Abstract
To examine the role of the connecting region in the artificial bifunctional enzyme beta-galactosidase/galactose dehydrogenase, linkers of different length were inserted between the catalytic units. The specific activity of the galactose dehydrogenase part of the complex was increased when longer linkers (9 and 13 amino acids) were used as connectors. These bifunctional enzymes were predominantly found to comprise hexamers, however, complexes of higher molecular weight were also formed. The sequential reaction was carried out more efficiently when hybrid enzymes with the longer linkers were used as demonstrated both in vitro by using purified protein preparations as well as in vivo by determining the growth rates of recombinant E. coli cells on a minimal medium containing lactose.
Original language | English |
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Pages (from-to) | 154-60 |
Number of pages | 7 |
Journal | Biochimica et Biophysica Acta |
Volume | 1293 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1996 Mar 7 |
Subject classification (UKÄ)
- Biochemistry and Molecular Biology
Free keywords
- Amino Acid Sequence
- Base Sequence
- Chromatography, Gel
- Cloning, Molecular
- Enzyme Stability
- Escherichia coli
- Galactose
- Galactose Dehydrogenases
- Hydrogen-Ion Concentration
- Kinetics
- Lactose
- Molecular Sequence Data
- Molecular Weight
- Multienzyme Complexes
- NAD
- Peptides
- Protein Conformation
- Recombinant Fusion Proteins
- Temperature
- beta-Galactosidase