US2011300584A1PendingUtilityA1

Synthesis of fucosylated compounds

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Assignee: HUEFNER ERICPriority: Dec 19, 2008Filed: Dec 18, 2009Published: Dec 8, 2011
Est. expiryDec 19, 2028(~2.4 yrs left)· nominal 20-yr term from priority
A23L 33/00C12N 9/1051C12N 9/12A23V 2002/00
72
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Claims

Abstract

A method for making a genetically modified cell having the ability to produce fucosylated compounds comprising the steps of transforming the cell to express a fucose kinase transforming the cell to express a fucose-1-phosphate guanylyltransferase transforming the cell to express a fucosyltransferase.

Claims

exact text as granted — not AI-modified
1 . A method for making a genetically modified cell having the ability to produce fucosylated compounds comprising the steps of
 transforming the cell to express a fucose kinase   transforming the cell to express a fucose-1-phosphate guanylyltransferase   transforming the cell to express a fucosyltransferase.   
     
     
         2 . The method of  claim 1 , wherein the genetically modified cell is a microorganismm selected from the group consisting of the genera  Escherichia, Klebsiella, Helicobacter, Bacillus, Lactobacillus, Streptococcus, Lactococcus, Pichia, Saccharomyces  and  Kluyveromyces.    
     
     
         3 . The method of  claim 1 , wherein the fucose kinase and the fucose-1-phosphate guanylyltransferase are combined in a bifunctional enzyme. 
     
     
         4 . The method of  claim 3 , wherein the bifunctional fucose kinase/fucose-1-phosphate guanylyltransferase is selected of bifunctional fucose kinase/fucose-1-phosphate guanylyltransferase dervied from the group consisting of the genera  Bacteroides, Lentisphaera, Ruminococcus, Solibacter, Arabidopsis, Oryza, Physcomitrella, Vitis, Danio, Bos, Equus, Macaca, Pan, Homo, Rattus, Mus  and  Xenopus.    
     
     
         5 . The method of  claim 1 , wherein the fucosyltransferase is derived from an organism selected from the group consisting of the genera  Helicobacter, Escherichia, Yersinia, Enterococcus, Shigella, Klebsiella, Salmonella, Bacteroides, Dictyosetelium, Arabidopsis, Drosophila, Homo, Bos, Mus, Rattus, Gallus, Canis  and  Sus.    
     
     
         6 . The method of  claim 1 , wherein a catabolic pathway of said cell for fucose is inactivated. 
     
     
         7 . The method of  claim 6 , wherein the catabolic pathway for fucose is inactivated by inactivating one or several genes selected from the group consisting of a fucose-1-phosphate aldolase gene, a fucose isomerase gene and a fuculose kinase gene. 
     
     
         8 . The method of  claim 1 , wherein the fucosylated compound is a fucosyllactose, preferably 2′-fucosyllactose, 3-fucosyllactose or lactodifucotetraose. 
     
     
         9 . A genetically modified cell obtainable by the method of  claim 1 . 
     
     
         10 . A method for making fucosylated compound comprising the steps of cultivating the cell of  claim 9  under suitable cultivation conditions in a medium comprising fucose and an acceptor substrate. 
     
     
         11 . The method of  claim 10 , wherein the acceptor substrate is a mono-, di- or oligosaccharide or a peptide. 
     
     
         12 . The method of  claim 10 , wherein the acceptor substrate is lactose, 2′-fucosyllactose or 3-fucosyllactose. 
     
     
         13 . The method of  claim 10 , wherein the fucosylated compound is a fucosyllactose, preferably 2′-fucosyllactose or 3-fucosyllactose, or lactodifucotetraose.

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