Literature DB >> 2144273

Isolation and characterization of dnaJ null mutants of Escherichia coli.

S M Sell1, C Eisen, D Ang, M Zylicz, C Georgopoulos.   

Abstract

Bacteriophage lambda requires the lambda O and P proteins for its DNA replication. The rest of the replication proteins are provided by the Escherichia coli host. Some of these host proteins, such as DnaK, DnaJ, and GrpE, are heat shock proteins. Certain mutations in the dnaK, dnaJ, or grpE gene block lambda growth at all temperatures and E. coli growth above 43 degrees C. We have isolated bacterial mutants that were shown by Southern analysis to contain a defective, mini-Tn10 transposon inserted into either of two locations and in both orientations within the dnaJ gene. We have shown that these dnaJ-insertion mutants did not grow as well as the wild type at temperatures above 30 degrees C, although they blocked lambda DNA replication at all temperatures. The dnaJ-insertion mutants formed progressively smaller colonies at higher temperatures, up to 42 degrees C, and did not form colonies at 43 degrees C. The accumulation of frequent, uncharacterized suppressor mutations allowed these insertion mutants to grow better at all temperatures and to form colonies at 43 degrees C. None of these suppressor mutations restored the ability of the host to propagate phage lambda. Radioactive labeling of proteins synthesized in vivo followed by immunoprecipitation or immunoblotting with anti-DnaJ antibodies demonstrated that no DnaJ protein could be detected in these mutants. Labeling studies at different temperatures demonstrated that these dnaJ-insertion mutations resulted in altered kinetics of heat shock protein synthesis. An additional eight dnaJ mutant isolates, selected spontaneously on the basis of blocking phage lambda growth at 42 degrees C, were shown not to synthesize DnaJ protein as well. Three of these eight spontaneous mutants had gross DNA alterations in the dnaJ gene. Our data provide evidence that the DnaJ protein is not absolutely essential for E. coli growth at temperatures up to 42 degrees C under standard laboratory conditions but is essential for growth at 43 degrees C. However, the accumulation of extragenic suppressors is necessary for rapid bacterial growth at higher temperatures.

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Year:  1990        PMID: 2144273      PMCID: PMC213136          DOI: 10.1128/jb.172.9.4827-4835.1990

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  40 in total

1.  Cellular defects caused by deletion of the Escherichia coli dnaK gene indicate roles for heat shock protein in normal metabolism.

Authors:  B Bukau; G C Walker
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

2.  High resolution two-dimensional electrophoresis of proteins.

Authors:  P H O'Farrell
Journal:  J Biol Chem       Date:  1975-05-25       Impact factor: 5.157

3.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Authors:  H Towbin; T Staehelin; J Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

4.  Organization and expression of the dnaJ and dnaK genes of Escherichia coli K12.

Authors:  H Saito; H Uchida
Journal:  Mol Gen Genet       Date:  1978-08-04

5.  Initiation of the DNA replication of bacteriophage lambda in Escherichia coli K12.

Authors:  H Saito; H Uchida
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

6.  Genetic analysis of two genes, dnaJ and dnaK, necessary for Escherichia coli and bacteriophage lambda DNA replication.

Authors:  J Yochem; H Uchida; M Sunshine; H Saito; C P Georgopoulos; M Feiss
Journal:  Mol Gen Genet       Date:  1978-08-04

7.  Participation of Escherichia coli heat shock proteins DnaJ, DnaK, and GrpE in P1 plasmid replication.

Authors:  K Tilly; M Yarmolinsky
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

8.  Escherichia coli DnaK and GrpE heat shock proteins interact both in vivo and in vitro.

Authors:  C Johnson; G N Chandrasekhar; C Georgopoulos
Journal:  J Bacteriol       Date:  1989-03       Impact factor: 3.490

9.  The heat-shock-regulated grpE gene of Escherichia coli is required for bacterial growth at all temperatures but is dispensable in certain mutant backgrounds.

Authors:  D Ang; C Georgopoulos
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

10.  Initiation of lambda DNA replication with purified host- and bacteriophage-encoded proteins: the role of the dnaK, dnaJ and grpE heat shock proteins.

Authors:  M Zylicz; D Ang; K Liberek; C Georgopoulos
Journal:  EMBO J       Date:  1989-05       Impact factor: 11.598

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  39 in total

1.  The djlA gene acts synergistically with dnaJ in promoting Escherichia coli growth.

Authors:  P Genevaux; F Schwager; C Georgopoulos; W L Kelley
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

2.  A novel Campylobacter jejuni two-component regulatory system important for temperature-dependent growth and colonization.

Authors:  A M Brás; S Chatterjee; B W Wren; D G Newell; J M Ketley
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

3.  DnaK-facilitated ribosome assembly in Escherichia coli revisited.

Authors:  Jean-Hervé Alix; Knud H Nierhaus
Journal:  RNA       Date:  2003-07       Impact factor: 4.942

4.  Levels of epsilon, an essential replication subunit of Escherichia coli DNA polymerase III, are controlled by heat shock proteins.

Authors:  P L Foster; M G Marinus
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

5.  Cooperation of GroEL/GroES and DnaK/DnaJ heat shock proteins in preventing protein misfolding in Escherichia coli.

Authors:  A Gragerov; E Nudler; N Komissarova; G A Gaitanaris; M E Gottesman; V Nikiforov
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-01       Impact factor: 11.205

Review 6.  Heat shock protein 70 (hsp70) as an emerging drug target.

Authors:  Christopher G Evans; Lyra Chang; Jason E Gestwicki
Journal:  J Med Chem       Date:  2010-06-24       Impact factor: 7.446

7.  The DnaK chaperone modulates the heat shock response of Escherichia coli by binding to the sigma 32 transcription factor.

Authors:  K Liberek; T P Galitski; M Zylicz; C Georgopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-15       Impact factor: 11.205

8.  The Escherichia coli DjlA and CbpA proteins can substitute for DnaJ in DnaK-mediated protein disaggregation.

Authors:  Eyal Gur; Dvora Biran; Nelia Shechter; Pierre Genevaux; Costa Georgopoulos; Eliora Z Ron
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

9.  The RpoH-mediated stress response in Neisseria gonorrhoeae is regulated at the level of activity.

Authors:  Lina Laskos; Catherine S Ryan; Janet A M Fyfe; John K Davies
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

10.  Molecular chaperones facilitate the soluble expression of N-acyl-D-amino acid amidohydrolases in Escherichia coli.

Authors:  Kazuaki Yoshimune; Yoko Ninomiya; Mamoru Wakayama; Mitsuaki Moriguchi
Journal:  J Ind Microbiol Biotechnol       Date:  2004-08-28       Impact factor: 3.346

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