PMID:4887874: Difference between revisions
Table edited by Azweifel via TableEdit |
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NCBI:562 | NCBI:562 | ||
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NG545-pi(1) | NG545-pi(1) | ||
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lacZ | lacZ | ||
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NCBI:562 | NCBI:562 | ||
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NG545 | NG545 | ||
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lacZ | |||
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Growth | |||
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able to metabolize lactose only in a su<sub>I</sub><sub>+</sub> background | |||
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Plating Assay | |||
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Table 2- UAG polar mutation | |||
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''Escherichia coli'' | |||
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NCBI:562 | |||
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NG24 | |||
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lacZ | lacZ | ||
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Metabolic Activity | Metabolic Activity | ||
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4.7% of the wild type level when induced | |||
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Biochemical Assay | Biochemical Assay | ||
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Table 4 | |||
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Revision as of 22:23, 15 December 2010
| Citation |
Grodzicker, T and Zipser, D (1968) A mutation which creates a new site for the re-initiation of polypeptide synthesis in the z gene of the lac operon of Escherichia coli.J. Mol. Biol. 38:305-14 |
|---|---|
| Abstract |
No abstract in PubMed |
| Links | |
| Keywords |
Acyltransferases; Chromosome Mapping; Escherichia coli; Genes; Membrane Transport Proteins; Mutation; Operon |
| edit table |
Main Points of the Paper
- Polar effects of a UAG mutation in the operator-proximal region of the z gene are studied which leads to the isolation of two suppressor mutations
- π, a new site of initiation of protein synthesis is described
- operates efficiently to restore permease and acetylase activity to a high level when induced
- regulation/induction is still required, so the authors deduce that π is a new site of translation initiation (
- not a new site of transcriptional initiation because acetylase is not present in the absence of inducer
Materials and Methods Used
- Parent Strain: NG545 (trp-8, SmS Hfr)
- UAG mutation had not been altered in the suppressor strains isolated
- Strain: CA77B (Δlac, trp-8, SmR F-)
- Strain: X103B (Δlac pro, trp-8, SmR F-)
- Strain: M107 (Δlac, suI+, SmR F-)
- Strain: ΔLacW (Δlac, his-, SmR F-)
- Strain: E29 (lac+ , F'/lac+, threonine-, leucine-, B1-, SmR)
- Acetylase assay
- β-galactosidase assay
Phenotype Annotations
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| Species | Taxon ID | Strain | Gene (if known) | OMP | Phenotype | Details | Evidence | Notes |
|---|---|---|---|---|---|---|---|---|
|
Escherichia coli |
NCBI:562 |
NG545-pi(1)a |
lacZ |
able to metabolize melibiose |
Growth |
growth on melibiose- polar effects |
Plating Assay |
Table 2 |
|
Escherichia coli |
NCBI:562 |
NG545-pi(1) |
lacZ |
Growth |
able to metabolize lactose only in a suI+ background |
Plating Assay |
Table 2- UAG polar mutation | |
|
Escherichia coli |
NCBI:562 |
NG545-pi(1)b |
lacZ |
unable to metabolize melibiose |
Growth |
growth on melibiose-polar effects |
Plating Assay |
Table 2- |
|
Escherichia coli |
NCBI:562 |
NG545-pi(1)a |
lacZ |
reduced beta-galactosidase activity |
Metabolic Activity |
trace amounts when induced |
Biochemical Assay |
Table 2 |
|
Escherichia coli |
NCBI:562 |
NG545-pi(1)b |
lacZ |
reduced beta-galactosidase activity |
Metabolic Activity |
trace amounts when induced |
Biochemical Assay |
Table 2 |
|
Escherichia coli |
NCBI:562 |
NG545B |
lacZ |
reduced acetylase activity |
Metabolic Activity |
4.2% of the wild type level when induced |
Biochemical Assay |
Tables 3 and 4 |
|
Escherichia coli |
NCBI:562 |
NG545-pi(1) |
lacZ |
reduced acetylase activity |
Metabolic Activity |
35% of the wild type level when induced |
Biochemical Assay |
Tables 3 and 4 |
|
Escherichia coli |
NCBI:562 |
NG545 |
lacZ |
Growth |
able to metabolize lactose only in a suI+ background |
Plating Assay |
Table 2- UAG polar mutation | |
|
Escherichia coli |
NCBI:562 |
NG24 |
lacZ |
reduced acetylase activity |
Metabolic Activity |
4.7% of the wild type level when induced |
Biochemical Assay |
Table 4 |
| edit table |
Notes
References
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