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Role of Asp544 in subunit I for Na(+) pumping by Vitreoscilla cytochrome bo
- Source :
- Biochemical and biophysical research communications. 348(4)
- Publication Year :
- 2006
-
Abstract
- The conserved Glu540 in subunit I of Escherichia coli cytochrome bo (a H+ pump) is replaced by Asp544 in the Vitreoscilla enzyme (a Na+ pump). Site-directed mutagenesis of the Vitreoscilla cytochrome bo operon changed this Asp to Glu, and both wild type and mutant cyo’s were transformed into E. coli strain GV100, which lacks cytochrome bo. Compared to the wild type transformant the Asp544Glu transformant had decreased ability to pump Na+ as well as decreased stimulation in respiratory activity in the presence of Na+. Preliminary experiments indicated that this mutant also had increased ability to pump protons, suggesting that this single change may provide cation pumping specificity in this group of enzymes.
- Subjects :
- Cytochrome
Operon
Protein subunit
Mutant
Biophysics
Glutamic Acid
medicine.disease_cause
Biochemistry
Bacterial Proteins
Multienzyme Complexes
medicine
NADH, NADPH Oxidoreductases
Molecular Biology
Escherichia coli
Cation Transport Proteins
Fluorescent Dyes
Aspartic Acid
Ion Transport
biology
Aminoacridines
Spectrum Analysis
Mutagenesis
Sodium
Wild type
Cell Biology
biology.organism_classification
Cytochrome b Group
Molecular biology
Protein Subunits
Amino Acid Substitution
Vitreoscilla
biology.protein
Mutagenesis, Site-Directed
Protons
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 348
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Biochemical and biophysical research communications
- Accession number :
- edsair.doi.dedup.....8d117ff307efefd0b75a516f6c9f3f64