IP Library Granted Patent US 7,326,770
Granted Patent B2
US 7,326,770 · App. 10/764,212 · Granted Feb 5, 2008

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Quick Facts
Patent No.
US 7,326,770
App. No.
10/764,212
Granted
Feb 5, 2008
Kind
B2
Abstract

This invention provides nucleic acid and amino acid sequences of fucosyltransferases from Helicobactor pylori . The invention also provides methods to use the fucosyltransferases to synthesize oligosaccharides, glycoproteins, and glycolipids.

Claims (29)

1. An isolated fucosyltransferase protein comprising a polypeptide that has greater than 90% identity to the full length of SEQ ID NO:16, wherein the fucosyltransferase catalyzes the transfer of a fucose residue from a donor substrate to an acceptor substrate.

2. The isolated fucosyltransferase of claim 1 , further comprising an amino acid tag.

3. The isolated fucosyltransferase of claim 1 , wherein the polypeptide is SEQ ID NO:16.

4. The isolated fucosyltransferase of claim 1 , wherein the fucosyltransferase catalyzes the transfer of fucose to an acceptor molecule selected from an N-acetylglucosamine residue and a glucose residue.

5. The isolated fucosyltransferase protein of claim 1 , wherein the polypeptide has greater than 95% identity to the full-length of SEQ ID NO:16.

6. A method for producing a fucosylated glycolipid, the method comprising:

contacting the isolated fucosyltransferase protein of claim 1 with a mixture comprising a donor substrate comprising a fucose residue, and an acceptor substrate on a glycolipid, under conditions where the fucosyltransferase catalyzes the transfer of the fucose residue from a donor substrate to the acceptor substrate on the glycolipid, thereby producing a fucosylated glycolipid.

7. A method of making a fucosylated oligosaccharide, the method comprising:

contacting the isolated fucosyltransferase of claim 1 with a mixture comprising a donor substrate comprising a fucose residue, and an acceptor substrate comprising a sugar or oligosaccharide, under conditions where the fusion protein catalyzes the transfer of a fucose residue from the donor substrate to the acceptor substrate, thereby producing a fucosylated oligosaccharide.

8. The method of claim 7 , wherein the method further comprises a step of purifying the fucosylated oligosaccharide.

9. The method of claim 7 , wherein a donor substrate is GDP-fucose.

10. The method of claim 7 , wherein the fucosyltransferase comprises an amino acid tag.

11. The method of claim 7 , wherein an acceptor substrate comprises a member selected from N-acetylglucosamine and glucose.

12. The method of claim 7 , wherein the acceptor substrate is Lacto-N-neo-Tetraose (LNnT).

13. The method of claim 12 , wherein the fucosylated oligosaccharide is Lacto-N-Fucopentaose III (LNFP III).

14. The method of claim 7 , wherein the mixture further comprises lactose, a β-1,3-N-acetylglucosaminyltransferase, and a β-1,4-galactosyltransferase.

15. The method of claim 14 , wherein the fucosylated oligosaccharide is Lacto-N-Fucopentaose III (LNFP III).

16. The method of claim 14 , wherein the β-1,3-N-acetylglucosaminyltransferase is a bacterial enzyme.

17. The method of claim 16 , wherein the β-1,3-N-acetylglucosaminyltransferase is from Neisseria gonococcus.

18. The method of claim 14 , wherein the β-1,4-galactosyltransferase is a bacterial enzyme.

19. The method of claim 18 , wherein the β-1,4-galactosyltransferase is from Neisseria gonococcus.

20. A method for producing a fucosylated glycoprotein, the method comprising:

contacting a host cell extract comprising a fucosyltransferase protein having greater than 90% identity to the full-length of SEQ ID NO:16, with a mixture comprising a donor substrate comprising a fucose residue, and an acceptor substrate on a glycoprotein, under conditions where the fucosyltransferase catalyzes the transfer of the fucose residue from a donor substrate to the acceptor substrate on the glycoprotein, thereby producing a fucosylated glycoprotein, wherein the host cell extract is heterologous to the fucosyltransferase protein.

21. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence having greater than 95% identity to the full-length of SEQ ID NO:16.

22. The method of claim 1 , wherein the polypeptide comprises SEQ ID NO:16.

23. The method of claim 1 , wherein the polypeptide further comprises an amino acid tag.

24. The method of claim 1 , wherein the method further comprises a step of purifying the fucosylated glycoprotein.

25. The method of claim 1 , wherein the acceptor substrate is selected from a glucose residue and an N-acetylglucosamine residue.

26. The method of claim 1 , wherein an acceptor substrate on the glycoprotein comprises Galb1-OR, Galb,3/4GlcNAc-OR, NeuAca2,3Galb1,3/4GlcNAc-Or, wherein R is an amino acid, a saccharide, an oligosaccharide, or an aglycon group having at least one carbon atom.

Assignments (5)
ADDRESS CHANGE Recorded Apr 22, 2014
From: BIOGENERIX AG
To: BIOGENERIX AG
Reel/Frame 032734/0829 →
MERGER Recorded Apr 22, 2014
From: BIOGENERIX GMBH
To: RATIOPHARM GMBH
Reel/Frame 032735/0296 →
CHANGE OF NAME Recorded Apr 22, 2014
From: BIOGENERIX AG
To: BIOGENERIX GMBH
Reel/Frame 032743/0923 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2009
From: NEOSE TECHNOLOGIES, INC.
To: BIOGENERIX, AG
Reel/Frame 022237/0030 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2004
From: SIMALA-GRANT, JOANNE; TAYLOR, DIANE; JOHNSON, KARL F.; BEZILA, DANIEL JAMES
To: NEOSE TECHNOLOGIES, INC.; GOVERNORS OF THE UNIVERSITY OF ALBERTA
Reel/Frame 014680/0652 →