Difference between revisions of "PMID:7007354"

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(Table edited by Wameza via TableEdit)
(Table edited by Wameza via TableEdit)
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*Genotype of Reference Strain: ''dnaA<sup>+</sup>''
 
*Genotype of Reference Strain: ''dnaA<sup>+</sup>''
*Genotype of Experimental Strain : ''dnaA311''
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*Genotype of Experimental Strain : ''dnaA311(Am)''
 
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*Reference Condition:
 
*Reference Condition:
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*Genotype of Reference Strain: ''dnaA<sup>+</sup>''
 
*Genotype of Reference Strain: ''dnaA<sup>+</sup>''
*Genotype of Experimental Strain : ''dnaA366''
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*Genotype of Experimental Strain : ''dnaA366(Am)''
 
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*Reference Condition:
 
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*Genotype of Reference Strain: ''dnaA<sup>+</sup>''
 
*Genotype of Reference Strain: ''dnaA<sup>+</sup>''
*Genotype of Experimental Strain : ''dnaA367''
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*Genotype of Experimental Strain : ''dnaA367(Am)''
 
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*Reference Condition:
 
*Reference Condition:

Revision as of 17:03, 12 April 2013

Citation

Schaus, N, O'Day, K, Peters, W and Wright, A (1981) Isolation and characterization of amber mutations in gene dnaA of escherichia coli K-12. J. Bacteriol. 145:904-13

Abstract

Amber mutants with defects in the dnaA gene of Escherichia coli K-12 were isolated after localized mutagenesis of the tna-dnaA region of the chromosome. We isolated 36 mutants defective in the initiation of deoxyribonucleic acid replication as determined by their dependence upon integrative suppression by a P2 sig5 prophage. Three of the 36 mutants were shown to contain amber mutations through the use of a temperature-sensitive amber suppressor. These mutations, which mapped between gyrB and tna, were characterized genetically and biochemically as amber mutations in dnaA.

Links

PubMed PMC217197

Keywords

Bacterial Proteins/biosynthesis; Bacterial Proteins/genetics; Chromosome Mapping; DNA Replication; DNA, Bacterial/genetics; Escherichia coli/genetics; Genes; Genetic Complementation Test; Mutation; Transduction, Genetic

Main Points of the Paper

Please summarize the main points of the paper.

  • 3 amber mutations in dnaA were isolated and characterized

Materials and Methods Used

Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).

  • Conditional Integrative Suppression
  • This paper includes an extensive strain list
  • P1 transduction
  • Localized mutagenesis of the dnaA region (described elsewhere)
  • lambda21 dnaA Spi- specialized transducing phage

Phenotype Annotations

See Help:AnnotationTable for details on how to edit this table.
<protect>

Phenotype of Taxon Information Genotype Information (if known) Condition Information OMP ID OMP Term Name ECO ID ECO Term Name Notes Status

a mutation or genetic difference within a strain

  • Taxon: Escherichia coli
  • Strain: K-12
  • Substrain: NS473
  • NCBI Taxon ID: 83333
  • Genotype of Reference Strain: dnaA+
  • Genotype of Experimental Strain : dnaA311(Am)
  • Reference Condition:

0000271

temperature-dependent growth

0000178

in vivo assay evidence

reduced rate of DNA synthesis in high temperature. See figure 4A for experimental results.

a mutation or genetic difference within a strain

  • Taxon: Escherichia coli
  • Strain: K-12
  • Substrain: NS473
  • NCBI Taxon ID: 83333
  • Genotype of Reference Strain: dnaA+
  • Genotype of Experimental Strain : dnaA366(Am)
  • Reference Condition:

0000271

temperature-dependent growth

0000178

in vivo assay evidence

reduced rate of DNA synthesis in high temperature. See figure 4B for experimental results.

a mutation or genetic difference within a strain

  • Taxon: Escherichia coli
  • Strain: K-12
  • Substrain: NS473
  • NCBI Taxon ID: 83333
  • Genotype of Reference Strain: dnaA+
  • Genotype of Experimental Strain : dnaA367(Am)
  • Reference Condition:

0000271

temperature-dependent growth

0000178

in vivo assay evidence

reduced rate of DNA synthesis in high temperature. See figure 4C for experimental results.


</protect>

Notes

References

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