Literature DB >> 13921527

Cell multiplication studied with an electronic particle counter.

G TOENNIES, L ISZARD, N B ROGERS, G D SHOCKMAN.   

Abstract

Toennies, G. (Institute for Cancer Research, Philadelphia, Pa.), L. Iszard, N. B. Rogers, and G. D. Shockman. Cell multiplication studied with an electronic particle counter. J. Bacteriol. 82:857-866. 1961.-Suitable conditions are described for the application of the Counter electronic particle counter to the study of bacterial number and particle size distribution in growing cultures. When Streptococcus faecalis and Escherichia coli were each grown in a different medium, exponential growth was accompanied by a continuous decrease in average particle size. The average apparent particle volume of S. faecalis decreased by about 50% in five generations. Microscopic studies of S. faecalis indicated that this was due to a decrease in the average chain length of the cultures. The following observations concerning average particle size during exponential growth of S. faecalis in a synthetic medium were made: (i) A decreased concentration of tryptophan, serine, or proline resulted in a significant decrease in average particle size. Similar changes in numerous other nutrients produced no or only minor changes. (ii) The addition of a cytoplasmic extract prepared from exponentially growing cells resulted in changes similar to those resulting from the partial withdrawal from the medium of certain nutrients. (iii) The effect of the cytoplasmic extract could be counteracted by the addition of tryptophan. (iv) A limited survey, including the effects of the rate of exponential growth, mechanical agitation, the presence of indoleacetic acid, indole, kinetin, lysozyme, or ascorbate, disclosed no additional factor which significantly influenced the particle size distribution.

Entities:  

Keywords:  BACTERIOLOGICAL TECHNIQUES; ESCHERICHIA COLI/culture; STREPTOCOCCUS FAECALIS/culture

Mesh:

Year:  1961        PMID: 13921527      PMCID: PMC279268          DOI: 10.1128/jb.82.6.857-866.1961

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


  14 in total

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3.  Bacterial cell wall synthesis: the effect of threonine depletion.

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Journal:  J Biol Chem       Date:  1959-09       Impact factor: 5.157

4.  Avoidance of alkaline effects in cell disruption by glass beads.

Authors:  J J KOLB
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5.  A high speed shaker for the disruption of cells at low temperatures.

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7.  Quantitative amino acid assimilation in homofermentative metabolism.

Authors:  G TOENNIES; G D SHOCKMAN
Journal:  Arch Biochem Biophys       Date:  1953-08       Impact factor: 4.013

8.  The influence of magnesium on cell division. VI. The action of certain hydrolytic enzymes on the filamentous and chain forms of gram-positive rod-shaped organisms.

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9.  The Estimation of Bacterial Populations with the Aid of a Photoelectric Densitometer.

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Journal:  J Bacteriol       Date:  1936-09       Impact factor: 3.490

10.  Chemical studies in host-virus interactions; a comparison of some properties of three mutant pairs of bacterial viruses, T2r and T2r, T4r and T4r, T6r and T6r.

Authors:  S S COHEN; R ARBOGAST
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  20 in total

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Authors:  G J Mountney; J O'malley
Journal:  Appl Microbiol       Date:  1966-11

2.  Autoradiographic studies of the synthesis of RNA and protein as a function of cell volume in Streptococcus faecium.

Authors:  M L Higgins; A L Koch; D T Dicker; L Daneo-Moore
Journal:  J Bacteriol       Date:  1986-09       Impact factor: 3.490

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4.  Morphokinetic reaction of cells of Streptococcus faecalis (ATCC 9790) to specific inhibition of macromolecular synthesis: dependence of mesosome growth on deoxyribonucleic acid synthesis.

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Journal:  J Bacteriol       Date:  1972-03       Impact factor: 3.490

5.  Cellular autolytic activity in synchronized populations of Streptococcus faecium.

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Review 6.  Symposium on the fine structure and replication of bacteria and their parts. IV. Unbalanced cell-wall synthesis: autolysis and cell-wall thickening.

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7.  [A method for counting thrombocytes in the blood by means of an automatic particle counter].

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8.  Analysis of initiation of sites of cell wall growth in Streptococcus faecium during a nutritional shift.

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Journal:  J Bacteriol       Date:  1984-12       Impact factor: 3.490

9.  Characterization of structural variations in the peptidoglycan of vancomycin-susceptible Enterococcus faecium: understanding glycopeptide-antibiotic binding sites using mass spectrometry.

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10.  Relationship of shape to initiation of new sites of envelope growth in Streptococcus faecium cells treated with beta-lactam antibiotics.

Authors:  M L Higgins; M Ferrero; L Daneo-Moore
Journal:  J Bacteriol       Date:  1986-08       Impact factor: 3.490

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