Difference between revisions of "PMID:14430363"

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(Main Points of the Paper)
(Main Points of the Paper)
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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>:
 +
**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
 +
 
*The authors of this paper eventually conclude that the repressor is not a protein, but evidence to refute this conclusion is shown [[PMID:5330222|here]].
 
*The authors of this paper eventually conclude that the repressor is not a protein, but evidence to refute this conclusion is shown [[PMID:5330222|here]].
  

Revision as of 17:01, 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

  • Hfrz+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

<protect>

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

</protect>

Notes