Starvation-specific formation of a peripheral exopolysaccharide by a marine Pseudomonas sp., strain S9

Appl Environ Microbiol. 1990 Jul;56(7):2065-72. doi: 10.1128/aem.56.7.2065-2072.1990.

Abstract

The marine bacterium Pseudomonas sp. strain S9 produces exopolysaccharides (EPS) during both growth and total energy source and nutrient starvation. Transmission electron microscopy of immunogold-labeled cells demonstrated that the EPS is closely associated with the cell surface during growth (integral EPS), while both the integral form and a loosely associated extracellular (peripheral) form were observed during starvation. Formation and release of the latter rendered the starvation medium viscous. In addition, after 3 h of starvation in static conditions, less than 5% of the cells were motile, compared with 100% at the onset of starvation and approximately 80% subsequent to release of the peripheral EPS at 27 h of starvation. Inhibition of protein synthesis with chloramphenicol added before 3 h of starvation caused no increase in viscosity. However, addition of chloramphenicol at 3 h did not prevent the subsequent increase in viscosity displayed by S9 cells. The amount of integral EPS increased for both nontreated and chloramphenicol-treated S9 cells during the first hour of starvation, with a subsequent equal decrease. The chloramphenicol-treated cells, as well as cells of a transposon-generated mutant strain deficient in peripheral EPS formation, remained adhesive to a hydrophobic inanimate surface during the initial 5 h of starvation, whereas nontreated wild-type cells had progressively decreased adhesion capacity. During the initial 5 h of starvation, most of the nontreated cells but only a small fraction of the chloramphenicol-treated and mutant cells detached from the hydrophobic substratum.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / biosynthesis
  • Cell Adhesion / physiology
  • Cell Movement / physiology
  • Chloramphenicol / pharmacology
  • Immunoenzyme Techniques
  • Polysaccharides, Bacterial / biosynthesis*
  • Pseudomonas / drug effects
  • Pseudomonas / growth & development
  • Pseudomonas / metabolism*

Substances

  • Bacterial Proteins
  • Polysaccharides, Bacterial
  • Chloramphenicol