Literature DB >> 332295

Flow-microfluorometric analysis of Escherichia coli, Rhizobium meliloti, and Rhizobium japonicum at different stages of the growth cycle.

A S Paau, J R Cowles, J Oro.   

Abstract

The applicability of flow-microfluorometry (FMF) to the study of bacterial samples was investigated on cultures of Rhizobium meliloti, Rhizobium japonicum, and Escherichia coli using fluorescent and light-scattering signals. This technique which analyzes individual bacterial cells in a population was used to monitor the relative change in nucleic acid content and cell size during the growth cycle of the three microorganisms which were known to have different growth rates. Early log-phase E. coli cells contained at least eightfold more nucleic acid and were significantly larger than the stationary-phase cells. Cultures of early log-phase R. meliloti cells contained three to four-fold more nucleic acid and were slightly larger than cells in the stationary phase. Rhizobium japonicum had very little change in either parameter. In general, the amount of change in both cell size and nucleic acid content upon initiation of log-phase growth was related to the overall growt rate of the organisms, with E. coli experiencing the greatest change and R. japonicum the least. Results obtained by FMF analysis, therefore, were consistent with observations reported by earlier workers. Cultures of R. meliloti also were used to demonstrate that the intensity of the fluorescent signals was sensitive to digestion by DNase and RNase and to prolonged storage and fixation. The potential use of FMF in the study of microorganisms is discussed.

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Year:  1977        PMID: 332295     DOI: 10.1139/m77-175

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  11 in total

1.  Separation of algal mixtures and bacterial mixtures with flow-microfluorometer using chlorophyll and ethidium bromide fluorescence.

Authors:  A S Paau; J R Cowles; J Oro; A Bartel; E Hungerford
Journal:  Arch Microbiol       Date:  1979-03-12       Impact factor: 2.552

2.  Microcultural study of bacterial size changes and microcolony and ultramicrocolony formation by heterotrophic bacteria in seawater.

Authors:  F Torrella; R Y Morita
Journal:  Appl Environ Microbiol       Date:  1981-02       Impact factor: 4.792

Review 3.  Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses.

Authors:  H M Davey; D B Kell
Journal:  Microbiol Rev       Date:  1996-12

4.  Flow microfluorometry study of diauxic batch growth of Saccharomyces cerevisiae.

Authors:  M F Gilbert; D N McQuitty; J E Bailey
Journal:  Appl Environ Microbiol       Date:  1978-10       Impact factor: 4.792

Review 5.  Fundamental principles in bacterial physiology-history, recent progress, and the future with focus on cell size control: a review.

Authors:  Suckjoon Jun; Fangwei Si; Rami Pugatch; Matthew Scott
Journal:  Rep Prog Phys       Date:  2018-01-09

6.  Development of Bacteroids in Alfalfa (Medicago sativa) Nodules.

Authors:  A S Paau; J R Cowles
Journal:  Plant Physiol       Date:  1978-10       Impact factor: 8.340

7.  Escherichia coli growth studied by dual-parameter flow cytophotometry.

Authors:  H B Steen; E Boye
Journal:  J Bacteriol       Date:  1981-02       Impact factor: 3.490

8.  DNA content of free living rhizobia and bacteroids of various Rhizobium-legume associations.

Authors:  A S Paau; J Oro; J R Cowles
Journal:  Plant Physiol       Date:  1979-02       Impact factor: 8.340

9.  Flow cytometric determinations of cellular substances in algae, bacteria, moulds and yeasts.

Authors:  K J Hutter; H E Eipel
Journal:  Antonie Van Leeuwenhoek       Date:  1978       Impact factor: 2.271

10.  Changes of ploidy during the Azotobacter vinelandii growth cycle.

Authors:  R Maldonado; J Jiménez; J Casadesús
Journal:  J Bacteriol       Date:  1994-07       Impact factor: 3.490

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