Difference between revisions of "PMID:14430363"

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(Main Points of the Paper)
(Materials and Methods Used)
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== Materials and Methods Used ==
 
== Materials and Methods Used ==
{{LitMaterials}}
+
*Strains:
 +
**Hfr (''z<sup>+</sup>i<sup>+</sup>)
 +
**F<sup>-</sup> (z<sup>-</sup>i<sup>-</sup>)
 +
 
 +
*Conjugation
 +
 
 +
*Reagents
 +
**Streptomycin
 +
**Chloramphenicol
 +
**5-methytryptophan
 +
**Duponol C(Na lauryl sulfate)
  
 
==Phenotype Annotations==
 
==Phenotype Annotations==

Revision as of 17:29, 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

  • 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 idea that i+ could control the synthesis of a destructive enzyme which removes an endogenous intracellular inducer was eliminated due to observation from this paper (Figure 1, curves C & D).
  • The presence of 5-methyltryptophan enhances mating efficiency
  • The data in this paper may suggest that:
    • an inducer-destroying enzyme is not responsible for the difference between inducibility and constitutivity
    • the repressor is not a protein, although the authors state this conclusion is open to doubt (evidence to refute this conclusion is shown here).

Materials and Methods Used

  • Strains:
    • Hfr (z+i+)
    • F- (z-i-)
  • Conjugation
  • Reagents
    • Streptomycin
    • Chloramphenicol
    • 5-methytryptophan
    • Duponol C(Na lauryl sulfate)

Phenotype Annotations

<protect>

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

</protect>

Notes