Literature DB >> 3539913

Organization of developing Escherichia coli colonies viewed by scanning electron microscopy.

J A Shapiro.   

Abstract

Colony growth was initiated by inoculating minimal glucose agar with 1-microliter. spots of a plasmid-free Escherichia coli culture and incubating at 32 degrees C. Inoculations took place over a 3-day period, at the end of which the plates were fixed and dried for scanning electron microscopy. In this way, it was possible to examine the surfaces of colonies ranging in age from 0 to 68 h. Macroscopically, the colonies were organized into different concentric zones, and several morphological features could be seen to develop over this period. These included a shallow depression ring marking the site of inoculation, a deeper indentation ring whose position moved outward as the colony grew, an expanding plateau region between the two rings, a mound outside the indentation ring, and a flat brim extending onto the substrate which was either present or absent at different times. Microscopically, a variety of cell morphologies and cell arrangements were detected. Upon inoculation, the bacteria accumulated at the periphery of the inoculation spot but showed no other kind of order. For the first 7.5 h, all bacteria were rod shaped; at the end of this initial phase, a high degree of alignment was seen in the cells at the colony edge. By 24.5 h, both shorter more ovoid cells and longer filaments had begun to appear, and large multicellular arrays had formed. At later stages of colony development, morphologically distinguishable zones involving cells of different shapes and sizes had formed, and these zones often marked the boundaries of macroscopic features. The edges were particularly interesting and at 68 h displayed very sharp saw-toothed boundaries between concentrically organized groups of bacteria. There were some transient irregularities in the concentric organizations of growing colonies, and one colony had entered upon a distinct developmental pathway.

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Year:  1987        PMID: 3539913      PMCID: PMC211746          DOI: 10.1128/jb.169.1.142-156.1987

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


  10 in total

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Authors:  J F HOENIGER
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Authors:  H HOFFMAN; M E FRANK
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Review 4.  Nature of the swarming phenomenon in Proteus.

Authors:  F D Williams; R H Schwarzhoff
Journal:  Annu Rev Microbiol       Date:  1978       Impact factor: 15.500

5.  [Expansion phenomena of proteus cultures. II. The pushing expansion (author's transl)].

Authors:  S Sturdza
Journal:  Zentralbl Bakteriol Orig A       Date:  1977-08

6.  Development of concentric zones in the Proteus swarm colony.

Authors:  C W Douglas; K A Bisset
Journal:  J Med Microbiol       Date:  1976-11       Impact factor: 2.472

7.  Scanning electron microscope study of Pseudomonas putida colonies.

Authors:  J A Shapiro
Journal:  J Bacteriol       Date:  1985-12       Impact factor: 3.490

8.  A continuous study of morphological phase in the swarm of Proteus.

Authors:  K A Bisset; C W Douglas
Journal:  J Med Microbiol       Date:  1976-05       Impact factor: 2.472

9.  High-frequency switching of colony morphology in Candida albicans.

Authors:  B Slutsky; J Buffo; D R Soll
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10.  The use of Mudlac transposons as tools for vital staining to visualize clonal and non-clonal patterns of organization in bacterial growth on agar surfaces.

Authors:  J A Shapiro
Journal:  J Gen Microbiol       Date:  1984-05
  10 in total
  19 in total

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Authors:  J A Shapiro
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8.  Differential activity of a transposable element in Escherichia coli colonies.

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