Isolation and characterization of temperature-sensitive pantothenate kinase (coaA) mutants of Escherichia coli

J Bacteriol. 1987 Dec;169(12):5795-800. doi: 10.1128/jb.169.12.5795-5800.1987.

Abstract

Escherichia coli mutants conditionally defective in the conversion of pantothenate to coenzyme A were isolated and characterized. The gene was designated coaA and localized between argEH and rpoB near min 90 of the chromosome. The coaA15(Ts) mutation caused a temperature-sensitive growth phenotype and temperature-dependent inactivation of pantothenate kinase activity assayed both in vivo and in vitro. At 30 degrees C, coaA15(Ts) extracts contained less than 20% of the wild-type pantothenate kinase activity; the kinase had near normal kinetic constants for the substrates ATP and pantothenate and was inhibited by coenzyme A to the same degree as the wild-type enzyme. These data define the coaA gene as the structural gene for pantothenate kinase.

Publication types

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

MeSH terms

  • Coenzyme A / metabolism
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Genes*
  • Genes, Bacterial
  • Mutation
  • Pantothenic Acid / metabolism
  • Phenotype
  • Phosphorylation
  • Phosphotransferases (Alcohol Group Acceptor)*
  • Phosphotransferases / genetics*
  • Temperature
  • Transduction, Genetic
  • beta-Alanine / metabolism

Substances

  • beta-Alanine
  • Pantothenic Acid
  • Phosphotransferases
  • Phosphotransferases (Alcohol Group Acceptor)
  • pantothenate kinase
  • Coenzyme A