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- W2724329636 endingPage "141" @default.
- W2724329636 startingPage "133" @default.
- W2724329636 abstract "Glycosylation is an important protein modification in all eukaryotes. Whereas the early asparagine-linked glycosylation (N-glycosylation) and N-glycan processing steps in the endoplasmic reticulum are conserved between mammals and plants, the maturation of complex N-glycans in the Golgi apparatus differs considerably. Due to a restricted number of Golgi-resident N-glycan processing enzymes and the absence of nucleotide sugars such as CMP-N-acetylneuraminic acid, plants produce only a limited repertoire of different N-glycan structures. Moreover, mammalian mucin-type O-glycosylation of serine or threonine residues has not been described in plants and the required machinery is not encoded in their genome which enables de novo build-up of the pathway. As a consequence, plants are very well-suited for the production of homogenous N- and O-glycans and are increasingly used for the production of recombinant glycoproteins with custom-made glycans that may result in the generation of biopharmaceuticals with improved therapeutic potential." @default.
- W2724329636 created "2017-07-14" @default.
- W2724329636 creator A5010190025 @default.
- W2724329636 creator A5018118317 @default.
- W2724329636 date "2018-08-01" @default.
- W2724329636 modified "2023-10-14" @default.
- W2724329636 title "Plant glyco-biotechnology" @default.
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