Nickel and cobalt resistance engineered in Escherichia coli by overexpression of serine acetyltransferase from the nickel hyperaccumulator plant Thlaspi goesingense

Appl Environ Microbiol. 2005 Dec;71(12):8627-33. doi: 10.1128/AEM.71.12.8627-8633.2005.

Abstract

The overexpression of serine acetyltransferase from the Ni-hyperaccumulating plant Thlaspi goesingense causes enhanced nickel and cobalt resistance in Escherichia coli. Furthermore, overexpression of T. goesingense serine acetyltransferase results in enhanced sensitivity to cadmium and has no significant effect on resistance to zinc. Enhanced nickel resistance is directly related to the constitutive overactivation of sulfur assimilation and glutathione biosynthesis, driven by the overproduction of O-acetyl-L-serine, the product of serine acetyltransferase and a positive regulator of the cysteine regulon. Nickel in the serine acetyltransferase-overexpressing strains is not detoxified by coordination or precipitation with sulfur, suggesting that glutathione is involved in reducing the oxidative damage imposed by nickel.

Publication types

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

MeSH terms

  • Cobalt / pharmacology*
  • DNA, Complementary / genetics
  • DNA, Plant / genetics
  • Drug Resistance, Bacterial
  • Escherichia coli / drug effects*
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Escherichia coli / metabolism
  • Gene Expression Regulation, Bacterial*
  • Gene Expression Regulation, Enzymologic
  • Genetic Engineering
  • Glutathione / metabolism
  • Kinetics
  • Nickel / metabolism
  • Nickel / pharmacology*
  • Serine O-Acetyltransferase / genetics*
  • Sulfur / metabolism
  • Thlaspi / drug effects
  • Thlaspi / enzymology
  • Thlaspi / genetics*
  • Thlaspi / microbiology

Substances

  • DNA, Complementary
  • DNA, Plant
  • Cobalt
  • Sulfur
  • Nickel
  • Serine O-Acetyltransferase
  • Glutathione