Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Aug;62(8):2687–2691. doi: 10.1128/aem.62.8.2687-2691.1996

Comamonas testosteroni colony phenotype influences exopolysaccharide production and coaggregation with yeast cells.

P Bossier 1, W Verstraete 1
PMCID: PMC168053  PMID: 8702260

Abstract

A Comamonas testosteroni strain was isolated from activated sludge on the basis of its ability to coaggregate with yeast cells. On agar plates the following two types of colonies were formed: colonies with a mucoid appearance and colonies with a nonmucoid appearance. On plates this strain alternated between the two forms, making sectored colonies. In liquid medium with constant agitation no such change was observed. In the absence of agitation and in contact with a glass surface a culture with predominantly nonmucoid-colony-forming cells very rapidly shifted to a culture dominated by mucoid-colony-forming cells. In liquid medium the reverse was observed under stress conditions imposed by hydrogen peroxide, sodium dodecyl sulfate, or starvation. Nonmucoid cells formed very rapidly settling flocs with yeast cells, while coaggregation of mucoid cells with yeast cells did not occur. These findings may be relevant to the behavior of activated sludge microbial communities.

Full Text

The Full Text of this article is available as a PDF (265.7 KB).

Selected References

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

  1. Bartlett D. H., Wright M. E., Silverman M. Variable expression of extracellular polysaccharide in the marine bacterium Pseudomonas atlantica is controlled by genome rearrangement. Proc Natl Acad Sci U S A. 1988 Jun;85(11):3923–3927. doi: 10.1073/pnas.85.11.3923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Costerton J. W., Lewandowski Z., Caldwell D. E., Korber D. R., Lappin-Scott H. M. Microbial biofilms. Annu Rev Microbiol. 1995;49:711–745. doi: 10.1146/annurev.mi.49.100195.003431. [DOI] [PubMed] [Google Scholar]
  3. Deretic V., Schurr M. J., Boucher J. C., Martin D. W. Conversion of Pseudomonas aeruginosa to mucoidy in cystic fibrosis: environmental stress and regulation of bacterial virulence by alternative sigma factors. J Bacteriol. 1994 May;176(10):2773–2780. doi: 10.1128/jb.176.10.2773-2780.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Filisetti-Cozzi T. M., Carpita N. C. Measurement of uronic acids without interference from neutral sugars. Anal Biochem. 1991 Aug 15;197(1):157–162. doi: 10.1016/0003-2697(91)90372-z. [DOI] [PubMed] [Google Scholar]
  5. Kamoun S., Kado C. I. Phenotypic Switching Affecting Chemotaxis, Xanthan Production, and Virulence in Xanthomonas campestris. Appl Environ Microbiol. 1990 Dec;56(12):3855–3860. doi: 10.1128/aem.56.12.3855-3860.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ludowieg J., Benmaman J. D. Colorimetric differentiation of hexosamines. Anal Biochem. 1967 Apr;19(1):80–88. doi: 10.1016/0003-2697(67)90136-4. [DOI] [PubMed] [Google Scholar]
  7. Martin D. W., Schurr M. J., Yu H., Deretic V. Analysis of promoters controlled by the putative sigma factor AlgU regulating conversion to mucoidy in Pseudomonas aeruginosa: relationship to sigma E and stress response. J Bacteriol. 1994 Nov;176(21):6688–6696. doi: 10.1128/jb.176.21.6688-6696.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Masy C. L., Henquinet A., Mestdagh M. M. Flocculation of Saccharomyces cerevisiae: inhibition by sugars. Can J Microbiol. 1992 Dec;38(12):1298–1306. doi: 10.1139/m92-214. [DOI] [PubMed] [Google Scholar]
  9. Moxon E. R., Rainey P. B., Nowak M. A., Lenski R. E. Adaptive evolution of highly mutable loci in pathogenic bacteria. Curr Biol. 1994 Jan 1;4(1):24–33. doi: 10.1016/s0960-9822(00)00005-1. [DOI] [PubMed] [Google Scholar]
  10. SCHATZ A., BOVELL C., Jr Growth and hydrogenase activity of a new bacterium, Hydrogenomonas facilis. J Bacteriol. 1952 Jan;63(1):87–98. doi: 10.1128/jb.63.1.87-98.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Spalding A., Tuite M. F. Host-plasmid interactions in Saccharomyces cerevisiae: effect of host ploidy on plasmid stability and copy number. J Gen Microbiol. 1989 Apr;135(4):1037–1045. doi: 10.1099/00221287-135-4-1037. [DOI] [PubMed] [Google Scholar]
  12. Sullam P. M., Costerton J. W., Yamasaki R., Dazin P. F., Mills J. Inhibition of platelet binding and aggregation by streptococcal exopolysaccharide. J Infect Dis. 1993 May;167(5):1123–1130. doi: 10.1093/infdis/167.5.1123. [DOI] [PubMed] [Google Scholar]
  13. Top E., Mergeay M., Springael D., Verstraete W. Gene escape model: transfer of heavy metal resistance genes from Escherichia coli to Alcaligenes eutrophus on agar plates and in soil samples. Appl Environ Microbiol. 1990 Aug;56(8):2471–2479. doi: 10.1128/aem.56.8.2471-2479.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Zita A., Hermansson M. Effects of ionic strength on bacterial adhesion and stability of flocs in a wastewater activated sludge system. Appl Environ Microbiol. 1994 Sep;60(9):3041–3048. doi: 10.1128/aem.60.9.3041-3048.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES