Literature DB >> 4580555

Derepression of uridine diphosphate-glucose pyrophosphorylase (galU) in capR(lon), capS, and capT mutants and studies on the galU repressor.

C E Buchanan, A Markovitz.   

Abstract

Mutation of the capR(lon), capS, or capT genes in Escherichia coli K-12 causes overproduction of capsular polysaccharide leading to a mucoid phenotype. Several of the enzymes involved in capsular polysaccharide synthesis are derepressed in cap mutants. Previously it was shown that uridine diphosphate-glucose (UDPG) pyrophosphorylase, an enzyme involved in the synthesis of three of the nucleotide sugar precursors of the capsule, is derepressed in capR mutants. The control of galU, the gene which codes for UDPG pyrophosphorylase, is described in this study. In addition, it has been found that the enzyme is also derepressed in capS and capT mutants. The effect of galU gene dosage in cap mutants and the wild-type strain (all lysogenic for phi80) was studied by infecting them with the purified transducing phage phi80dgalU. The level of UDPG pyrophosphorylase increased in proportion to the number of galU copies added. The rate of enzyme synthesis in the mutants was about sixfold higher than in the wild type per galU gene added for multiplicities of infection from one to twenty. Thus, all the galU copies added to the wild-type lysogen were repressed. We obtain greater than 20 galU copies per cell by infecting the nonlysogenic strain which allows multiplication of phi80dgalU. With some number of galU copies greater than 20, the rate of UDPG pyrophosphorylase synthesis in the wild type approaches the mutant rate of synthesis. The results suggest that there may indeed be a galU repressor pool in the cell which can be completely titrated. This pool must be composed of more than 20 galU repressor molecules. Since the capR, capS, and capT gene products or combinations thereof are known to control other widely separated operons of the cell besides the galU gene, it is postulated that the galU repressor may be capable of binding other operators. This would account for the relatively large pool of galU repressors per cell.

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Year:  1973        PMID: 4580555      PMCID: PMC246349          DOI: 10.1128/jb.115.3.1011-1020.1973

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


  58 in total

1.  The feedback inhibition of thymidine kinase.

Authors:  T R BREITMAN
Journal:  Biochim Biophys Acta       Date:  1963-01-08

2.  Some aspects of regulation in the synthesis of the enzymes governing galactose metabolism.

Authors:  G BUTTIN
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1961

3.  Biosynthesis of beta-D-galactosidase controlled by phage-carried genes. III. Dereprssion of beta-d-galactosidase synthesis following induction of phage development in lysogenic bacteria.

Authors:  H R REVEL; S E LURIA; N L YOUNG
Journal:  Proc Natl Acad Sci U S A       Date:  1961-12-15       Impact factor: 11.205

4.  Bacterial cell division regulation: lysogenization of conditional cell division lon - mutants of Escherichia coli by bacteriophage.

Authors:  J R Walker; C L Ussery; J S Allen
Journal:  J Bacteriol       Date:  1973-03       Impact factor: 3.490

5.  DNA-dependent in vitro synthesis of enzymes of the galactose operon of Escherichia coli.

Authors:  W Wetekam; K Staack; R Ehring
Journal:  Mol Gen Genet       Date:  1971

6.  Nucleotide distribution and functional orientation in the deoxyribonucleic acid of phage phi 80.

Authors:  A Skalka
Journal:  J Virol       Date:  1969-02       Impact factor: 5.103

7.  Prophage repression as a model for the study of gene regulation. I. Titration of the lambda repressor.

Authors:  H Wiesmeyer
Journal:  J Bacteriol       Date:  1966-01       Impact factor: 3.490

8.  Specific binding of the lambda phage repressor to lambda DNA.

Authors:  M Ptashne
Journal:  Nature       Date:  1967-04-15       Impact factor: 49.962

9.  Derepression of phosphomannose isomerase by regulator gene mutations involved in capsular polysaccharide synthesis in Escherichia coli K-12.

Authors:  A Markovitz; M M Lieberman; N Rosenbaum
Journal:  J Bacteriol       Date:  1967-11       Impact factor: 3.490

10.  Multiple regulator gene control of the galactose operon in Escherichia coli K-12.

Authors:  S S Hua; A Markovitz
Journal:  J Bacteriol       Date:  1972-06       Impact factor: 3.490

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  3 in total

1.  Regulation of galactose operon at the gal operator-promoter region in Escherichia coli K-12.

Authors:  S S Hua; A Markovitz
Journal:  J Bacteriol       Date:  1975-05       Impact factor: 3.490

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.  Multiple regulation of the galactose operon-genetic evidence for a distinct site in the galactose operon that responds to capR gene regulation in Escherichia coli K-12.

Authors:  S S Hua; A Markovitz
Journal:  Proc Natl Acad Sci U S A       Date:  1974-02       Impact factor: 11.205

  3 in total

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