Literature DB >> 1091620

Stimulation of adenosine 5'-triphosphate-dependent in vitro deoxyribonucleic acid replication by factors from the periplasmic space of Escherichia coli.

D W Smith, P Boerner.   

Abstract

In vitro deoxyribonucleic acid (DNA) synthesis systems based on an earlier system using pencillin have been developed which use osmotic lysis of lysozyme-formed spheroplasts of Escherichia coli cells embedded in an agarose matrix. An adenosine 5'-triphosphate (ATP)-dependent semiconservative mode, or replicative mode, of in vitro DNA synthesis is exhibited which is sensitivie to nalidixic acid. These systems require growth of the agar-embedded cells in a preincubation medium before spheroplast formation and osmotic lysis. Inhibitor studies suggest that one or more required macromolecular species are synthesized during this preincubation growth period. Osmotic shock fluid from E. coli contains macromolecular factors which preferentially stimulate the ATP- dependent semiconservative mode of in vitro DNA synthesis. In some cases, the ATP independent mode of synthesis is inhibited by shock fluid. Evidence is presented that the stimulating factors found in the osmotic shock fluid come from the E. coli periplasmic space. This stimulation is observed using either toluene-treated cells or lysed agar-embedded ethylene glycol-bis-(beta-aminoethyl ether) N,N'-tetraacetate-lysozyme spheroplasts, and is thus independent of the in vitro DNA synthesis system used. Shock fluid obtained from a given E. coli dna mutant does not stimulate in vitro DNA synthesis by that mutant. However, in some cases, shock fluid from one class of dna mutants does stimulate ATP dependent in vitro DNA synthesis by another class of dna mutants, in a thermosensitive reacaction. Gently prepared cell extracts also stimulate ATP-dependent in vitro DNA synthesis, whereas cell extracts prepared by more severe procedures inhibit this in vitro synthesis. Severl stimulating DNA replication factors may be present in the osmotic shock fluid, including products of E. coli dna genes.

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Year:  1975        PMID: 1091620      PMCID: PMC235653          DOI: 10.1128/jb.122.1.159-170.1975

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


  35 in total

1.  IMPROVED METHOD FOR THE ISOLATION OF THYMINE-REQUIRING MUTANTS OF ESCHERICHIA COLI.

Authors:  K A STACEY; E SIMSON
Journal:  J Bacteriol       Date:  1965-08       Impact factor: 3.490

2.  A fine-structure genetic and chemical study of the enzyme alkaline phosphatase of E. coli. I. Purification and characterization of alkaline phosphatase.

Authors:  A GAREN; C LEVINTHAL
Journal:  Biochim Biophys Acta       Date:  1960-03-11

3.  BACTERIAL PROTOPLASTS INDUCED BY PENICILLIN.

Authors:  J Lederberg
Journal:  Proc Natl Acad Sci U S A       Date:  1956-09       Impact factor: 11.205

4.  Initiation of DNA synthesis: synthesis of phiX174 replicative form requires RNA synthesis resistant to rifampicin.

Authors:  R Schekman; W Wickner; O Westergaard; D Brutlag; K Geider; L L Bertsch; A Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  1972-09       Impact factor: 11.205

5.  Mechanism of assembly of the outer membrane of Salmonella typhimurium. Isolation and characterization of cytoplasmic and outer membrane.

Authors:  M J Osborn; J E Gander; E Parisi; J Carson
Journal:  J Biol Chem       Date:  1972-06-25       Impact factor: 5.157

6.  Isolation of an E. coli strain with a mutation affecting DNA polymerase.

Authors:  P De Lucia; J Cairns
Journal:  Nature       Date:  1969-12-20       Impact factor: 49.962

7.  DNA synthesis in vitro.

Authors:  D W Smith; H E Schaller; F J Bonhoeffer
Journal:  Nature       Date:  1970-05-23       Impact factor: 49.962

8.  Interaction of rifamycin with bacterial RNA polymerase.

Authors:  W Wehrli; F Knüsel; K Schmid; M Staehelin
Journal:  Proc Natl Acad Sci U S A       Date:  1968-10       Impact factor: 11.205

9.  Replication and repair of DNA in cells of Escherichia coli treated with toluene.

Authors:  R E Moses; C C Richardson
Journal:  Proc Natl Acad Sci U S A       Date:  1970-10       Impact factor: 11.205

10.  Solubilization of the cytoplasmic membrane of Escherichia coli by Triton X-100.

Authors:  C A Schnaitman
Journal:  J Bacteriol       Date:  1971-10       Impact factor: 3.490

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