The 24 kDa N‐terminal sub‐domain of the DNA gyrase B protein binds coumarin drugs
- 1 May 1994
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 12 (3), 365-373
- https://doi.org/10.1111/j.1365-2958.1994.tb01026.x
Abstract
A number of lines of evidence suggest that the N‐terminal sub‐domain of the DNA gyrase B protein contains the binding site for the coumarin antibiotics. We have engineered a clone which encodes a 24 kDa protein which represents this domain. Bacteria which overproduce this protein show an elevated level of resistance to coumarins, suggestive of binding of the 24 kDa protein to the drugs In vivo. In vitro we find that the 24 kDa protein does not interact with the gyrase A or B proteins or with DNA, and fails to hydrolyse ATP or show significant binding to ATP, ADP or ADPNP. However, we show that the 24 kDa protein binds coumarin drugs as tightly as the Intact B protein. A number of experiments suggest that the Interaction of the coumarins with the protein is predominantly hydrophobic in nature.Keywords
This publication has 38 references indexed in Scilit:
- Expression and analysis of two gyrB genes from the novobiocin producer, Streptomyces sphaeroidesMolecular Microbiology, 1993
- The 43-kilodalton N-terminal fragment of the DNA gyrase B protein hydrolyzes ATP and binds coumarin drugsBiochemistry, 1993
- gyrB mutations which confer coumarin resistance also affect DNA supercoiling and ATP hydrolysis by Escherichia coli DNA gyraseMolecular Microbiology, 1992
- Crystal structure of an N-terminal fragment of the DNA gyrase B proteinNature, 1991
- Preliminary crystallographic analysis of the ATP-hydrolysing domain of the Escherichia coli DNA gyrase B proteinJournal of Molecular Biology, 1991
- DNA Gyrase: Structure and FunctionCritical Reviews in Biochemistry and Molecular Biology, 1991
- Structure-activity relationships in DNA gyrase inhibitorsPharmacology & Therapeutics, 1990
- Clinical utility of DNA gyrase inhibitorsPharmacology & Therapeutics, 1989
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976