Literature DB >> 2427501

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

M L Higgins, A L Koch, D T Dicker, L Daneo-Moore.   

Abstract

Mid-exponential-phase cultures were either labeled continuously with tritiated leucine and uracil or pulse-labeled with tritiated leucine. The amount of leucine and uracil incorporated into protein or RNA per cell was determined by grain counts of autoradiographs of cells seen in electron micrographs; the volume of each cell was determined by three-dimensional reconstruction. The average number of autoradiographic grains around cells continuously labeled with uracil and leucine increased linearly with cell volume. In contrast, while the average grain count around cells pulse-labeled with leucine increased in a near-linear fashion over most of the volume classes, less than the expected number of grains were seen around cells in large- and small-size classes. The distribution of grains around cells from both the continuously and pulse-labeled populations could be fit at the 5% confidence level with a Poisson distribution modified to take into consideration the volume distribution of each population of cells analyzed. These findings suggested that large changes in the density of RNA and protein do not occur in most cells as they increase in size; however, there may be decreases in the rate of protein synthesis in some large and small cells. The decrease in the rate of protein synthesis appears consistent with the hypothesis that new sites of envelope growth must be introduced into cells that are close to the division event to restore rapid growth.

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Year:  1986        PMID: 2427501      PMCID: PMC215965          DOI: 10.1128/jb.167.3.960-967.1986

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


  22 in total

Review 1.  Does the initiation of chromosome replication regulate cell division?

Authors:  A L Koch
Journal:  Adv Microb Physiol       Date:  1977       Impact factor: 3.517

2.  A reliable, standardized method for ultrastructural electron microscopic radioautography.

Authors:  B M Kopriwa
Journal:  Histochemie       Date:  1973-10-03

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

Authors:  R P Hinks; L Daneo-Moore; G D Shockman
Journal:  J Bacteriol       Date:  1978-02       Impact factor: 3.490

4.  Biochemical determination of bacterial morphology and the geometry of cell division.

Authors:  E P Previc
Journal:  J Theor Biol       Date:  1970-06       Impact factor: 2.691

5.  Three-dimensional reconstruction of whole cells of Streptococcus faecalis from thin sections of cells.

Authors:  M L Higgins
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

6.  Study of cycle of cell wall assembly in Streptococcus faecalis by three-dimensional reconstructions of thin sections of cells.

Authors:  M L Higgins; G D Shockman
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

7.  DNA replication pattern and cell wall growth in Escherichia coli PAT 84.

Authors:  L J Koppes; N Overbeeke; N Nanninga
Journal:  J Bacteriol       Date:  1978-03       Impact factor: 3.490

8.  Model for cell wall growth of Streptococcus faecalis.

Authors:  M L Higgins; G D Shockman
Journal:  J Bacteriol       Date:  1970-02       Impact factor: 3.490

9.  Quantitative radioautographic studies on exponentially growing cultures of Escherichia coli. The distribution of parental DNA, RNA, protein, and cell wall among progeny cells.

Authors:  R P VAN TUBERGEN; R B SETLOW
Journal:  Biophys J       Date:  1961-09       Impact factor: 4.033

10.  Kinetics of growth of individual cells of Escherichia coli and Azotobacter agilis.

Authors:  R J Harvey; A G Marr; P R Painter
Journal:  J Bacteriol       Date:  1967-02       Impact factor: 3.490

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  4 in total

1.  Relationship between changes in buoyant density and formation of new sites of cell wall growth in cultures of streptococci (Enterococcus hirae ATCC 9790) undergoing a nutritional shift-up.

Authors:  M L Higgins; M Haines; M Whalen; D Glaser; J Bylund
Journal:  J Bacteriol       Date:  1990-08       Impact factor: 3.490

2.  Measurement of live bacteria by Nomarski interference microscopy and stereologic methods as tested with macroscopic rod-shaped models.

Authors:  W W Baldwin; P W Bankston
Journal:  Appl Environ Microbiol       Date:  1988-01       Impact factor: 4.792

3.  Autoradiographic studies of chromosome replication during the cell cycle of Streptococcus faecium.

Authors:  M L Higgins; A L Koch; D T Dicker; L Daneo-Moore
Journal:  J Bacteriol       Date:  1986-11       Impact factor: 3.490

4.  Cell cycle changes in the buoyant density of exponential-phase cells of Streptococcus faecium.

Authors:  D T Dicker; M L Higgins
Journal:  J Bacteriol       Date:  1987-03       Impact factor: 3.490

  4 in total

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