scispace - formally typeset
Open AccessJournal ArticleDOI

Mutations in the DNA gyrB gene that are temperature sensitive for lambda site-specific recombination, Mu growth, and plasmid maintenance.

TLDR
These two mutations in the gyrB gene of Escherichia coli K12 obtained from an initial selection for resistance to coumermycin A1 and a subsequent screening for bacteria that fail to support site-specific recombination of phage lambda have a temperature-sensitive Him- phenotype, supporting site- specific recombination efficiently at low temperature, but inefficiently at high temperatures.
Abstract
We report the isolation of two mutations in the gyrB gene of Escherichia coli K12 obtained from an initial selection for resistance to coumermycin A1 and a subsequent screening for bacteria that fail to support site-specific recombination of phage lambda, i.e., Him-. These two mutations have a temperature-sensitive Him- phenotype, supporting site-specific recombination efficiently at low temperature, but inefficiently at high temperatures. Like other Him mutants, the gyrB-him mutants fail to plate phage Mu; again this defect is observed only at high temperatures. Additional thermally sensitive characteristics have also been observed; growth of lambda as well as maintenance of the plasmids pBR322 and F' gal are reduced at high temperature. Restriction of foreign DNA imposed by a P1 prophage is also reduced in these mutants. The temperature-sensitive phenotypic characteristics imposed by both the gyrB-him-230(Ts) and gyrB-him-231(Ts) mutations correlate with in vitro studies that show decreased gyrase activity, especially at higher temperatures, and in vivo studies showing reduced supercoiling of lambda DNA in the mutants at high temperature.

read more

Citations
More filters
Journal ArticleDOI

Control of bacterial DNA supercoiling

TL;DR: Two DNA topoisomerases control the level of negative supercoiling in bacterial cells and the ratio of [ATP] to [ADP], to which gyrase is sensitive, may be involved in the response ofsupercoiling to growth conditions.
Journal ArticleDOI

Biology of bacterial deoxyribonucleic acid topoisomerases.

TL;DR: This work states that generalized Recombination, followed by Gyrase-Mediated Illegitimate Recombinations, and then Topoisomerases, Recombination, and RePAIR are viable strategies for DNA replication.
Journal ArticleDOI

Mutations in a new chromosomal gene of Escherichia coli K-12, pcnB, reduce plasmid copy number of pBR322 and its derivatives.

TL;DR: The pcnB mutant strain of Escherichia coli should be useful for cloning genes into pBR322 that have aberrant or deleterious effects on the cell when present in high copy number.
Journal ArticleDOI

Genetic and biochemical characterization of norfloxacin resistance in Escherichia coli.

TL;DR: In Escherichia coli the frequency of spontaneous single-step mutation to high levels of resistance to the newer 4-quinolone agent norfloxacin was confirmed to be over 300-fold lower than that to the older agent nalidixic acid.
References
More filters
Book

Experiments in molecular genetics

TL;DR: Molecular Genetics (Biology): An Overview | Sciencing Experimental in Molecular Genetics Experiments in molecular genetics (1972 edition) | Open ...
Journal ArticleDOI

A rapid alkaline extraction procedure for screening recombinant plasmid DNA

H C Birnboim, +1 more
TL;DR: In this paper, a procedure for extracting plasmid DNA from bacterial cells is described, which is simple enough to permit the analysis by gel electrophoresis of 100 or more clones per day, yet yields DNA which is pure enough to be digestible by restriction enzymes.

Arapid alkaline extraction procedure forscreening recombinant plasmid DNA

TL;DR: The method is simple enough to permit the analysis by gel electrophoresis of 100 or more clones per day yet yields plasmid DNA which is pure enough to be digestible by restriction enzymes, and achievesequate pH control without using a pH meter.
Journal ArticleDOI

Nonchromosomal Antibiotic Resistance in Bacteria: Genetic Transformation of Escherichia coli by R-Factor DNA

TL;DR: Covalently-closed, catenated, and open (nicked) circular forms of R-factor DNA are all effective in transformation, but denaturation and sonication abolish the transforming ability of R.factor DNA in this system.
Journal ArticleDOI

Transduction of linked genetic characters of the host by bacteriophage P1

TL;DR: Transduction of characters between bacteria of the coli and dysentery groups indicates genetic homologies between these groups.
Related Papers (5)