Difference between revisions of "PMID:14430363"

From omp dev
Jump to: navigation, search
(Main Points of the Paper)
(Table edited by Azweifel via TableEdit)
Line 70: Line 70:
 
|-
 
|-
 
!|Species!!Taxon ID!!Strain!!Gene (if known)!!OMP!!Phenotype!!Details!!Evidence!!Notes
 
!|Species!!Taxon ID!!Strain!!Gene (if known)!!OMP!!Phenotype!!Details!!Evidence!!Notes
 +
|-
 +
|
 +
''Escherichia coli''
 +
|
 +
NCBI:562
 +
|
 +
lacZ- lacI-
 +
|
 +
 +
|
 +
constitutive expression of beta-galactosidase
 +
|
 +
Metabolic Activity
 +
|
 +
lac genes were transferred from Hfr (z+i+) into F- (z-i-) during conjugation and LacZ production became constitutive within the first few minutes after transfer
 +
|
 +
Biochemical Assay
 +
|
 +
Figure 1- curves A and B (LacZ assay)
 +
|-
 +
|
 +
''Escherichia coli''
 +
|
 +
NCBI:562
 +
|
 +
lacZ- lacI-
 +
|
 +
 +
|
 +
inducible expression of beta-galactosidase
 +
|
 +
Metabolic Activity
 +
|
 +
lac genes were transferred from Hfr (z+i+) into F- (z-i-) during conjugation and LacZ production became inducible about an hour after transfer
 +
|
 +
Biochemical Assay
 +
|
 +
Figure 1- curve A vs. curve B (LacZ assay)
  
 
|- class="tableEdit_footer"  
 
|- class="tableEdit_footer"  

Revision as of 15:54, 8 December 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 observations 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

Escherichia coli

NCBI:562

lacZ- lacI-

constitutive expression of beta-galactosidase

Metabolic Activity

lac genes were transferred from Hfr (z+i+) into F- (z-i-) during conjugation and LacZ production became constitutive within the first few minutes after transfer

Biochemical Assay

Figure 1- curves A and B (LacZ assay)

Escherichia coli

NCBI:562

lacZ- lacI-

inducible expression of beta-galactosidase

Metabolic Activity

lac genes were transferred from Hfr (z+i+) into F- (z-i-) during conjugation and LacZ production became inducible about an hour after transfer

Biochemical Assay

Figure 1- curve A vs. curve B (LacZ assay)

</protect>

Notes