Difference between revisions of "PMID:7009581"
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Mutation the ''phosT'' gene caused resistance to arsenate resistance. | Mutation the ''phosT'' gene caused resistance to arsenate resistance. | ||
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+ | a mutation or genetic difference within a strain | ||
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+ | *Taxon: Escherichia coli | ||
+ | *Strain: K-12 | ||
+ | *Substrain: 188 | ||
+ | *NCBI Taxon ID: [http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=83333&lvl=3&lin=f&keep=1&srchmode=1&unlock 83333] | ||
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+ | *Genotype of Reference Strain: ''tolPAB<sup>+</sup>'' | ||
+ | *Genotype of Experimental Strain : ''tolPAB<sup>-</sup>'' in 207c | ||
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+ | *Reference Condition: | ||
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+ | 0000181 | ||
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+ | in vitro assay evidence | ||
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+ | The distribution of alkaline phosphatase activity within perplasmic leaky mutants showed that the remaining intracellular enzyme could be released by osmotic shock. | ||
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Revision as of 17:51, 1 October 2012
Citation |
Lazzaroni, JC and Portalier, RC (1981) Genetic and biochemical characterization of periplasmic-leaky mutants of Escherichia coli K-12. J. Bacteriol. 145:1351-8 |
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Abstract |
Periplasmic-leaky mutants of Escherichia coli K-12 were isolated after nitrosoguanidine-induced mutagenesis. They released periplasmic enzymes into the extracellular medium. Excretion of alkaline phosphatase, which started immediately in the early exponential phase of growth, could reach up to 90% of the total enzyme production in the stationary phase. Leaky mutants were sensitive to ethylenediaminetetraacetic acid, cholic acid, and the antibiotics rifampin, chloramphenicol, mitomycin C, and ampicillin. Furthermore, they were resistant to colicin E1 and partially resistant to phage TuLa. Their genetic characterization showed that the lky mutations mapped between the suc and gal markers, near or in the tolPAB locus. A biochemical analysis of cell envelope components showed that periplasmic-leaky mutants contained reduced amounts of major outer membrane protein OmpF and increased amounts of a 16,000-dalton outer membrane protein. |
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Keywords |
Alkaline Phosphatase/metabolism; Bacterial Proteins/metabolism; Cell Membrane/physiology; Chromosome Mapping; Chromosomes, Bacterial; Escherichia coli/genetics; Escherichia coli/physiology; Genes; Membrane Proteins/metabolism; Mutation |
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Main Points of the Paper
Please summarize the main points of the paper.
Materials and Methods Used
Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).
Phenotype Annotations
See Help:AnnotationTable for details on how to edit this table.
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Phenotype of | Taxon Information | Genotype Information (if known) | Condition Information | OMP ID | OMP Term Name | ECO ID | ECO Term Name | Notes | Status |
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a mutation or genetic difference within a strain |
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0000085 |
cell envelope phenotype |
0000181 |
in vitro assay evidence |
A mutation in the strain 207's tolPAB operon caused the exretion of alakaline phosphate, RNAase I and DNAse I. |
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a mutation or genetic difference within a strain |
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0000181 |
in vitro assay evidence |
Mutation the phosT gene caused resistance to arsenate resistance. |
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a mutation or genetic difference within a strain |
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0000085 |
cell envelope phenotype |
0000181 |
in vitro assay evidence |
A mutation in the strain 236's tolPAB operon caused the exretion of alakaline phosphate, RNAase I and DNAse I. |
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a mutation or genetic difference within a strain |
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0000181 |
in vitro assay evidence |
Mutation the phosT gene caused resistance to arsenate resistance. |
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a mutation or genetic difference within a strain |
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0000181 |
in vitro assay evidence |
Mutation the tolPAB gene caused increased activity of alkaline phosphatase. See Figure 1. |
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a mutation or genetic difference within a strain |
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0000181 |
in vitro assay evidence |
Mutation the tolPAB gene caused increased activity of alkaline phosphatase. See Figure 1. |
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a mutation or genetic difference within a strain |
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|
|
0000181 |
in vitro assay evidence |
Mutation the phosT gene caused resistance to arsenate resistance. |
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a mutation or genetic difference within a strain |
|
|
|
0000181 |
in vitro assay evidence |
The distribution of alkaline phosphatase activity within perplasmic leaky mutants showed that the remaining intracellular enzyme could be released by osmotic shock. |
| ||
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</protect>
Notes
References
See Help:References for how to manage references in omp dev.