Assaying Fucosidase Activity.
Cation dependence
Enzymatic activity
Fucosidase
HPAEC-PAD
Reaction rate
Substrate specificity
pH optimum
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
14
3
2019
pubmed:
14
3
2019
medline:
23
7
2019
Statut:
ppublish
Résumé
The characterization of a recombinant glycosidase can be done with commercially available substrates, which enable testing of enzyme functionality and determination of linkage specificity. Colorimetric assays with p-nitrophenyl substrates provide a relatively simple and fast way of screening conditions which could affect enzyme activity (buffer, pH, ion dependence, temperature). These substrates are useful for the determination of activity optima and the characterization of basic activity parameters. However, testing for linkage specificity should be performed on more complex sugars presenting a range of different glycosidic bonds and might need more sophisticated methods of analysis. This protocol provides comprehensive instructions on how to perform an initial characterization of your glycosidase using a recombinant α-L-fucosidase as an example.
Identifiants
pubmed: 30864139
doi: 10.1007/978-1-4939-9154-9_21
doi:
Substances chimiques
Nitrophenols
0
Recombinant Proteins
0
4-nitrophenyl
2395-99-5
alpha-L-Fucosidase
EC 3.2.1.51
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
269-278Subventions
Organisme : Austrian Science Fund FWF
ID : W 1224
Pays : Austria