Literature DB >> 5326097

Phenomenon of transient repression in Escherichia coli.

K Paigen.   

Abstract

Paigen, Kenneth (Roswell Park Memorial Institute, Buffalo, N.Y.). Phenomenon of transient repression in Escherichia coli. J. Bacteriol. 91:1201-1209. 1966.-A family of mutants has been obtained in Escherichia coli K-12 in which beta-galactosidase is not inducible for approximately one cell generation after the cells are transferred to glucose from other carbon sources. After that period; the enzyme can be induced at the level appropriate to glucose-grown cultures of the parent cells. Among a wide variety of carbon sources, the only one capable of eliciting a state of transient repression is glucose. Conversely, transient repression occurs when cells are transferred to glucose from any of a variety of other carbon sources. The only exceptions to this so far discovered are lactose, gluconate, and xylose. Susceptibility to transient repression in mutants can also be induced in glucose-grown cells by a period of starvation. Mutant cells which have become susceptible to transient repression lose susceptibility in the presence of glucose only when they are under conditions which permit active protein synthesis. The presence of an inducer of beta-galactosidase is not required during this time, nor does pre-induction for beta-galactosidase diminish the susceptibility of mutants. At least two other catabolite repression-sensitive enzymes (galactokinase and tryptophanase) are also sensitive to transient repression, and the two phenomena are probably related. The absolute specificity of glucose and the pattern of response seen after growth in different carbon sources suggest that the endogenous metabolite which produces these repressions is far more readily derived from glucose in metabolism than it is from any other exogenous carbon source.

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Year:  1966        PMID: 5326097      PMCID: PMC316014          DOI: 10.1128/jb.91.3.1201-1209.1966

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


  11 in total

1.  SPECIFIC METABOLIC REPRESSION OF THREE INDUCED ENZYMES IN ESCHERICHIA COLI.

Authors:  E MCFALL; J MANDELSTAM
Journal:  Biochem J       Date:  1963-11       Impact factor: 3.857

2.  CHANGES IN THE INDUCIBILITY OF GALACTOKINASE AND BETA-GALACTOSIDASE DURING INHIBITION OF GROWTH IN ESCHERICHIA COLI.

Authors:  K PAIGEN
Journal:  Biochim Biophys Acta       Date:  1963-10-01

3.  Mutant of Aerobacter aerogenes lacking glucose repression.

Authors:  F C NEIDHARDT
Journal:  J Bacteriol       Date:  1960-10       Impact factor: 3.490

4.  The initial kinetics of enzyme induction.

Authors:  A B PARDEE; L S PRESTIDGE
Journal:  Biochim Biophys Acta       Date:  1961-04-29

5.  Reversal of the glucose inhibition of histidase biosynthesis in Aerobacter aerogenes.

Authors:  F C NEIDHARDT; B MAGASANIK
Journal:  J Bacteriol       Date:  1957-02       Impact factor: 3.490

6.  Inhibitory effect of glucose on enzyme formation.

Authors:  B MAGASANIK; F C NEIDHARDT
Journal:  Nature       Date:  1956-10-13       Impact factor: 49.962

7.  FACTORS INFLUENCING THE ENZYMIC ACTIVITIES OF BACTERIA.

Authors:  E F Gale
Journal:  Bacteriol Rev       Date:  1943-09

8.  The influence of the presence of glucose during growth on the enzymic activities of Escherichia coli: comparison of the effect with that produced by fermentation acids.

Authors:  H M Epps; E F Gale
Journal:  Biochem J       Date:  1942-09       Impact factor: 3.857

9.  The repression of constitutive beta-galactosidase in Escherichia coli by glucose and other carbon sources.

Authors:  J MANDELSTAM
Journal:  Biochem J       Date:  1962-03       Impact factor: 3.857

10.  Catabolite repression.

Authors:  B MAGASANIK
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1961
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  24 in total

1.  Transient repression of catabolite-sensitive enzyme synthesis elicited by 2,4-dinitrophenol.

Authors:  R Oki
Journal:  J Bacteriol       Date:  1975-09       Impact factor: 3.490

2.  Two types of glucose effects on beta-galactosidase synthesis in a membrane fraction of Escherichia coli: correlation with repression observed in intact cells.

Authors:  H Seto; Y Nagata; B Maruo
Journal:  J Bacteriol       Date:  1975-05       Impact factor: 3.490

3.  Discriminating tastes: physiological contributions of the Hfq-binding small RNA Spot 42 to catabolite repression.

Authors:  Chase L Beisel; Gisela Storz
Journal:  RNA Biol       Date:  2011-07-26       Impact factor: 4.652

4.  Regulation of lac operon expression: reappraisal of the theory of catabolite repression.

Authors:  B L Wanner; R Kodaira; F C Neidhardt
Journal:  J Bacteriol       Date:  1978-12       Impact factor: 3.490

5.  The influence of recent growth history on the phenotype of Escherichia coli.

Authors:  V Moses; P B Sharp
Journal:  Folia Microbiol (Praha)       Date:  1972       Impact factor: 2.099

6.  Induction and repression of L-arabinose isomerase in Salmonella typhimurium.

Authors:  A K Bhattacharya; M Chakravorty
Journal:  J Bacteriol       Date:  1971-04       Impact factor: 3.490

7.  Physiological basis of transient repression of catabolic enzymes in Escherichia coli.

Authors:  B Tyler; B Magasanik
Journal:  J Bacteriol       Date:  1970-05       Impact factor: 3.490

8.  Molecular basis of transient repression of beta-galactosidase in Escherichia coli.

Authors:  B Tyler; B Magasanik
Journal:  J Bacteriol       Date:  1969-02       Impact factor: 3.490

9.  Paradoxical effect of weak inducers on the lac operon of Escherichia coli.

Authors:  B Williams; K Paigen
Journal:  J Bacteriol       Date:  1968-11       Impact factor: 3.490

10.  Catabolite translational effects on the lac messenger RNA of Escherichia coli K12.

Authors:  C Sanchez de Rivas; B S Méndez
Journal:  Mol Gen Genet       Date:  1976-10-18
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