Difference between revisions of "PMID:338588"
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+ | {| id="B576af7d034730" class=" tableEdit PMID_info_table" | ||
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+ | |- | ||
+ | !align=left align='left' bgcolor='#CCCCFF' |Citation | ||
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+ | '''Komeda, Y, Silverman, M and Simon, M''' (1978) Identification of the structural gene for the hook subunit protein of Escherichia coli flagella. ''J. Bacteriol.'' '''133''':364-71 | ||
+ | |- | ||
+ | !align=left align='left' bgcolor='#CCCCFF' |Abstract | ||
+ | || | ||
+ | Previous studies showed that the structural gene for the flagellar hook subunit protein (molecular weight 42,000) was one of a group of flagellar genes located on the Escherichia coli genome near pyrC. Several lines of evidence indicate that the flaK gene is the structural gene for the hook subunit protein. Fla+ strains that were insensitive to chi infection could be isolated as revertants of an FlaK- amber mutant strain but from no other Fla- strain. The hook subunit proteins isolated from such chi-sensitive revertants of the FlaK- strain were shown to be antigenically and electrophoretically different from the hook protein isolated from the wild-type strain. Thus, reversion of a mutation in the flaK gene resulted in alteration of the structure of the hook protein. Furthermore, in programming experiments with hybrid lambda containing flagellar genes, lambdafla with flaK genetic activity programmed the synthesis of a 42,000-molecular weight protein, whereas lambdafla without flaK genetic activity did not. | ||
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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=338588 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC222015 PMC222015] | ||
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+ | |- | ||
+ | !align=left align='left' bgcolor='#CCCCFF' |Keywords | ||
+ | || | ||
+ | Bacterial Proteins/genetics; Bacterial Proteins/immunology; Chromosome Mapping; Coliphages; Escherichia coli/genetics; Flagella/metabolism; Genes; Mutation; Phenotype; Recombination, Genetic | ||
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+ | ==Main Points of the Paper == | ||
+ | {{LitSignificance}} | ||
+ | |||
+ | == Materials and Methods Used == | ||
+ | {{LitMaterials}} | ||
+ | |||
+ | ==Phenotype Annotations== | ||
+ | {{AnnotationTableHelp}} | ||
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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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+ | |||
+ | ==Notes== | ||
+ | |||
+ | ==References== | ||
+ | {{RefHelp}} | ||
+ | <references/> | ||
+ | |||
+ | |||
+ | [[Category:Publication]] |
Latest revision as of 15:40, 22 June 2016
Citation |
Komeda, Y, Silverman, M and Simon, M (1978) Identification of the structural gene for the hook subunit protein of Escherichia coli flagella. J. Bacteriol. 133:364-71 |
---|---|
Abstract |
Previous studies showed that the structural gene for the flagellar hook subunit protein (molecular weight 42,000) was one of a group of flagellar genes located on the Escherichia coli genome near pyrC. Several lines of evidence indicate that the flaK gene is the structural gene for the hook subunit protein. Fla+ strains that were insensitive to chi infection could be isolated as revertants of an FlaK- amber mutant strain but from no other Fla- strain. The hook subunit proteins isolated from such chi-sensitive revertants of the FlaK- strain were shown to be antigenically and electrophoretically different from the hook protein isolated from the wild-type strain. Thus, reversion of a mutation in the flaK gene resulted in alteration of the structure of the hook protein. Furthermore, in programming experiments with hybrid lambda containing flagellar genes, lambdafla with flaK genetic activity programmed the synthesis of a 42,000-molecular weight protein, whereas lambdafla without flaK genetic activity did not. |
Links | |
Keywords |
Bacterial Proteins/genetics; Bacterial Proteins/immunology; Chromosome Mapping; Coliphages; Escherichia coli/genetics; Flagella/metabolism; Genes; Mutation; Phenotype; Recombination, 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
See Help:AnnotationTable for details on how to edit this table.
<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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