PMID:2835636: Difference between revisions

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<span style = 'font-size: large'> '''Fukuda, R, Nishimura, A and Serizawa, H'''  (1988) Genetic mapping of the Escherichia coli gene for the stringent starvation protein and its dispensability for normal cell growth.''Mol. Gen. Genet.'' '''211''':515-9</span>
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!align=left  |Citation
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'''No author listed'''  (1988) Genetic mapping of the Escherichia coli gene for the stringent starvation protein and its dispensability for normal cell growth. ''Mol. Gen. Genet.'' '''211''':515-9
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!align=left  |Abstract
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To determine its map position, the sSP gene was cloned into plasmid pBR322 and the recombinant plasmid was integrated into the chromosome of a polA mutant at the site of the sSP gene by homologous recombination. The chromosomal location of Ampr was then determined by P1 phage-mediated transduction. Thus, the sSP gene was mapped between gltB and glnF at min 69.5 on the Escherichia coli chromosome. Strains were constructed in which the sSP gene was brought under the control of the lac regulatory system. This indicated that the stringent starvation protein (SSP) is dispensable for growth, at least under normal culture conditions.
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!align=left  |Links
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=2835636 PubMed]


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|{{TableHeadingColor}} |'''Abstract''' || To determine its map position, the sSP gene was cloned into plasmid pBR322 and the recombinant plasmid was integrated into the chromosome of a polA mutant at the site of the sSP gene by homologous recombination. The chromosomal location of Ampr was then determined by P1 phage-mediated transduction. Thus, the sSP gene was mapped between gltB and glnF at min 69.5 on the Escherichia coli chromosome. Strains were constructed in which the sSP gene was brought under the control of the lac regulatory system. This indicated that the stringent starvation protein (SSP) is dispensable for growth, at least under normal culture conditions.
!align=left  |Keywords
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Bacterial Proteins/genetics; Base Sequence; Chromosome Mapping; Chromosomes, Bacterial/physiology; DNA Restriction Enzymes; Escherichia coli/genetics; Escherichia coli/growth & development; Genes; Genes, Bacterial; Molecular Sequence Data; Plasmids
|{{TableHeadingColor}} nowrap |'''Links''' ||  [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=2835636 PubMed]
 
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==Significance {{HelpIcon|Help:Literature}} ==
==Significance {{HelpIcon|Help:Literature}} ==
{{LitSignificance}}
{{LitSignificance}}

Revision as of 19:20, 1 September 2013

Citation

No author listed (1988) Genetic mapping of the Escherichia coli gene for the stringent starvation protein and its dispensability for normal cell growth. Mol. Gen. Genet. 211:515-9

Abstract

To determine its map position, the sSP gene was cloned into plasmid pBR322 and the recombinant plasmid was integrated into the chromosome of a polA mutant at the site of the sSP gene by homologous recombination. The chromosomal location of Ampr was then determined by P1 phage-mediated transduction. Thus, the sSP gene was mapped between gltB and glnF at min 69.5 on the Escherichia coli chromosome. Strains were constructed in which the sSP gene was brought under the control of the lac regulatory system. This indicated that the stringent starvation protein (SSP) is dispensable for growth, at least under normal culture conditions.

Links

PubMed

Keywords

Bacterial Proteins/genetics; Base Sequence; Chromosome Mapping; Chromosomes, Bacterial/physiology; DNA Restriction Enzymes; Escherichia coli/genetics; Escherichia coli/growth & development; Genes; Genes, Bacterial; Molecular Sequence Data; Plasmids

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Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status
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