The glucose dehydrogenase-mediated energization of Acinetobacter calcoaceticus as a tool for evaluating its susceptibility to, and defence against, hazardous chemicals

Appl Microbiol Biotechnol. 1995 Jan;42(5):738-43. doi: 10.1007/BF00171955.

Abstract

Cells of Acinetobacter calcoaceticus 69-V could be energized by glucose oxidation after the growth on acetate, ethanol, hexanol and benzoate. The velocities of glucose oxidation-driven ATP syntheses were relatively constant in the range from pH 5.4 to 7.5. With decreasing pH values (7.0, 6.0, 5.4) ATP synthesis was inhibited more strongly by the action of 2,4-dinitrophenol and at the same pH value glucose oxidation was nearly unimpaired or inhibited more weakly. This finding is expressed by a decrease of the P/O ratios, indicating the uncoupling of the electron-transport phosphorylation by 2,4-dinitrophenol. The sensitivity towards this uncoupling effect was higher in ethanol-grown cells of Acinetobacter calcoaceticus 69-V than in hexanol- or acetate-grown cells. This increase in sensitivity was accompanied by a decrease of the ratio of saturated (mainly C16:0) to unsaturated (C16:1, C18:1) fatty acids in ethanol-grown cells compared with hexanol-grown ones. The knowledge of such differences in the susceptibility and its molecular background, e.g. possible substrate-induced changes of the fatty acid composition of the cytoplasmic membranes, should help elucidate mechanisms of poisoning by membrane-active hazardous chemicals and develop defence strategies.

MeSH terms

  • 2,4-Dinitrophenol
  • Acinetobacter calcoaceticus / drug effects*
  • Acinetobacter calcoaceticus / growth & development
  • Acinetobacter calcoaceticus / metabolism*
  • Adenosine Triphosphate / biosynthesis
  • Biotechnology
  • Dinitrophenols / pharmacology
  • Electron Transport / drug effects
  • Ethanol / metabolism
  • Fatty Acids / metabolism
  • Glucose / metabolism
  • Glucose 1-Dehydrogenase
  • Glucose Dehydrogenases / metabolism*
  • Hazardous Substances / pharmacology*
  • Hexanols / metabolism
  • Hydrogen-Ion Concentration
  • Kinetics
  • Membrane Lipids / metabolism
  • Oxidation-Reduction
  • Oxygen Consumption / drug effects

Substances

  • Dinitrophenols
  • Fatty Acids
  • Hazardous Substances
  • Hexanols
  • Membrane Lipids
  • Ethanol
  • Adenosine Triphosphate
  • Glucose Dehydrogenases
  • Glucose 1-Dehydrogenase
  • Glucose
  • 2,4-Dinitrophenol