Fucosyltransferases and their use in producing fucosylated oligosaccharides

1. A method for producing a fucosylated oligosaccharide, the method comprising:

a) providing at least one genetically engineered cell that has been engineered to express a heterologous fucosyltransferase, wherein the heterologous fucosyltransferase comprises an amino acid sequence having at least 80% sequence identity to one of SEQ ID NOs: 17-26 and 28-30, wherein the fucosyltransferase is capable of transferring a fucose residue from a donor substrate to an acceptor molecule;

b) cultivating by fermentation the at least one genetically engineered cell in the presence of at least one carbon source, an acceptor molecule being a lactotetraose, and a donor substrate, comprising a fucose residue, and under conditions suitable for the at least one genetically engineered cell to transfer the fucose residue from the donor substrate to the acceptor molecule to produce the fucosylated oligosaccharide.

2. The method according to claim 1 , wherein the acceptor molecule is selected from the group consisting of Lacto-N-tetraose (LNT) and Lacto-N-neotetraose (LNnT).

3. The method according to claim 2 , wherein the acceptor is LNT and the heterologous fucosyltransferase is selected from the group consisting of SEQ ID NOs: 18-22, 24, 25, 28 and 30, functional variants of the polypeptides of SEQ ID NOs: 18-22, 24, 25, 28 and 30 having at least 80% sequence identity to SEQ ID NOs: 18-22, 24, 25, 28, and 30.

4. The method according to claim 2 , wherein the acceptor is LNnT and the heterologous fucosyltransferase is selected from the group consisting of SEQ ID NOs: 17, 20, 26, 28, and 30, and functional variants of the polypeptides of SEQ ID NOs: 17, 20, 26, 28 and 30 having at least 80% sequence identity to SEQ ID NOs: 17, 20, 26, 28, and 30.

5. The method according to claim 2 , wherein the fucosyltransferase is encoded by a gene with a sequence selected from the group consisting of SEQ ID NOs: 5, 11, and 14.

6. The method according to claim 5 , wherein the gene has the sequence of SEQ ID NO: 14.

7. The method according to claim 2 , wherein the acceptor molecule is LNT and the fucosyltransferase is encoded by a gene having a sequence selected from the group consisting of SEQ ID NOs: 3-7, 9-11, and 14.

8. The method according to claim 2 , wherein the acceptor molecule is LNnT and the fucosyltransferase is encoded by a gene having a sequence selected from the group consisting of SEQ ID NOs: 2, 5, 11, 12, and 14.

9. The method according to claim 1 , wherein the heterologous fucosyltransferase is encoded by a nucleic acid molecule, wherein the nucleic acid molecule:

i) comprises a nucleotide sequence set forth in any one of SEQ ID NOs: 2-12 and 14-15.

ii) comprises a nucleotide sequence having a sequence identity of at least 80% to any one of SEQ ID NOs: 2-12 and 14-15 over the entire length of the sequence;

iii) comprises a nucleotide sequence which encodes a polypeptide having an amino acid sequence selected from any one of SEQ ID NOs: 17-26 and 28-30; or

iv) comprises a nucleotide sequence which encodes a polypeptide having at least 80% sequence identity to any one of SEQ ID NOs: 17-26 and 28-30.

10. The method according to claim 9 , wherein said genetically engineered cell is Escherichia coli and the nucleic acid molecule comprises a nucleotide sequence which encodes a polypeptide having at least 80% sequence identity to any one of SEQ ID NOs: 17-26, 28, and 30 that is codon-optimized for expression in Escherichia coli except if the nucleic acid molecule encodes the amino acid sequence of SEQ ID NO: 29.

11. The method according to claim 1 , wherein said at least one genetically engineered cell is Escherichia coli.

12. The method according to claim 1 , wherein the method further comprises recovering the fucosylated oligosaccharide.