Literature DB >> 6389508

Phase separation between nucleoid and cytoplasm in Escherichia coli as defined by immersive refractometry.

J A Valkenburg, C L Woldringh.   

Abstract

The refractive indices of nucleoid and cytoplasm in Escherichia coli were derived theoretically and experimentally. For the theoretical estimates, we made use of the known macromolecular composition of E. coli B/r (G. Churchward and H. Bremer, J. Theor. Biol. 94:651-670, 1982) and of estimates of cell and nucleoid volumes. These were obtained from micrographs of living bacteria made with a confocal scanning light microscope. The theoretical values were calculated, assuming that all DNA occurred in the nucleoid and that all protein and RNA occurred in the cytoplasm. Comparison with experimental refractive index values directly obtained by immersive refractometry showed that, besides its DNA, the nucleoid must contain an additional amount of solids equivalent to 8.6% (wt/vol) protein. With the nucleoid containing 6.8% (wt/vol) DNA and 8.6% (wt/vol) protein and the cytoplasm containing 21% (wt/vol) protein and 4% (wt/vol) RNA, a mass difference is obtained, which accounts for the phase separation observed between the nucleoid and cytoplasm in living cells by phase-contrast microscopy. The decrease in the refractive index of the nucleoid relative to that of the cytoplasm observed upon, for instance, OsO4 fixation was interpreted as being indicative of the loss of protein content in the nucleoid.

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Year:  1984        PMID: 6389508      PMCID: PMC215833          DOI: 10.1128/jb.160.3.1151-1157.1984

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


  24 in total

1.  Morphological analysis of nuclear separation and cell division during the life cycle of Escherichia coli.

Authors:  C L Woldringh
Journal:  J Bacteriol       Date:  1976-01       Impact factor: 3.490

2.  Size and DNA content of purfied E. coli nucleoids observed by fluorencence microscopy.

Authors:  R M Hecht; R T Taggart; D E Pettijohn
Journal:  Nature       Date:  1975-01-03       Impact factor: 49.962

3.  Growth, cell and nuclear divisions in some bacteria.

Authors:  M SCHAECHTER; J P WILLIAMSON; J R HOOD; A L KOCH
Journal:  J Gen Microbiol       Date:  1962-11

4.  The Biology of Isolated Chromatin: Chromosomes, biologically active in the test tube, provide a powerful tool for the study of gene action.

Authors:  J Bonner; M E Dahmus; D Fambrough; R C Huang; K Marushige; D Y Tuan
Journal:  Science       Date:  1968-01-05       Impact factor: 47.728

Review 5.  Contact-site cross-linking agents.

Authors:  G R Kunkel; M Mehrabian; H G Martinson
Journal:  Mol Cell Biochem       Date:  1981-01-20       Impact factor: 3.396

6.  Macromolecular composition of bacteria.

Authors:  G Churchward; H Bremer; R Young
Journal:  J Theor Biol       Date:  1982-02-07       Impact factor: 2.691

7.  Electron microscopy of frozen-hydrated bacteria.

Authors:  J Dubochet; A W McDowall; B Menge; E N Schmid; K G Lickfeld
Journal:  J Bacteriol       Date:  1983-07       Impact factor: 3.490

8.  In vitro studies of the fixation of DNA, nucleoprotamine, nucleohistone and proteins.

Authors:  E Kellenberger; E Carlemalm; E Stauffer; C Kellenberger; H Wunderli
Journal:  Eur J Cell Biol       Date:  1981-08       Impact factor: 4.492

9.  The interpretation of chemically fixed and freeze-fractured bacterial nucleoplasm.

Authors:  N Nanninga; C L Woldringh
Journal:  Acta Histochem Suppl       Date:  1981

10.  Visualization of the nucleoid in living bacteria on poly-lysine coated surfaces by the immersion technique.

Authors:  J S Binnerts; C L Woldringh; G J Brakenhoff
Journal:  J Microsc       Date:  1982-03       Impact factor: 1.758

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  31 in total

Review 1.  Osmosensing by bacteria: signals and membrane-based sensors.

Authors:  J M Wood
Journal:  Microbiol Mol Biol Rev       Date:  1999-03       Impact factor: 11.056

2.  Subdiffraction-limit study of Kaede diffusion and spatial distribution in live Escherichia coli.

Authors:  Somenath Bakshi; Benjamin P Bratton; James C Weisshaar
Journal:  Biophys J       Date:  2011-11-15       Impact factor: 4.033

3.  Coralline shape of the bacterial nucleoid after cryofixation.

Authors:  B Bohrmann; W Villiger; R Johansen; E Kellenberger
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

4.  Effect of cell cycle stages on the central density of Enterococcus faecium ATCC 9790.

Authors:  P Bourbeau; D Dicker; M L Higgins; L Daneo-Moore
Journal:  J Bacteriol       Date:  1989-04       Impact factor: 3.490

5.  Effect of growth rate and starvation-survival on cellular DNA, RNA, and protein of a psychrophilic marine bacterium.

Authors:  C L Moyer; R Y Morita
Journal:  Appl Environ Microbiol       Date:  1989-10       Impact factor: 4.792

6.  Study of the Deinococcus radiodurans nucleoid by cryoelectron microscopy of vitreous sections: Supplementary comments.

Authors:  Mikhail Eltsov; Jacques Dubochet
Journal:  J Bacteriol       Date:  2006-09       Impact factor: 3.490

7.  Introduction of proteins into living bacterial cells: distribution of labeled HU protein in Escherichia coli.

Authors:  V L Shellman; D E Pettijohn
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

8.  Spatial distribution and diffusive motion of RNA polymerase in live Escherichia coli.

Authors:  Benjamin P Bratton; Rachel A Mooney; James C Weisshaar
Journal:  J Bacteriol       Date:  2011-07-22       Impact factor: 3.490

9.  Axial filament formation in Bacillus subtilis: induction of nucleoids of increasing length after addition of chloramphenicol to exponential-phase cultures approaching stationary phase.

Authors:  J E Bylund; M A Haines; P J Piggot; M L Higgins
Journal:  J Bacteriol       Date:  1993-04       Impact factor: 3.490

10.  Compartmentalization of the periplasmic space at division sites in gram-negative bacteria.

Authors:  W R Cook; T J MacAlister; L I Rothfield
Journal:  J Bacteriol       Date:  1986-12       Impact factor: 3.490

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