Interactions between the soluble domain I of nicotinamide nucleotide transhydrogenase from Rhodospirillum rubrum and transhydrogenase from Escherichia coli. Effects on catalytic and H+-pumping activities

Eur J Biochem. 2000 Jun;267(11):3281-8. doi: 10.1046/j.1432-1327.2000.01358.x.

Abstract

Nicotinamide nucleotide transhydrogenase from Escherichia coli is composed of two subunits, the alpha and the beta subunits, each of which contains a hydrophilic domain, domain I and III, respectively, as well as several transmembrane helices, collectively denoted domain II. The interactions between domain I from Rhodospirillum rubrum (rrI) and the intact or the protease-treated enzyme from E. coli was investigated using the separately expressed and purified domain I from R. rubrum, and His-tagged intact and trypsin-treated E. coli transhydrogenase. Despite harsh treatments with, e.g. detergents and denaturing agents, the alpha and beta subunits remained tightly associated. A monoclonal antibody directed towards the alpha subunit was strongly inhibitory, an effect that was relieved by added rrI. In addition, rrI also reactivated the trypsin-digested E. coli enzyme in which domain I had been partly removed. This suggests that the hydrophilic domains I and III are not in permanent contact but are mobile during catalysis while being anchored to domain II. Replacement of domain I of intact, as well as trypsin-digested, E. coli transhydrogenase with rrI resulted in a markedly different pH dependence of the cyclic reduction of 3-acetyl-pyridine-NAD+ by NADH in the presence of NADP(H), suggesting that the protonation of one or more protonable groups in domain I is controlling this reaction. The reverse reaction and proton pumping showed a less pronounced change in pH dependence, demonstrating the regulatory role of domain II in these reactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Bacterial / pharmacology
  • Antibodies, Monoclonal / pharmacology
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / immunology
  • Bacterial Proteins / metabolism*
  • Catalysis
  • Detergents / pharmacology
  • Escherichia coli / enzymology*
  • Hydrogen-Ion Concentration
  • Liposomes
  • Mice
  • Mice, Inbred BALB C
  • Models, Molecular
  • Molecular Sequence Data
  • NAD / analogs & derivatives
  • NAD / metabolism
  • NADP / metabolism
  • NADP Transhydrogenases / chemistry
  • NADP Transhydrogenases / immunology
  • NADP Transhydrogenases / metabolism*
  • Protein Binding
  • Protein Conformation
  • Protein Denaturation
  • Protein Multimerization
  • Protein Structure, Tertiary
  • Protons
  • Recombinant Fusion Proteins / metabolism
  • Rhodospirillum rubrum / enzymology*
  • Trypsin / pharmacology

Substances

  • Antibodies, Bacterial
  • Antibodies, Monoclonal
  • Bacterial Proteins
  • Detergents
  • Liposomes
  • Protons
  • Recombinant Fusion Proteins
  • NAD
  • NADP
  • 3-acetylpyridine adenine dinucleotide
  • NADP Transhydrogenases
  • Trypsin