PMID:14430363: Difference between revisions

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==Main Points of the Paper ==
==Main Points of the Paper ==
*Hfr''z<sup>+</sup>i<sup>+</sup>'' x F<sup>-</sup>z<sup>-</sup>i<sup>-</sup>:  
*High Frequency recombinant(Hfr) ''z<sup>+</sup>i<sup>+</sup>'' x F<sup>-</sup>z<sup>-</sup>i<sup>-</sup>:  
**within a few minutes of the time of entry of the ''z<sup>+</sup>i<sup>+</sup>'' genes (which are closely linked) the synthesis of β-galactosidase commenced at maximal velocity in the absence of extracellular inducer
**within a few minutes of the time of entry of the ''z<sup>+</sup>i<sup>+</sup>'' genes (which are closely linked) the synthesis of β-galactosidase commenced at maximal velocity in the absence of extracellular inducer
**inducible i<sup>+</sup> allele appears dominant over the constitutive i<sup>-</sup> allele
**inducible i<sup>+</sup> allele appears dominant over the constitutive i<sup>-</sup> allele

Revision as of 22:02, 22 November 2010

Citation

PARDEE, AB and PRESTIDGE, LS (1959) On the nature of the repressor of beta-galactosidase synthesis in Escherichia coli.Biochim. Biophys. Acta 36:545-7

Abstract

No abstract in PubMed

Links

PubMed

Keywords

Escherichia coli; Glycoside Hydrolases

Main Points of the Paper

  • High Frequency recombinant(Hfr) z+i+ x F-z-i-:
    • within a few minutes of the time of entry of the z+i+ genes (which are closely linked) the synthesis of β-galactosidase commenced at maximal velocity in the absence of extracellular inducer
    • inducible i+ allele appears dominant over the constitutive i- allele
  • The authors of this paper eventually conclude that the repressor is not a protein, but evidence to refute this conclusion is shown here.

Materials and Methods Used

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

Phenotype Annotations

Species Taxon ID Strain Gene (if known) OMP Phenotype Details Evidence Notes


Notes