Relation of chemotactic response to the amount of receptor: evidence for different efficiencies of signal transduction

J Bacteriol. 1979 Jun;138(3):739-47. doi: 10.1128/jb.138.3.739-747.1979.

Abstract

We determined the content of galactose-glucose-, maltose-, and ribose-binding proteins in cells of Escherichia coli K-12 grown in a variety of media and also measured the respective transport and chemotactic activities that depend on those binding proteins. Correlation of the level of induction of a particular binding protein with the extent of tactic activity mediated by that protein indicates that the magnitude of the tactic response to a particular stimulating compound is a direct function of the number of receptors per cell. In contrast, comparison of the magnitudes of response to substances recognized by independent receptors indicates that some stimulus-receptor complexes are more effective in eliciting tactic responses than are others. Thus, the magnitude of response to any particular stimulating compound is a function both of the number of receptors per cell and of the effectiveness of the stimulus-receptor complex. Considerations of available information about the tactic response to maltose suggest that the effectiveness of a stimulus-receptor complex is related to the transducer with which the receptor interacts. The tar product appears to be a relatively effective transducer of the signals it accepts from receptors for aspartate, alpha-methylaspartate, and maltose, whereas the trg product appears to be a relatively ineffective transducer of signals it accepts from receptors for galactose and ribose.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bacterial Proteins / analysis*
  • Bacterial Proteins / metabolism
  • Chemotaxis*
  • Escherichia coli / analysis
  • Escherichia coli / physiology*
  • Galactose / metabolism
  • Glucose / metabolism
  • Maltose / metabolism
  • Osmotic Pressure
  • Receptors, Drug / analysis*
  • Receptors, Drug / metabolism
  • Ribose / metabolism

Substances

  • Bacterial Proteins
  • Receptors, Drug
  • Ribose
  • Maltose
  • Glucose
  • Galactose