Literature DB >> 323228

Physiological regulation of a decontrolled lac operon.

B L Wanner, R Kodaira, F C Neidhardt.   

Abstract

The expression of the lac operon was studied under a variety of growth conditions in induced and in constitutive cells of Escherichia coli that carried different catabolite-insensitive lac promoters. Use of such "decontrolled" lac operons permitted a study of the expression of an operon that was presumably subject only to passive control. Since the use of toluenized cells was demonstrated not to be completely reliable, all enzyme assays were performed on sonic supernatant fluids. The cells contained different catabolite-insensitive promoters, which included the L1 and UV5 lac promoters, as well as others isolated in this study. There were three major observations. First, small but real carbon source effects were seen. Second, there was only a small change in beta-galactosidase specific activity with changes in the growth rate. This result implies a limited transcription and/or translation capacity within the cell. Third, at rapid growth rates, most promoters exhibited a decreased expression. The UV5 promoter, which was the "strongest" promoter, was an exception. A mechanism to explain this promoter-dependent control is discussed.

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Year:  1977        PMID: 323228      PMCID: PMC235196          DOI: 10.1128/jb.130.1.212-222.1977

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


  24 in total

1.  Activation of transcription by guanosine 5'-diphosphate,3'-diphosphate, transfer ribonucleic acid, and novel protein from Escherichia coli.

Authors:  M Aboud; I Pastan
Journal:  J Biol Chem       Date:  1975-03-25       Impact factor: 5.157

Review 2.  Recalibrated linkage map of Escherichia coli K-12.

Authors:  B J Bachmann; K B Low; A L Taylor
Journal:  Bacteriol Rev       Date:  1976-03

3.  Inapparent correlation between guanosine tetraphosphate levels and RNA contents in Escherichia coli.

Authors:  S R Khan; H Yamazaki
Journal:  Biochem Biophys Res Commun       Date:  1974-07-10       Impact factor: 3.575

4.  Culture medium for enterobacteria.

Authors:  F C Neidhardt; P L Bloch; D F Smith
Journal:  J Bacteriol       Date:  1974-09       Impact factor: 3.490

5.  Macromolecular composition during steady-state growth of Escherichia coli B-r.

Authors:  P P Dennis; H Bremer
Journal:  J Bacteriol       Date:  1974-07       Impact factor: 3.490

6.  Intracistronic polarity during dissociation of translation from transcription in Escherichia coli.

Authors:  M T Hansen; P M Bennett; K von Meyenburg
Journal:  J Mol Biol       Date:  1973-07-15       Impact factor: 5.469

7.  Evidence for two sites in the lac promoter region.

Authors:  J Beckwith; T Grodzicker; R Arditti
Journal:  J Mol Biol       Date:  1972-08-14       Impact factor: 5.469

8.  Mechanism of initiation and repression of in vitro transcription of the lac operon of Escherichia coli.

Authors:  L Eron; R Block
Journal:  Proc Natl Acad Sci U S A       Date:  1971-08       Impact factor: 11.205

9.  Effects of guanosine tetraphosphate, guanosine pentaphosphate, and beta-gamma methylenyl-guanosine pentaphosphate on gene expression of Escherichia coli in vitro.

Authors:  H L Yang; G Zubay; E Urm; G Heiness; M Cashel
Journal:  Proc Natl Acad Sci U S A       Date:  1974-01       Impact factor: 11.205

10.  Adenosine triphosphate-linked control of Pseudomonas aeruginosa glucose-6-phosphate dehydrogenase.

Authors:  T Lessie; F C Neidhardt
Journal:  J Bacteriol       Date:  1967-04       Impact factor: 3.490

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  84 in total

1.  CspA, CspB, and CspG, major cold shock proteins of Escherichia coli, are induced at low temperature under conditions that completely block protein synthesis.

Authors:  J P Etchegaray; M Inouye
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

2.  DNA gyrase, CS7.4, and the cold shock response in Escherichia coli.

Authors:  P G Jones; R Krah; S R Tafuri; A P Wolffe
Journal:  J Bacteriol       Date:  1992-09       Impact factor: 3.490

3.  Levels of major proteins of Escherichia coli during growth at different temperatures.

Authors:  S L Herendeen; R A VanBogelen; F C Neidhardt
Journal:  J Bacteriol       Date:  1979-07       Impact factor: 3.490

4.  Growth-rate-dependent expression and cloning of gnd alleles from natural isolates of Escherichia coli.

Authors:  G J Barcak; R E Wolf
Journal:  J Bacteriol       Date:  1988-01       Impact factor: 3.490

5.  Loss of 4.5S RNA induces the heat shock response and lambda prophage in Escherichia coli.

Authors:  D B Bourgaize; T A Phillips; R A VanBogelen; P G Jones; F C Neidhardt; M J Fournier
Journal:  J Bacteriol       Date:  1990-02       Impact factor: 3.490

6.  Identification of a novel regulatory protein (CsrD) that targets the global regulatory RNAs CsrB and CsrC for degradation by RNase E.

Authors:  Kazushi Suzuki; Paul Babitzke; Sidney R Kushner; Tony Romeo
Journal:  Genes Dev       Date:  2006-09-15       Impact factor: 11.361

7.  Growth-rate-dependent partitioning of RNA polymerases in bacteria.

Authors:  Stefan Klumpp; Terence Hwa
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-10       Impact factor: 11.205

Review 8.  The leucine-responsive regulatory protein, a global regulator of metabolism in Escherichia coli.

Authors:  J M Calvo; R G Matthews
Journal:  Microbiol Rev       Date:  1994-09

9.  Vibrio natriegens as a fast-growing host for molecular biology.

Authors:  Matthew T Weinstock; Eric D Hesek; Christopher M Wilson; Daniel G Gibson
Journal:  Nat Methods       Date:  2016-08-29       Impact factor: 28.547

10.  Expression of genes kdsA and kdsB involved in 3-deoxy-D-manno-octulosonic acid metabolism and biosynthesis of enterobacterial lipopolysaccharide is growth phase regulated primarily at the transcriptional level in Escherichia coli K-12.

Authors:  H Strohmaier; P Remler; W Renner; G Högenauer
Journal:  J Bacteriol       Date:  1995-08       Impact factor: 3.490

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