Regulation of hexitol catabolism in Streptococcus mutans

J Bacteriol. 1983 Feb;153(2):861-6. doi: 10.1128/jb.153.2.861-866.1983.

Abstract

Regulation of hexitol catabolism was investigated in Streptococcus mutans, a cariogenic human dental plaque bacterium. Induction of hexitol catabolic enzymes and phosphoenolpyruvate:hexitol phosphotransferase and hexitol phosphate dehydrogenase activities was regulated by an inducer exclusion mechanism initiated by D-glucose and 2-deoxy-D-glucose. Kinetic analysis of the inhibitory effect of 2-deoxy-D-glucose on initial hexitol uptake illustrated that this was a noncompetitive type of inhibition. In mutant strains of S. mutans lacking phosphoenolpyruvate:glucose phosphotransferase activity, 2-deoxy-D-glucose was unable to inhibit hexitol uptake. These observations provide evidence for possible molecular mechanisms for the exclusion process.

MeSH terms

  • Biological Transport / drug effects
  • Deoxy Sugars / pharmacology*
  • Deoxyglucose / pharmacology*
  • Enzyme Induction
  • Escherichia coli Proteins
  • Glucose / metabolism
  • Glucose / pharmacology*
  • Lactates / metabolism
  • Lactic Acid
  • Mannitol / metabolism*
  • Monosaccharide Transport Proteins
  • Phosphoenolpyruvate Sugar Phosphotransferase System / biosynthesis
  • Sorbitol / metabolism*
  • Streptococcus mutans / metabolism*
  • Sugar Alcohol Dehydrogenases / biosynthesis

Substances

  • Deoxy Sugars
  • Escherichia coli Proteins
  • Lactates
  • Monosaccharide Transport Proteins
  • Lactic Acid
  • Mannitol
  • Sorbitol
  • Deoxyglucose
  • Sugar Alcohol Dehydrogenases
  • sorbitol-6-phosphate dehydrogenase
  • mannitol-1-phosphate dehydrogenase
  • Phosphoenolpyruvate Sugar Phosphotransferase System
  • mannitol PTS permease, E coli
  • phosphoenolpyruvate-sorbitol phosphotransferase
  • Glucose