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>: | |||
**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 22:01, 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 |
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| Abstract |
No abstract in PubMed |
| Links | |
| Keywords |
Escherichia coli; Glycoside Hydrolases |
| edit table |
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
| Species | Taxon ID | Strain | Gene (if known) | OMP | Phenotype | Details | Evidence | Notes |
|---|---|---|---|---|---|---|---|---|
| edit table |
