IP Library Granted Patent US 8,278,062
Granted Patent B2
US 8,278,062 · App. 12/400,268 · Granted Oct 2, 2012

Method of using lipid acyltransferase

Assignee: DuPont Nutrition Biosciences ApS
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Quick Facts
Patent No.
US 8,278,062
App. No.
12/400,268
Granted
Oct 2, 2012
Kind
B2
Abstract

A method of producing one or more of a carbohydrate ester, a protein ester, a protein subunit ester or a hydroxyl acid ester, which method comprises admixing an acyl donor, an acyl acceptor and water to produce a high water environment comprising 5-98% water, wherein said acyl donor is a lipid substrate selected from one or more of the group consisting of a phospholipid, a lysophospholipid, a triacylglyceride, a diglyceride, a glycolipid or a lysoglycolipid and said acyl acceptor is selected from one ore more of the group consisting of a carbohydrate, a protein, a protein subunit, or a hydroxyl acid; and contacting the admixture with a lipid acyltransferase, such that said lipid acyl transferase catalyses one or both of the following reactions: alcoholysis or transesterification.

Claims (13)

1. A method of producing a carbohydrate ester, a protein ester, a protein subunit ester or a hydroxy acid ester, wherein the method comprises contacting an acyl donor, an acyl acceptor and 5-98% water with a lipid acyltransferase enzyme capable of transferring an acyl group from a lipid to one or more of the following acyl acceptors: a sterol, a stanol, a carbohydrate, a protein or a sub-unit thereof, and glycerol, whereby the carbohydrate ester, the protein ester, the protein subunit ester or the hydroxy acid ester is produced; and wherein the lipid acyltransferase when tested using the Transferase Assay in Buffered Substrate has at least 5% acyltransferase activity (relative acyltransferase activity) wherein the Transferase Assay in Buffered Substrate comprises: (a) heating to 35° C. a substrate solution comprising phosphatidylcholine, cholesterol, water and HEPES buffer, wherein the substrate solution comprises approximately 95% water and has pH 7.0; (b) adding an enzyme to the substrate solution; and (c) determining acyltransferase activity of the enzyme based upon cholesterol ester and fatty acids formed.

2. The method of claim 1 , wherein the acyl donor is selected from a phospholipid, a lysophospholipid, a triacylglyceride, a diglyceride, a glycolipid or a lysoglycolipid.

3. The method of claim 1 , wherein the acyl acceptor is selected from a carbohydrate, a protein, a protein subunit, or a hydroxy acid.

4. The method according to claim 1 , wherein the lipid acyltransferase is capable of transferring an acyl group from a glycolipid and/or phospholipid to one of the following acceptor substrates: a carbohydrate, a protein, a protein subunit, or a hydroxy acid.

5. The method of claim 1 , wherein the acyl acceptor is a carbohydrate.

6. The method of claim 1 , wherein the acyl acceptor is a hydroxy acid.

7. A method according to claim 1 wherein the method further comprises purifying the carbohydrate ester, protein ester, protein subunit ester or hydroxy acid ester.

8. The method of claim 1 , wherein the enzyme is immobilized.

9. The method of claim 1 , wherein the enzyme additionally has glycolipase activity.

10. The method of claim 1 wherein the lipid acyltransferase is from an organism from one or more of the following genera: Aeromonas, Streptomyces, Saccharomyces, Lactococcus, Mycobacterium, Streptococcus, Lactobacillus, Desulfitobacterium, Bacillus, Campylobacter, Vibrionaceae, Xylella, Sulfolobus, Aspergillus, Schizosaccharomyces, Listeria, Neisseria, Mesorhizobium, Ralstonia, Xanthomonas and Candida.

11. The method of claim 1 wherein the lipid acyltransferase comprises amino acid sequence motif GDSX, wherein X is one or more of the following amino acid residues L, A, V, I, F, Y, H, Q, T, N, M or S.

12. A method of producing a protein ester, a protein subunit ester or a hydroxy acid ester comprising:

admixing an acyl donor, an acyl acceptor and water to form an admixture wherein the acyl donor and acyl acceptor are in an environment comprising 5-98% water, and contacting the admixture with a lipid acyltransferase, wherein: the acyl donor is a lipid substrate selected from one or more of the group consisting of a phospholipid, a lysophospholipid, a triacylglyceride, a diglyceride, a glycolipid or a lysoglycolipid; the acyl acceptor is a protein, a protein subunit or a hydroxy acid; the lipid acyltransferase possesses acyl transferase activity and catalyses one or both of the following reactions: alcoholysis or transesterification; and the lipid acyltransferase has an amino acid sequence containing a GDSX motif, wherein X is one or more of the following amino acid residues L, A, V, I, F, Y, H, Q, T, N, M or S, and the lipid acyltransferase amino acid sequence is expressed by a nucleic acid molecule having at least 90% sequence identity with SEQ ID NO: 8.

Assignments (2)
CHANGE OF NAME Recorded May 31, 2012
From: DANISCO A/S
To: DUPONT NUTRITION BIOSCIENCES APS
Reel/Frame 028306/0882 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2010
From: DEKREIJ, ARNO; MADRID, SUSAN MAMPUSTI; MIKKELSEN, JORN DALGAARD; SOE, JORN BORCH
To: DANISCO A/S
Reel/Frame 025171/0313 →
Priority Claims (7)
GB 0301117.8 · Jan 14, 2003 · national
GB 0301118.6 · Jan 17, 2003 · national
GB 0301119.4 · Jan 17, 2003 · national
GB 0301120.2 · Jan 17, 2003 · national
GB 0301121.0 · Jan 17, 2003 · national
GB 0301122.8 · Jan 17, 2003 · national
GB 0330016.7 · Dec 24, 2003 · national
Continuity (4)
Division 11182480 · Jul 15, 2005
Continuation In Part PCTIB2004000575 · Jan 15, 2004
Provisional Application 60489441 · Jul 23, 2003
Related Publication 20100285525A1 · Nov 11, 2010