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Detection of a glycosylated form of hen egg white lysozyme

Authors :
Jean Trudel
Alain Asselin
Source :
Biochemistry and Cell Biology. 73:307-309
Publication Year :
1995
Publisher :
Canadian Science Publishing, 1995.

Abstract

By assaying lysozyme activity after denaturing polyacrylamide gel electrophoresis of commercial hen egg white lysozyme preparations, minor lysozymal activity was detected as an 18-kDa protein. After electrophoretic purification for microsequencing, the N-terminus sequence of the 18-kDa lysozyme was found to be identical with mature 14.4-kDa hen egg white lysozyme. The 18-kDa hen egg white lysozyme was judged to be glycosylated based on a 3.6-kDa decrease in molecular mass after N-glycosidase F treatment, binding to concanavalin A – Sepharose, and staining with periodate – Schiff's reagent. The minor form corresponded to about 0.3% of lyzozyme molecules.Key words: lysozyme, glycosylation, sequential PAGE, N-terminus microsequencing.

Details

ISSN :
12086002 and 08298211
Volume :
73
Database :
OpenAIRE
Journal :
Biochemistry and Cell Biology
Accession number :
edsair.doi.dedup.....2aaea6443f46f3293852bf74510e86bf
Full Text :
https://doi.org/10.1139/o95-038