Literature DB >> 374996

Rifampicin supersensitivity of rho strains of E. coli, and suppression by sur mutation.

S K Guterman, C L Howitt.   

Abstract

Escherichia coli strains with mutations rho-115, rho-ts15, rho-101 (psu-1) or rho-102 (psu-2) are more sensitive ("supersensitive") to rifampicin than isogenic parent strains, as measured by growth rate in broth and colony forming efficiency on solid media with 5, 10, or 20 microgram of rifampicin per ml. There is no change in sensitivity of rho mutants to the antibiotics penicillin, erythromycin, chloramphenicol, or the detergent desoxycholate. The rho-101 or rho-102 mutations confer rifampicin supersensitivity at 32 degrees C but not 42 degrees C. Mutants of a rho-115 strain that have lost polarity suppression can be isolated by selection for rifampicin resistance. This phenotype, Sur, is not due to reversion of the original rho gene mutation but to a second mutation perhaps in the gene for rho protein or the gene for the beta subunit of RNA polymerase. One class of Sur mutation, occurring in rho-115 cells isolated as resistant to 20 microgram of rifampicin per ml, is co-transducible with the marker ilv, and the gene order is rbs-ilv-sur-38. A model suggested by this map position is that the mutations rho-115 and sur-38 define the domain of rho protein which interacts with the beta subunit of RNA polymerase.

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Year:  1979        PMID: 374996     DOI: 10.1007/bf00267541

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


  30 in total

1.  New features of the regulation of the tryptophan operon.

Authors:  K Bertrand; L Korn; F Lee; T Platt; C L Squires; C Squires; C Yanofsky
Journal:  Science       Date:  1975-07-04       Impact factor: 47.728

2.  Reconstitution of bacterial DNA-dependent RNA-polymerase from isolated subunits as a tool for the elucidation of the role of the subunits in transcription.

Authors:  A Heil; W Zillig
Journal:  FEBS Lett       Date:  1970-12       Impact factor: 4.124

3.  Suppression of polarity of insertion mutations in the gal operon and N mutations in bacteriophage lambda.

Authors:  O Reyes; M Gottesman; S Adhya
Journal:  J Bacteriol       Date:  1976-06       Impact factor: 3.490

4.  Polar mutations in lac, gal and phage lambda consist of a few IS-DNA sequences inserted with either orientation.

Authors:  M Fiandt; W Szybalski; M H Malamy
Journal:  Mol Gen Genet       Date:  1972

5.  Transcription of the early region of bacteriophage T7: selective initiation with dinucleotides.

Authors:  E G Minkley; D Pribnow
Journal:  J Mol Biol       Date:  1973-06-25       Impact factor: 5.469

6.  Termination factor for RNA synthesis.

Authors:  J W Roberts
Journal:  Nature       Date:  1969-12-20       Impact factor: 49.962

7.  Frameshift mutations in the lactose operon of E. coli.

Authors:  M H Malamy
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1966

8.  Induction of sigma factor synthesis in Escherichia coli by the N gene product of bacteriophage lambda.

Authors:  Y Nakamura; T Yura
Journal:  Proc Natl Acad Sci U S A       Date:  1976-12       Impact factor: 11.205

9.  An RNA-dependent nucleoside triphosphate phosphohydrolase (ATPase) associated with rho termination factor.

Authors:  C Lowery-Goldhammer; J P Richardson
Journal:  Proc Natl Acad Sci U S A       Date:  1974-05       Impact factor: 11.205

10.  ATPase activity required for termination of transcription by the Escherichia coli protein factor rho.

Authors:  B H Howard; B de Crombrugghe
Journal:  J Biol Chem       Date:  1976-04-25       Impact factor: 5.157

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  27 in total

1.  Cloning and nucleotide sequence of the firA gene and the firA200(Ts) allele from Escherichia coli.

Authors:  I B Dicker; S Seetharam
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

2.  Regulation of DNA superhelicity by rpoB mutations that suppress defective Rho-mediated transcription termination in Escherichia coli.

Authors:  G F Arnold; I Tessman
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

Review 3.  Mastering the control of the Rho transcription factor for biotechnological applications.

Authors:  Tomás G Villa; Ana G Abril; Angeles Sánchez-Pérez
Journal:  Appl Microbiol Biotechnol       Date:  2021-05-08       Impact factor: 4.813

4.  Reduced superhelicity of plasmid DNA produced by the rho-15 mutation in Escherichia coli.

Authors:  J S Fassler; G F Arnold; I Tessman
Journal:  Mol Gen Genet       Date:  1986-09

5.  Rho and NusG suppress pervasive antisense transcription in Escherichia coli.

Authors:  Jason M Peters; Rachel A Mooney; Jeffrey A Grass; Erik D Jessen; Frances Tran; Robert Landick
Journal:  Genes Dev       Date:  2012-12-01       Impact factor: 11.361

6.  Incompatibility of Escherichia coli rho mutants with plasmids is mediated by plasmid-specific transcription.

Authors:  T K Li; Y A Panchenko; M Drolet; L F Liu
Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

7.  Escherichia coli Rho factor is involved in lysis of bacteriophage T4-infected cells.

Authors:  C H Linder; K Carlson
Journal:  Genetics       Date:  1985-10       Impact factor: 4.562

8.  A mutant rho ATPase from Escherichia coli that is temperature-sensitive in the presence of RNA.

Authors:  R B Kent; S K Guterman
Journal:  Mol Gen Genet       Date:  1981

9.  Pyrophosphate inhibition of rho ATPase: a mechanism of coupling to RNA polymerase activity.

Authors:  R B Kent; S K Guterman
Journal:  Proc Natl Acad Sci U S A       Date:  1982-07       Impact factor: 11.205

10.  A novel rho promoter::Tn10 mutation suppresses and ftsQ1(Ts) missense mutation in an essential Escherichia coli cell division gene by a mechanism not involving polarity suppression.

Authors:  D R Storts; A Markovitz
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

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