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      Generation of Arabidopsis thaliana plants with complex N-glycans lacking beta1,2-linked xylose and core alpha1,3-linked fucose.

      Febs Letters
      Acetylglucosamine, Arabidopsis, enzymology, genetics, Blotting, Western, Fucose, analysis, deficiency, Fucosyltransferases, Glycosylation, Mutation, Pentosyltransferases, Polysaccharides, biosynthesis, chemistry, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Xylose

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          Abstract

          The plant glycosyltransferases, beta1,2-xylosyltransferase (XylT) and core alpha1,3-fucosyltransferase (FucT), are responsible for the transfer of beta1,2-linked xylose and core alpha1,3-linked fucose residues to glycoprotein N-glycans. These glycan epitopes are not present in humans and thus may cause immunological responses, which represent a limitation for the therapeutic use of recombinant mammalian glycoproteins produced in transgenic plants. Here we report the genetic modification of the N-glycosylation pathway in Arabidopsis thaliana plants. Knockout plants were generated with complete deficiency of XylT and FucT. These plants lack antigenic protein-bound N-glycans and instead synthesise predominantly structures with two terminal betaN-acetylglucosamine residues (GlcNAc(2)Man(3)GlcNAc(2)).

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