Literature DB >> 4382255

Pool sizes of metabolic intermediates and their relation to glucose repression of beta-galactosidase synthesis in Escherichia coli.

C Prevost, V Moses.   

Abstract

1. The intermediary metabolism of two strains of Escherichia coli has been examined. One strain (Q22) exhibits acute transient repression of beta-galactosidase synthesis when glucose is supplied to cells growing on glycerol; the other strain (W3110) does not. The two strains do not differ genetically in their lac operons. 2. Strain Q22 uses about twice as much glucose as strain W3110 per unit of cell mass produced. 3. Pentose phosphate-cycle activity in the presence of glucose is much stronger in strain Q22 than in strain W3110. 4. In strain Q22 the pool sizes of glucose 6-phosphate, 6-phosphogluconate, fructose 1,6-diphosphate and NADPH increase when glucose is added to cells growing on glycerol, and beta-galactosidase synthesis is severely inhibited. After about 1hr. the synthesis of beta-galactosidase is partly resumed, and the pool sizes of the four compounds fall. ATP, NADH and several other phosphorylated compounds show no concentration changes. 5. These concentration changes do not occur in strain W3110, in which beta-galactosidase synthesis is only rather weakly repressed by glucose. 6. It is suggested that repression of enzyme synthesis by glucose requires the rapid operation of the pentose phosphate cycle, and is mediated by one of the four substances whose concentration rises and later falls in strain Q22. A definite choice of effector from among these four possibilities cannot at present be made.

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Year:  1967        PMID: 4382255      PMCID: PMC1270415          DOI: 10.1042/bj1030349

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  26 in total

1.  Carbohydrate oxidation by Pseudomonas fluorescens. I. The mechanism of glucose and gluconate oxidation.

Authors:  W A WOOD; R F SCHWERDT
Journal:  J Biol Chem       Date:  1953-04       Impact factor: 5.157

2.  Isolation and purification of radioactive sugars by means of paper chromatography.

Authors:  W E PUTMAN; W Z HASSID
Journal:  J Biol Chem       Date:  1952-05       Impact factor: 5.157

3.  Measurement of the activity of the hexose monophosphate pathway of glucose metabolism with the use of [18O]glucose. Variations in its activity in Escherichia coli with growth conditions.

Authors:  P Model; D Rittenberg
Journal:  Biochemistry       Date:  1967-01       Impact factor: 3.162

4.  Genetic control of catabolite repression of the lac operon in Escherichia coli.

Authors:  W F Loomis; B Magasanik
Journal:  Biochem Biophys Res Commun       Date:  1965-07-12       Impact factor: 3.575

5.  Phenomenon of transient repression in Escherichia coli.

Authors:  K Paigen
Journal:  J Bacteriol       Date:  1966-03       Impact factor: 3.490

6.  The study of metabolic compartmentalization.

Authors:  V Moses; K K Lonberg-Holm
Journal:  J Theor Biol       Date:  1966-02       Impact factor: 2.691

7.  Involvement of the lac regulatory genes in catabolite repression in Escherichia coli.

Authors:  J Palmer; V Moses
Journal:  Biochem J       Date:  1967-05       Impact factor: 3.857

8.  Nature of the effector of catabolite repression of beta-galactosidase in Escherichia coli.

Authors:  W F Loomis; B Magasanik
Journal:  J Bacteriol       Date:  1966-07       Impact factor: 3.490

9.  Altered end-product patterns and catabolite repression in Escherichia coli.

Authors:  W J Dobrogosz
Journal:  J Bacteriol       Date:  1966-06       Impact factor: 3.490

10.  Catabolite repression of beta-galactosidase synthesis in Escherichia coli.

Authors:  V Moses; C Prevost
Journal:  Biochem J       Date:  1966-08       Impact factor: 3.857

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  21 in total

1.  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

2.  Biosynthesis and regulation of fructose-1,6-bisphosphatase and phosphofructokinase in Saccharomyces cerevisiae grown in the presence of glucose and gluconeogenic carbon sources.

Authors:  J J Foy; J K Bhattacharjee
Journal:  J Bacteriol       Date:  1978-11       Impact factor: 3.490

3.  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

Review 4.  Allosteric controls of amphilbolic pathways in bacteria.

Authors:  B D Sanwal
Journal:  Bacteriol Rev       Date:  1970-03

5.  Factors affecting the regulation of staphylococcal enterotoxin B.

Authors:  S A Morse; J N Baldwin
Journal:  Infect Immun       Date:  1973-06       Impact factor: 3.441

6.  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

7.  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

8.  Transient repression of the lac operon.

Authors:  B Tyler; W F Loomis; B Magasanik
Journal:  J Bacteriol       Date:  1967-12       Impact factor: 3.490

9.  Effect of amino sugars on catabolite repression in Escherichia coli.

Authors:  W J Dobrogosz
Journal:  J Bacteriol       Date:  1968-02       Impact factor: 3.490

10.  Involvement of the lac regulatory genes in catabolite repression in Escherichia coli.

Authors:  J Palmer; V Moses
Journal:  Biochem J       Date:  1967-05       Impact factor: 3.857

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