Literature DB >> 6097795

Physical and genetic structure of the glpK-cpxA interval of the Escherichia coli K-12 chromosome.

R Albin, P M Silverman.   

Abstract

Mutations at the cpxA locus of Escherichia coli K-12 affect cellular processes that are not otherwise related. We have now determined the physical and genetic structure of the E. coli chromosome in the region of cpxA (87.5 min). Our results indicate that cpxA is a single gene. Previous studies showed cpxA to be linked to tpiA. We therefore isolated two tpiA+ recombinant plasmids, pRA200 and pRA300, from EcoRI and BamHI digests of F'133, respectively. By genetic complementation or enzyme overproduction, the 9.5 kb EcoRI fragment in pRA200 was shown to include glpK, tpiA and cdh. The 13.6 kb BamHI fragment of pRA300 lacks glpK, but includes tpiA, pfkA and cpxA. Neither fragment complemented a deletion of the rha operon. These data indicate the chromosomal gene order: 87 min-rha-cpxA-pfkA-cdh-tpiA-glpK-88 min. The EcoRI and BamHI fragments overlap in an interval corresponding to about 8.2 kb of DNA. The total region of the E. coli K12 chromosome covered by the two fragments is about 15 kb. A terminal 2 kb EcoRI-BamHI fragment from pRA300 complemented the chromosomal cpxA2[Ts] allele with respect to isoleucine and valine synthesis, RNA bacteriophage sensitivity and surface exclusion in Hfr strains, and envelope protein composition. Complementation occurred when the fragment was subcloned in pBR325 but not when it was subcloned in pBR322, suggesting that the 2 kb fragment lacks expression sequences that are supplied by cat (chloramphenicol acetyltransferase gene) expression sequences of pBR325. The cpxA locus on the E. coli chromosome was established with respect to two chromosomal Tn10 insertions by a combination of genetic and physical analyses. The locus established by those analyses was consistent with the location of the 2 kb EcoRI-BamHI fragment in the physical map of the region. Physical analyses of (rha-pfkA) and (rha-tpiA) deletion strains showed that they lack cpxA and surrounding genes. Since these strains were viable, cpxA is not essential under all growth conditions.

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Year:  1984        PMID: 6097795     DOI: 10.1007/bf00330972

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  36 in total

1.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

2.  Deletion mapping of the polA-metB region of the Escherichia coli chromosome.

Authors:  G Pahel; F R Bloom; B Tyler
Journal:  J Bacteriol       Date:  1979-05       Impact factor: 3.490

3.  Method for obtaining more-accurate covalently closed circular plasmid-to-chromosome ratios from bacterial lysates by dye-buoyant density centrifugation.

Authors:  D D Womble; D P Taylor; R H Rownd
Journal:  J Bacteriol       Date:  1977-04       Impact factor: 3.490

4.  A simple method for the preparation of large quantities of pure plasmid DNA.

Authors:  G O Humphreys; G A Willshaw; E S Anderson
Journal:  Biochim Biophys Acta       Date:  1975-04-02

5.  Restriction enzyme cleavage map of Tn10, a transposon which encodes tetracycline resistance.

Authors:  R A Jorgensen; D E Berg; B Allet; W S Reznikoff
Journal:  J Bacteriol       Date:  1979-01       Impact factor: 3.490

6.  Regulation of the F conjugation genes studied by hybridization and tra-lacZ fusion.

Authors:  D Gaffney; R Skurray; N Willetts
Journal:  J Mol Biol       Date:  1983-07-25       Impact factor: 5.469

7.  Map location of the ssd mutation in Escherichia coli K-12.

Authors:  J F Morris; E B Newman
Journal:  J Bacteriol       Date:  1980-09       Impact factor: 3.490

8.  Mutations in genes cpxA and cpxB of Escherichia coli K-12 cause a defect in acetohydroxyacid synthase I function in vivo.

Authors:  A Sutton; T Newman; J McEwen; P M Silverman; M Freundlich
Journal:  J Bacteriol       Date:  1982-08       Impact factor: 3.490

9.  Application of hybrid plasmids carrying glycolysis genes to ATP production by Escherichia coli.

Authors:  M Shimosaka; Y Fukuda; K Murata; A Kimura
Journal:  J Bacteriol       Date:  1982-10       Impact factor: 3.490

10.  Genetic analysis of Escherichia coli K-12 chromosomal mutants defective in expression of F-plasmid functions: identification of genes cpxA and cpxB.

Authors:  J McEwen; P Silverman
Journal:  J Bacteriol       Date:  1980-10       Impact factor: 3.490

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  9 in total

Review 1.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

Review 2.  Linkage map of Escherichia coli K-12, edition 8.

Authors:  B J Bachmann
Journal:  Microbiol Rev       Date:  1990-06

3.  Role of small subunit (IlvN polypeptide) of acetohydroxyacid synthase I from Escherichia coli K-12 in sensitivity of the enzyme to valine inhibition.

Authors:  L Eoyang; P M Silverman
Journal:  J Bacteriol       Date:  1986-06       Impact factor: 3.490

4.  Accumulation of the F plasmid TraJ protein in cpx mutants of Escherichia coli.

Authors:  P M Silverman; L Tran; R Harris; H M Gaudin
Journal:  J Bacteriol       Date:  1993-02       Impact factor: 3.490

5.  Glycerol facilitator of Escherichia coli: cloning of glpF and identification of the glpF product.

Authors:  G Sweet; C Gandor; R Voegele; N Wittekindt; J Beuerle; V Truniger; E C Lin; W Boos
Journal:  J Bacteriol       Date:  1990-01       Impact factor: 3.490

6.  The Cpx two-component signal transduction pathway is activated in Escherichia coli mutant strains lacking phosphatidylethanolamine.

Authors:  E Mileykovskaya; W Dowhan
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

7.  The Cpx proteins of Escherichia coli K-12: evidence that cpxA, ecfB, ssd, and eup mutations all identify the same gene.

Authors:  S Rainwater; P M Silverman
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

8.  Identification of the Escherichia coli K-12 cpxA locus as a single gene: construction and analysis of biologically-active cpxA gene fusions.

Authors:  R Albin; P M Silverman
Journal:  Mol Gen Genet       Date:  1984

9.  Isolation of superoxide dismutase mutants in Escherichia coli: is superoxide dismutase necessary for aerobic life?

Authors:  A Carlioz; D Touati
Journal:  EMBO J       Date:  1986-03       Impact factor: 11.598

  9 in total

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