Difference between revisions of "PMID:4567134"
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+ | {| id="S5776ad28a29d1" class=" tableEdit PMID_info_table" | ||
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+ | |- | ||
+ | !align=left align='left' bgcolor='#CCCCFF' |Citation | ||
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+ | '''Silverman, M and Simon, M''' (1973) Genetic analysis of flagellar mutants in Escherichia coli. ''J. Bacteriol.'' '''113''':105-13 | ||
+ | |- | ||
+ | !align=left align='left' bgcolor='#CCCCFF' |Abstract | ||
+ | || | ||
+ | Flagellar mutants in Escherichia coli were obtained by selection for resistance to the flagellotropic phage chi. F elements covering various regions of the E. coli genome were then constructed, and, on the basis of the ability of these elements to restore flagellar function, the mutations were assigned to three regions of the E. coli chromosome. Region I is between trp and gal; region II is between uvrC and aroD; and region III is between his and uvrC. F elements carrying flagellar mutations were constructed. Stable merodiploid strains with a flagellar defect on the exogenote and another on the endogenote were then prepared. These merodiploids yielded information on the complementation behavior of mutations in a given region. Region III was shown to include at least six cistrons, A, B, C, D, E, and F. Region II was shown to include at least four cistrons, G, H, I, and J. Examination of the phenotypes of the mutants revealed that those with lesions in cistron E of region III produce "polyhooks" and lesions in cistron F of region III result in loss of ability to produce flagellin. Mutants with lesions in cistron J of region II were entirely paralyzed (mot) mutants. Genetic analysis of flagellar mutations in region III suggested that the mutations located in cistrons A, B, C, and E are closely linked and mutations in cistrons D and F are closely linked. | ||
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+ | !align=left align='left' bgcolor='#CCCCFF' |Links | ||
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+ | [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=4567134 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC251608 PMC251608] | ||
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+ | |- | ||
+ | !align=left align='left' bgcolor='#CCCCFF' |Keywords | ||
+ | || | ||
+ | Antigens, Bacterial; Bacterial Proteins/biosynthesis; Chromosome Mapping; Chromosomes, Bacterial; Coliphages; Diploidy; Escherichia coli/cytology; Escherichia coli/immunology; Escherichia coli/metabolism; Flagella/immunology; Flagella/metabolism; Genetic Complementation Test; Genetic Techniques; Lysogeny; Microscopy, Electron; Mutation; Phenotype; Recombination, Genetic; Transduction, Genetic | ||
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+ | ==Main Points of the Paper == | ||
+ | {{LitSignificance}} | ||
+ | |||
+ | == Materials and Methods Used == | ||
+ | {{LitMaterials}} | ||
+ | |||
+ | ==Phenotype Annotations== | ||
+ | {{AnnotationTableHelp}} | ||
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+ | <!-- | ||
+ | ****************************************************************************************** | ||
+ | * | ||
+ | * ** PLEASE DON'T EDIT THIS TABLE DIRECTLY. Use the edit table link under the table. ** | ||
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+ | |- align='left' bgcolor='#CCCCFF' | ||
+ | !|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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+ | |} | ||
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+ | <!--box uid=d41d8cd98f00b204e9800998ecf8427e.8099.S5776ad28bedf4--></protect> | ||
+ | |||
+ | ==Notes== | ||
+ | |||
+ | ==References== | ||
+ | {{RefHelp}} | ||
+ | <references/> | ||
+ | |||
+ | |||
+ | [[Category:Publication]] |
Latest revision as of 12:49, 1 July 2016
Citation |
Silverman, M and Simon, M (1973) Genetic analysis of flagellar mutants in Escherichia coli. J. Bacteriol. 113:105-13 |
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Abstract |
Flagellar mutants in Escherichia coli were obtained by selection for resistance to the flagellotropic phage chi. F elements covering various regions of the E. coli genome were then constructed, and, on the basis of the ability of these elements to restore flagellar function, the mutations were assigned to three regions of the E. coli chromosome. Region I is between trp and gal; region II is between uvrC and aroD; and region III is between his and uvrC. F elements carrying flagellar mutations were constructed. Stable merodiploid strains with a flagellar defect on the exogenote and another on the endogenote were then prepared. These merodiploids yielded information on the complementation behavior of mutations in a given region. Region III was shown to include at least six cistrons, A, B, C, D, E, and F. Region II was shown to include at least four cistrons, G, H, I, and J. Examination of the phenotypes of the mutants revealed that those with lesions in cistron E of region III produce "polyhooks" and lesions in cistron F of region III result in loss of ability to produce flagellin. Mutants with lesions in cistron J of region II were entirely paralyzed (mot) mutants. Genetic analysis of flagellar mutations in region III suggested that the mutations located in cistrons A, B, C, and E are closely linked and mutations in cistrons D and F are closely linked. |
Links | |
Keywords |
Antigens, Bacterial; Bacterial Proteins/biosynthesis; Chromosome Mapping; Chromosomes, Bacterial; Coliphages; Diploidy; Escherichia coli/cytology; Escherichia coli/immunology; Escherichia coli/metabolism; Flagella/immunology; Flagella/metabolism; Genetic Complementation Test; Genetic Techniques; Lysogeny; Microscopy, Electron; Mutation; Phenotype; Recombination, Genetic; Transduction, Genetic |
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
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<protect>
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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</protect>
Notes
References
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