Amino acid-dependent transport of sugars by Fusobacterium nucleatum ATCC 10953

J Bacteriol. 1987 Sep;169(9):3891-7. doi: 10.1128/jb.169.9.3891-3897.1987.

Abstract

Resting cells of Fusobacterium nucleatum 10953 (grown previously in a medium containing glucose) failed to accumulate glucose under aerobic or anaerobic conditions. However, the addition of glutamic acid, lysine, or histidine to anaerobic suspensions of cells caused the immediate and rapid accumulation of glucose. Except for the amino acid-dependent transport of galactose and fructose (the latter being transported at approximately one-third the rate of glucose), no other sugars tested were accumulated by the resting cells. Amino acid-dependent uptake of sugar(s) by F. nucleatum was abolished by exposure of cells to air, and under aerobic conditions the rates of fermentation of glutamic acid and lysine were less than 15% of the rates determined anaerobically. The energy necessary for active transport of the sugars (acetyl phosphate and ATP) is derived from the anaerobic fermentation of glutamic acid, lysine, or histidine. Competition studies revealed that glucose and galactose were mutual and exclusive inhibitors of transport, and it is suggested that the two sugars (Km = 14 microM) are translocated via a common carrier. The products of amino acid-dependent sugar transport were recovered from resting cells as ethanol-precipitable, high-molecular-weight polymers. Polymer formation by F. nucleatum, during growth in medium containing glucose or galactose, was confirmed by electron microscopy.

MeSH terms

  • Aerobiosis
  • Amino Acids / metabolism*
  • Anaerobiosis
  • Biological Transport, Active
  • Fermentation
  • Fructose / metabolism
  • Fusobacterium / metabolism*
  • Fusobacterium / ultrastructure
  • Galactose / metabolism*
  • Glucose / metabolism*
  • Glutamates / metabolism
  • Histidine / metabolism
  • Kinetics
  • Lysine / metabolism
  • Microscopy, Electron

Substances

  • Amino Acids
  • Glutamates
  • Fructose
  • Histidine
  • Glucose
  • Lysine
  • Galactose