Size distribution and general structural features of N‐linked oligosaccharides from the methylotrophic yeast, Pichia pastoris
- 1 March 1989
- Vol. 5 (2) , 107-115
- https://doi.org/10.1002/yea.320050206
Abstract
The secreted glycoproteins of Pichia pastoris contain more than 35% of their N‐linked oligosaccharides as structures smaller than Man14GlcNAc2 (Man = mannose; GlcNAc = N‐acetylglucosamine). On heterologous invertase produced in P. pastoris, approximately 85% of the oligosaccharides are in the size range Man8–14GlcNAc2. The structures appear to contain α‐linked mannose. In addition, one‐third of the structures contain net negative charge and can be radio‐labelled in vivo with 32P. The largest oligosaccharides isolated from P. pastoris are significantly shorter than the hypermannosylated structures typical of S. cerevisiae, indicating that the factors which influence the processing of N‐linked oligosaccharides in P. pastoris are different from those which influence processing in S. cerevisiae. The smaller N‐linked oligosaccharides synthesized by P. pastoris resemble high‐mannose oligosaccharides synthesized by animal cells, and this finding increases the utility of P. pastoris as a host for the production of heterologous glycoproteins.Keywords
This publication has 18 references indexed in Scilit:
- Characterization of the glycosylation sites in yeast external invertase. I. N-linked oligosaccharide content of the individual sequons.Journal of Biological Chemistry, 1988
- High-Level Secretion of Glycosylated Invertase in the Methylotrophic Yeast, Pichia PastorisNature Biotechnology, 1987
- High–Level Expression and Efficient Assembly of Hepatitis B Surface Antigen in the Methylotrophic Yeast, Pichia PastorisNature Biotechnology, 1987
- Expression of thelacZgene from two methanol-regulated promoters inPichia pastorisNucleic Acids Research, 1987
- Pichia pastoris as a host system for transformations.Molecular and Cellular Biology, 1985
- Retention of membrane proteins by the endoplasmic reticulum.The Journal of cell biology, 1985
- An MF alpha 1-SUC2 (alpha-factor-invertase) gene fusion for study of protein localization and gene expression in yeast.Proceedings of the National Academy of Sciences, 1983
- Early stages in the yeast secretory pathway are required for transport of carboxypeptidase Y to the vacuoleCell, 1982
- Two differentially regulated mRNAs with different 5′ ends encode secreted and intracellular forms of yeast invertaseCell, 1982
- Subunit structure of external invertase from Saccharomyces cerevisiae.Journal of Biological Chemistry, 1977