Difference between revisions of "PMID:3543211"

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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
 
!|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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*Taxon: Escherichia coli
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*Strain: K-12
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*Substrain: RYC714
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*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: ''sbmA<sup>+</sup>''
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*Genotype of Experimental Strain : ''BM11 sbmA11''::Tn5
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*Reference Condition:
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0000276
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increased resistance to antibiotics
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0000033
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traceable author statement
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Insertion of transposon into ''sbmA'' gene increased the occurrence Microcin B17. 
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Revision as of 19:12, 29 May 2012

Citation

Laviña, M, Pugsley, AP and Moreno, F (1986) Identification, mapping, cloning and characterization of a gene (sbmA) required for microcin B17 action on Escherichia coli K12.J. Gen. Microbiol. 132:1685-93

Abstract

We have identified mutations in three different chromosomal genes of Escherichia coli K12 which reduce sensitivity to microcin B17. Mutations in ompF and ompR genes affected production of an outer membrane porin protein, OmpF, and resulted in reduced sensitivity to a number of other agents (colicins, bacteriophages) besides microcin B17. The third class of mutants were specifically and highly resistant to microcin B17. The mutations in these strains were mapped to a gene (sbmA), located at 8.7 min on the E. coli K12 chromosome, which is closely linked to phoA. The wild-type sbmA allele was cloned into multiple copy number plasmids, and its location within the cloned DNA fragment was further defined by mutagenesis with MiniMudII1681. These insertion mutations resulted in in-frame fusions between the sbmA and lacZ genes, thereby allowing us to determine the direction of sbmA gene transcription. Plasmids carrying these gene fusions produced low levels of beta-galactosidase, indicating that the sbmA gene is poorly expressed. We have been unable to identify the sbmA gene product, but indirect evidence indicates that it might be an envelope protein involved in microcin uptake.

Links

PubMed

Keywords

Anti-Bacterial Agents; Bacteriocins; Chromosome Mapping; Cloning, Molecular; Escherichia coli; Genes, Bacterial; Mutation; Phenotype; 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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Phenotype of Taxon Information Genotype Information (if known) Condition Information OMP ID OMP Term Name ECO ID ECO Term Name Notes Status

a mutation or genetic difference within a strain

  • Taxon: Escherichia coli
  • Strain: K-12
  • Substrain: RYC714
  • NCBI Taxon ID: 83333
  • Genotype of Reference Strain: sbmA+
  • Genotype of Experimental Strain : BM11 sbmA11::Tn5
  • Reference Condition:

0000276

increased resistance to antibiotics

0000033

traceable author statement

Insertion of transposon into sbmA gene increased the occurrence Microcin B17.


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Notes

References

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