Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1997 Jun;63(6):2347–2354. doi: 10.1128/aem.63.6.2347-2354.1997

Light-induced motility of thermophilic Synechococcus isolates from Octopus Spring, Yellowstone National Park.

N B Ramsing 1, M J Ferris 1, D M Ward 1
PMCID: PMC168527  PMID: 11536814

Abstract

This study demonstrates light-induced motility of two thermophilic Synechococcus isolates that are morphologically similar but that belong to different cyanobacterial lineages. Both isolates migrated away from densely inoculated streaks to form fingerlike projections extending toward or away from the light source, depending on the light intensity. However, the two isolates seemed to prefer widely different light conditions. The behavior of each isolate was controlled by several factors, including temperature, preacclimation of inocula, acclimation during the experiment, and strain-specific genetic preferences for different light conditions (adaptation). Time-lapse microscopy confirmed that these projections were formed by actively gliding cells and were not simply the outcome of directional cell division. The observed motility rates of individual cells of 0.1 to 0.3 micrometers s-1 agreed well with the distance traversed by the projections, 0.3 to 0.5 mm h-1, suggesting that most cells in each projection are travelling in the same direction. The finding of motility among two phylogenetically unaffiliated unicellular cyanobacteria suggests that this trait may be widespread among this group. If so, this would have important implications for experiments on colonization, succession, diel positioning, and photosynthetic activity in hot spring mats dominated by Synechococcus-like cyanobacteria.

Full Text

The Full Text of this article is available as a PDF (868.4 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bebout B. M., Garcia-Pichel F. UV B-Induced Vertical Migrations of Cyanobacteria in a Microbial Mat. Appl Environ Microbiol. 1995 Dec;61(12):4215–4222. doi: 10.1128/aem.61.12.4215-4222.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ferris M. J., Muyzer G., Ward D. M. Denaturing gradient gel electrophoresis profiles of 16S rRNA-defined populations inhabiting a hot spring microbial mat community. Appl Environ Microbiol. 1996 Feb;62(2):340–346. doi: 10.1128/aem.62.2.340-346.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ferris M. J., Nold S. C., Revsbech N. P., Ward D. M. Population structure and physiological changes within a hot spring microbial mat community following disturbance. Appl Environ Microbiol. 1997 Apr;63(4):1367–1374. doi: 10.1128/aem.63.4.1367-1374.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ferris M. J., Ruff-Roberts A. L., Kopczynski E. D., Bateson M. M., Ward D. M. Enrichment culture and microscopy conceal diverse thermophilic Synechococcus populations in a single hot spring microbial mat habitat. Appl Environ Microbiol. 1996 Mar;62(3):1045–1050. doi: 10.1128/aem.62.3.1045-1050.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Häder D. P. Photosensory behavior in procaryotes. Microbiol Rev. 1987 Mar;51(1):1–21. doi: 10.1128/mr.51.1.1-21.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Nold S. C., Ward D. M. Photosynthate partitioning and fermentation in hot spring microbial mat communities. Appl Environ Microbiol. 1996 Dec;62(12):4598–4607. doi: 10.1128/aem.62.12.4598-4607.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ruff-Roberts A. L., Kuenen J. G., Ward D. M. Distribution of cultivated and uncultivated cyanobacteria and Chloroflexus-like bacteria in hot spring microbial mats. Appl Environ Microbiol. 1994 Feb;60(2):697–704. doi: 10.1128/aem.60.2.697-704.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Stanier R. Y., Kunisawa R., Mandel M., Cohen-Bazire G. Purification and properties of unicellular blue-green algae (order Chroococcales). Bacteriol Rev. 1971 Jun;35(2):171–205. doi: 10.1128/br.35.2.171-205.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ward D. M., Santegoeds C. M., Nold S. C., Ramsing N. B., Ferris M. J., Bateson M. M. Biodiversity within hot spring microbial mat communities: molecular monitoring of enrichment cultures. Antonie Van Leeuwenhoek. 1997 Feb;71(1-2):143–150. doi: 10.1023/a:1000131426164. [DOI] [PubMed] [Google Scholar]
  10. Ward D. M., Weller R., Bateson M. M. 16S rRNA sequences reveal numerous uncultured microorganisms in a natural community. Nature. 1990 May 3;345(6270):63–65. doi: 10.1038/345063a0. [DOI] [PubMed] [Google Scholar]
  11. Waterbury J. B., Stanier R. Y. Patterns of growth and development in pleurocapsalean cyanobacteria. Microbiol Rev. 1978 Mar;42(1):2–44. doi: 10.1128/mr.42.1.2-44.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES