Abstract
DNA gyrase from Bacillus subtilis 168 was purified by affinity chromatography on novobiocin-Sepharose and shown to consist of two subunits, A and B, with molecular weights of 100,000 and 85,000, respectively. The B subunits, which contains novobiocin-sensitive. ATPase activity, could complement the gyrA protein of Escherichia coli. No complementation was detected between the A subunit and the E. coli gyrB protein.
MeSH Terms
Bacillus subtilis/enzymology,genetics
DNA Topoisomerases, Type II/isolation & purification,metabolism
DNA, Superhelical
Genetic Complementation Test
Kinetics
Macromolecular Substances
Molecular Weight
Chemicals
DNA, Superhelical
Macromolecular Substances
DNA Topoisomerases, Type II
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Orr E
Staudenbauer W L
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12 references, click to expand
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