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PMID: 1499571 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Distinct N-glycan fucosylation potentials of three lepidopteran cell lines.

European journal of biochemistry ·Vol. 207 ·No. 3 ·1992-08-01 ·Pages 987-93

Staudacher E, Kubelka V, März L

Abstract

The fucosyltransferase activities of three insect cell lines, MB-0503 (from Mamestra brassicae), BM-N (from Bombyx mori) and Sf-9 (from Spodoptera frugiperda), were investigated and compared with that of honeybee venom glands. Cell extracts and venom gland extracts were incubated with GDP-[14C]fucose and glycopeptides isolated from human IgG and from bovine fibrin. The labeled oligosaccharide products were released by peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase A, fluorescence marked with 2-aminopyridine and analyzed both by reversed-phase and size-fractionation HPLC. They were identified by their elution positions before and after exoglycosidase treatment in comparison with standard oligosaccharides. These experiments revealed distinct fucosylation potentials in the three cell lines tested. While MB-0503 cells, like honeybee venom glands, are able to transfer fucose into alpha 1-3 and alpha 1-6 linkage to the innermost N-acetylglucosamine, only alpha 1-6-fucosyl linkages were detected with BM-N and Sf-9 cells.

MeSH Terms
Animals Bee Venoms/chemistry Carbohydrate Sequence Cattle Cell Line Chromatography, High Pressure Liquid Fucosyltransferases/metabolism Humans Lepidoptera/cytology,metabolism Molecular Sequence Data Polysaccharides/metabolism Substrate Specificity
Chemicals
Bee Venoms Polysaccharides Fucosyltransferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Staudacher E
Institut für Chemie, Universität für Bodenkultur, Vienna, Austria.
Kubelka V
März L
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1992-08-01
Pages
987-93
Language
English
Region
England
NLM ID
0107600
Subset
IM
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