Superactive β-galactosidase inclusion bodies.
Cloning, Molecular
Enzyme Stability
Escherichia coli
/ enzymology
Escherichia coli Proteins
/ chemistry
Gene Expression
Genetic Vectors
/ chemistry
Hot Temperature
Hydrogen-Ion Concentration
Inclusion Bodies
/ chemistry
Kinetics
Lactose
/ chemistry
Protein Aggregates
Recombinant Proteins
/ chemistry
Solubility
Structure-Activity Relationship
beta-Galactosidase
/ chemistry
Catalytic activity
Inclusion bodies
Protein desorption process
β-Galactosidase
Journal
Colloids and surfaces. B, Biointerfaces
ISSN: 1873-4367
Titre abrégé: Colloids Surf B Biointerfaces
Pays: Netherlands
ID NLM: 9315133
Informations de publication
Date de publication:
01 Jan 2019
01 Jan 2019
Historique:
received:
19
07
2018
revised:
23
09
2018
accepted:
17
10
2018
pubmed:
2
11
2018
medline:
22
3
2019
entrez:
2
11
2018
Statut:
ppublish
Résumé
Bacterial inclusion bodies (IBs) were historically considered one of the major obstacles in protein production through recombinant DNA techniques and conceived as amorphous deposits formed by passive and rather unspecific structures of unfolded proteins aggregates. Subsequent studies demonstrated that IBs contained an important quantity of active protein. In this work, we proved that recombinant β-galactosidase inclusion bodies (IB
Identifiants
pubmed: 30384274
pii: S0927-7765(18)30746-X
doi: 10.1016/j.colsurfb.2018.10.049
pii:
doi:
Substances chimiques
Escherichia coli Proteins
0
Protein Aggregates
0
Recombinant Proteins
0
beta-Galactosidase
EC 3.2.1.23
Lactose
J2B2A4N98G
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
769-775Informations de copyright
Copyright © 2018 Elsevier B.V. All rights reserved.