PGM); and

(iii) converting G6P to fructose 6-phosphate (F6P) using a phosphoglucoisomerase (PGI); wherein all process steps are conducted together in a single reaction vessel.

14 . The process of claim 2 , wherein the process steps are conducted under at least one of the following process conditions:

(a) at a temperature ranging from about 37° C. to about 85° C.;

(b) at a pH ranging from about 5.0 to about 9.0; or

(c) for about 1 hour to about 48 hours.

15 . The process of claim 13 , wherein the process steps are conducted under at least one of the following process conditions:

(a) without adenosine triphosphate (ATP) as a source of phosphate;

(b) without nicotinamide adenosine dinucleotide;

(c) at a phosphate concentration from about 0.1 mM to about 150 mM;

(d) at a Mg 2+ concentration from about 0.1 mM to 50 mM;

(e) at a Co 2+ concentration from about 0.1 mM to 50 mM; and

(f) wherein phosphate is recycled.

16 . The process of claim 15 , wherein phosphate is recycled, and wherein phosphate ions produced by A6PP dephosphorylation of A6P are used in the process step of converting a saccharide to G1P.

17 . The process of any one of claim 13 , further comprising the step of separating recovering the allulose produced, wherein the separation recovery is not via chromatography separation.

18 . The process of claim 2 further comprising a step of adding the allulose to a consumable product.

19 . The improved process of claim 1 , wherein the A6PP comprises an amino acid sequence having at least 90% sequence identity to SEQ ID NO: 2.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2023
From: WICHELECKI, DANIEL JOSEPH
To: BONUMOSE INC.
Reel/Frame 062348/0068 →
Continuity (2)
Provisional Application 63026294 · May 18, 2020
Related Publication 20230183768A1 · Jun 15, 2023
References Cited (17)
US 10704069B2 · Wichelecki · 2020 [cited by examiner]
US 11053528B2 · Wichelecki · 2021 [cited by examiner]
US 11078506B2 · Wichelecki · 2021 [cited by examiner]
US 11168342B2 · Wichelecki · 2021 [cited by examiner]
TW 201943854A · 2019 [cited by applicant]
WO 2018112139A1 · 2018 [cited by applicant]
WO 2018129275A1 · 2018 [cited by applicant]
WO 2018169957A1 · 2018 [cited by applicant]
WO 2020235830A1 · 2020 [cited by applicant]
WO 2021011881A1 · 2021 [cited by applicant]
A0A0E3NCH4_METTE. UniProtKB/TrEMBL Database. Apr. 10, 2019. [cited by examiner]
Fransceus. J Ind Microbiol Biotechnol. May 2017;44(4-5):687-695. [cited by examiner]
Sanavia. Computational and Structural Biotechnology Journal, vol. 18, 2020, pp. 1968-1979. [cited by examiner]
Studer (Residue mutations and their impact on protein structure and function: detecting beneficial and pathogenic changes. Biochem. J. (2013) 449, 581-594. [cited by examiner]
A0A223HZI7. UniProtKB/TrEMBL. Dec. 20, 2017. [cited by examiner]
International Search Report and Written Opinion in International Application No. PCT/US2021/032952, dated Nov. 17, 2021. [cited by applicant]
UniProtKB submission A0A223HZI7, Allulose-6-phosphate 3-epimerase, Oct. 25, 2017. [cited by applicant]