Pyruvate carboxylase from Corynebacterium glutamicum : purification and characterization.
Anaplerotic reactions
Corynebacterium glutamicum
Enzyme assay
Enzyme kinetics
Enzyme purification
Inhibitors
Kinetic parameters
Pyruvate carboxylase
Journal
Applied microbiology and biotechnology
ISSN: 1432-0614
Titre abrégé: Appl Microbiol Biotechnol
Pays: Germany
ID NLM: 8406612
Informations de publication
Date de publication:
Aug 2019
Aug 2019
Historique:
received:
21
03
2019
accepted:
11
06
2019
revised:
10
06
2019
pubmed:
27
6
2019
medline:
31
12
2019
entrez:
27
6
2019
Statut:
ppublish
Résumé
Pyruvate carboxylase of Corynebacterium glutamicum serves as anaplerotic enzyme when cells are growing on carbohydrates and plays an important role in the industrial production of metabolites derived from the tricarboxylic acid cycle, such as L-glutamate or L-lysine. Previous studies suggested that the enzyme from C. glutamicum is very labile, as activity could only be measured in permeabilized cells, but not in cell-free extracts. In this study, we established conditions allowing activity measurements in cell-free extracts of C. glutamicum and purification of the enzyme by avidin affinity chromatography and gel filtration. Using a coupled enzymatic assay with malate dehydrogenase, V
Identifiants
pubmed: 31240367
doi: 10.1007/s00253-019-09982-x
pii: 10.1007/s00253-019-09982-x
doi:
Substances chimiques
Enzyme Inhibitors
0
Pyruvic Acid
8558G7RUTR
Adenosine Triphosphate
8L70Q75FXE
Pyruvate Carboxylase
EC 6.4.1.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM