Literature DB >> 6092838

Isolation and physical mapping of temperature-sensitive mutants defective in heat-shock induction of proteins in Escherichia coli.

T Tobe, K Ito, T Yura.   

Abstract

Mutants of Escherichia coli K12 that are partially or totally defective in induction of major heat-shock proteins and cannot grow at high temperature (42 degrees C) were isolated by localized mutagenesis. These mutants carry a single mutation in the gene htp R (formerly hin) located at min 76 on the E. coli genetic map. Some mutants exhibit delayed (partial) induction of heat-shock proteins or require a higher temperature for induction than the wild type, whereas others are not induced under any of these conditions. The maximum temperature that allows growth varies among different mutants and is correlated with the residual induction capacity. Temperature-resistant revertants obtained from each mutant are fully or partially recovered in heat-shock induction. These results indicate that the inability of htp R mutants to grow at high temperature is due to the defect in heat-shock induction. In addition, a couple of mutants was found that produce significantly higher amounts of heat-shock proteins even at 30 degrees C. The htp R gene has been cloned into plasmid pBR322 using the above mutants, and was localized to a DNA segment of 1.6 kilobase pairs. The mutants harboring certain plasmids that carry a part of htp R produce temperature-resistant recombinants at high frequency. This permits further localization of mutations within the htp R gene. Analysis of proteins encoded by each of the recombinant plasmids including the one carrying a previously isolated amber mutation (htp R165) led to the identification of a protein with an apparent molecular weight of about 36,000 daltons as the htp R gene product.

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Year:  1984        PMID: 6092838     DOI: 10.1007/bf00332716

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


  16 in total

1.  Acetylornithinase of Escherichia coli: partial purification and some properties.

Authors:  H J VOGEL; D M BONNER
Journal:  J Biol Chem       Date:  1956-01       Impact factor: 5.157

2.  Simple method for identification of plasmid-coded proteins.

Authors:  A Sancar; A M Hack; W D Rupp
Journal:  J Bacteriol       Date:  1979-01       Impact factor: 3.490

3.  Transient rates of synthesis of individual polypeptides in E. coli following temperature shifts.

Authors:  P G Lemaux; S L Herendeen; P L Bloch; F C Neidhardt
Journal:  Cell       Date:  1978-03       Impact factor: 41.582

4.  Identity of the B56.5 protein, the A-protein, and the groE gene product of Escherichia coli.

Authors:  F C Neidhardt; T A Phillips; R A VanBogelen; M W Smith; Y Georgalis; A R Subramanian
Journal:  J Bacteriol       Date:  1981-01       Impact factor: 3.490

5.  Structural and functional analysis of cloned DNA containing genes responsible for branched-chain amino acid transport in Escherichia coli.

Authors:  D L Oxender; J J Anderson; C J Daniels; R Landick; R P Gunsalus; G Zurawski; E Selker; C Yanofsky
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

6.  Selective synthesis of plasmid-coded proteins by Escherichia coli during recovery from chloramphenicol treatment.

Authors:  F C Neidhardt; R Wirth; M W Smith; R Van Bogelen
Journal:  J Bacteriol       Date:  1980-07       Impact factor: 3.490

7.  Positive regulatory gene for temperature-controlled proteins in Escherichia coli.

Authors:  F C Neidhardt; R A VanBogelen
Journal:  Biochem Biophys Res Commun       Date:  1981-05-29       Impact factor: 3.575

8.  Temperature-induced synthesis of specific proteins in Escherichia coli: evidence for transcriptional control.

Authors:  T Yamamori; T Yura
Journal:  J Bacteriol       Date:  1980-06       Impact factor: 3.490

9.  Genetic control of heat-shock protein synthesis and its bearing on growth and thermal resistance in Escherichia coli K-12.

Authors:  T Yamamori; T Yura
Journal:  Proc Natl Acad Sci U S A       Date:  1982-02       Impact factor: 11.205

10.  Structural interactions between amino acid residues at positions 22 and 211 in the tryptophan synthetase alpha chain of Escherichia coli.

Authors:  E J Murgola; C Yanofsky
Journal:  J Bacteriol       Date:  1974-02       Impact factor: 3.490

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  43 in total

1.  How a mutation in the gene encoding sigma 70 suppresses the defective heat shock response caused by a mutation in the gene encoding sigma 32.

Authors:  Y N Zhou; C A Gross
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

2.  Synergistic binding of DnaJ and DnaK chaperones to heat shock transcription factor σ32 ensures its characteristic high metabolic instability: implications for heat shock protein 70 (Hsp70)-Hsp40 mode of function.

Authors:  Hirotaka Suzuki; Ayami Ikeda; Sachie Tsuchimoto; Ko-ichi Adachi; Aki Noguchi; Yoshihiro Fukumori; Masaaki Kanemori
Journal:  J Biol Chem       Date:  2012-04-10       Impact factor: 5.157

Review 3.  Roles and regulation of the heat shock sigma factor sigma 32 in Escherichia coli.

Authors:  T Yura; Y Kawasaki; N Kusukawa; H Nagai; C Wada; R Yano
Journal:  Antonie Van Leeuwenhoek       Date:  1990-10       Impact factor: 2.271

4.  Heat shock response in Escherichia coli promotes assembly of plasmid encoded RNA polymerase beta-subunit into RNA polymerase.

Authors:  M V Kashlev; A I Gragerov; V G Nikiforov
Journal:  Mol Gen Genet       Date:  1989-04

5.  Suppression of the Escherichia coli rpoH opal mutation by ribosomes lacking S15 protein.

Authors:  R Yano; T Yura
Journal:  J Bacteriol       Date:  1989-03       Impact factor: 3.490

6.  Enhanced heterologous gene expression in novel rpoH mutants of Escherichia coli.

Authors:  M G Obukowicz; N R Staten; G G Krivi
Journal:  Appl Environ Microbiol       Date:  1992-05       Impact factor: 4.792

7.  Conserved region 2.1 of Escherichia coli heat shock transcription factor sigma32 is required for modulating both metabolic stability and transcriptional activity.

Authors:  Mina Horikoshi; Takashi Yura; Sachie Tsuchimoto; Yoshihiro Fukumori; Masaaki Kanemori
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

8.  Sensitization of Escherichia coli cells to oxidative stress by deletion of the rpoH gene, which encodes the heat shock sigma factor.

Authors:  T Kogoma; T Yura
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

9.  Independence of bacteriophage N15 lytic and linear plasmid replication from the heat shock proteins DnaJ, DnaK, and GrpE.

Authors:  K Tilly
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

10.  An analogue of the DnaJ molecular chaperone in Escherichia coli.

Authors:  C Ueguchi; M Kakeda; H Yamada; T Mizuno
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-01       Impact factor: 11.205

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