Literature DB >> 4167433

The regulatory process in the de-repression of enzyme synthesis. Alkaline phosphatase of Bacillus subtilis.

V Moses.   

Abstract

1. The kinetics of de-repression of alkaline phosphatase in Bacillus subtilis were studied after the removal of P(i). Enzyme activity appeared about 10min. after removal of P(i), whereas ;enzyme-forming potential' appeared after 6min. 2. Protein synthesis is not impaired for at least 20min. on removal of P(i), but RNA synthesis is considerably diminished. 3. Adding chloramphenicol to cells without P(i), just at the time they start to make enzyme-forming potential, does not affect the differential rate of enzyme synthesis compared with total protein. Enzyme-forming potential accumulates to about normal levels in the presence of chloramphenicol, even though peptide-bond formation is inhibited by more than 95%. 4. Similar experiments performed with actinomycin C show more complex effects. Actinomycin initially prevents RNA synthesis and also the synthesis of enzyme-forming potential. After some minutes RNA synthesis resumes at a low rate, to be followed 4min. later by enzyme synthesis. Enzyme-forming potential can accumulate in the presence of actinomycin after the resumption of RNA synthesis. Protein synthesis, initially inhibited by actinomycin as a consequence of the effect on RNA synthesis, is later directly inhibited by actinomycin. 5. Adding actinomycin to de-repressed cells already making enzyme stops enzyme synthesis within 4-5min. Enzyme synthesis resumes, as before, 4min. after the resumption of RNA synthesis. 6. Adding P(i) together with actinomycin to de-repressed cells synthesizing enzyme does not result in a lower yield of enzyme compared with actinomycin alone. 7. Actinomycin is less effective an inhibitor of RNA and protein synthesis in P(i)-starved cells if P(i) is also added. 8. These results are discussed in view of the three main models for the regulation of enzyme induction: regulation at the level of transcription only, at translation only, or a coupled model in which transcription requires concomitant translation. It is concluded that the present evidence most powerfully supports the model of transcriptional regulation.

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Year:  1967        PMID: 4167433      PMCID: PMC1270464          DOI: 10.1042/bj1030650

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


  16 in total

1.  Genetic regulatory mechanisms in the synthesis of proteins.

Authors:  F JACOB; J MONOD
Journal:  J Mol Biol       Date:  1961-06       Impact factor: 5.469

2.  Thymine starvation and enzyme synthesis.

Authors:  E MCFALL; B MAGASANIK
Journal:  Biochim Biophys Acta       Date:  1960-12-18

3.  Studies on a mutant of Escherichia coli with unbalanced ribonucleic acid synthesis. II. The concomitance of ribonucleic acid synthesis with resumed protein synthesis.

Authors:  E BOREK; A RYAN
Journal:  J Bacteriol       Date:  1958-01       Impact factor: 3.490

4.  Messenger RNA turnover and protein synthesis in B. subtilis inhibited by actinomycin D.

Authors:  C LEVINTHAL; A KEYNAN; A HIGA
Journal:  Proc Natl Acad Sci U S A       Date:  1962-09-15       Impact factor: 11.205

Review 5.  Genetic transcription.

Authors:  G S Stent
Journal:  Proc R Soc Lond B Biol Sci       Date:  1966-03-22

6.  Effect of actinomycin on the synthesis of macromolecules in Escherichia coli.

Authors:  V Moses; P B Sharp
Journal:  Biochim Biophys Acta       Date:  1966-04-18

7.  Regulation of enzyme synthesis in an enucleate cell.

Authors:  T Spencer; H Harris
Journal:  Biochem J       Date:  1964-05       Impact factor: 3.857

8.  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

9.  Lifetime of bacterial messenger ribonucleic acid.

Authors:  V Moses; M Calvin
Journal:  J Bacteriol       Date:  1965-11       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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  4 in total

1.  Regulation of the formation of alkaline phosphatase during neomycin biosynthesis.

Authors:  S K Bandyopadhyay; S K Majumdar
Journal:  Antimicrob Agents Chemother       Date:  1974-04       Impact factor: 5.191

2.  Sporulation in Bacillus subtilis 168. Comparison of alkaline phosphatase from sporulating and vegetative cells.

Authors:  A R Glenn; J Mandelstam
Journal:  Biochem J       Date:  1971-06       Impact factor: 3.857

3.  Extracellular phosphatases of Chlamydomonas reinhardi and their regulation.

Authors:  N J Patni; S W Dhawale; S Aaronson
Journal:  J Bacteriol       Date:  1977-04       Impact factor: 3.490

4.  Relationship between alkaline phosphatase and neomycin formation in Streptomyces fradiae.

Authors:  M K Majumdar; S K Majumdar
Journal:  Biochem J       Date:  1971-05       Impact factor: 3.857

  4 in total

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