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Detection of a glycosylated form of hen egg white lysozyme
- 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