Larger increases in sensitivity to paracatalytic inactivation than in catalytic competence during experimental evolution of the second beta-galactosidase of Escherichia coli

Biochem J. 1997 Jul 1;325 ( Pt 1)(Pt 1):117-21. doi: 10.1042/bj3250117.

Abstract

Second-order rate constants (M-1.s-1) at 25 degrees C and pH 7.5 for inactivation of first-generation (ebga and ebgb), second-generation (ebgab and ebgabcd) and third-generation (ebgabcde) experimental evolvants of the title enzyme by 2',4'-dinitrophenyl 2-deoxy-2-fluoro-beta-D-galactopyranoside are 0.042, 0.30, 10, 24 and 57 respectively. Only partial inactivation is observed, except for ebgabcde. At a single high inactivator concentration, inactivation of the wild-type ebgo is also seen. The changes in sensitivity to the paracatalytic inactivator (over a range of 10(3.3)) are larger than changes in kcat/Km for lactose (over a range of 10(2.7)) or nitrophenyl galactosides (over a range of only 10(1.3)), or changes in degalactosylation rate (over a range of 10(1.7)). These data raise the possibility that evolution in the reverse sense, towards insensitivity to a paracatalytic inactivator with a proportionally lower effect on transformation of substrate, may become a mechanism for the development of bacterial resistance to antibiotics that act by paracatalytic enzyme inactivation.

Publication types

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

MeSH terms

  • Binding Sites
  • Escherichia coli / enzymology*
  • Hydrogen-Ion Concentration
  • Isoenzymes / antagonists & inhibitors*
  • Kinetics
  • Molecular Structure
  • Nitrophenylgalactosides / pharmacology*
  • beta-Galactosidase / antagonists & inhibitors*

Substances

  • Isoenzymes
  • 2',4'-dinitrophenyl 2-deoxy-2-fluorogalactopyranoside
  • Nitrophenylgalactosides
  • beta-Galactosidase