Electrostatic interactions across the dimer-dimer interface contribute to the pH-dependent stability of a tetrameric malate dehydrogenase

FEBS Lett. 2003 Oct 23;553(3):423-6. doi: 10.1016/s0014-5793(03)01076-7.

Abstract

Malate dehydrogenase (MDH) from the moderately thermophilic bacterium Chloroflexus aurantiacus (CaMDH) is a tetrameric enzyme, while MDHs from mesophilic bacteria usually are dimers. Using site-directed mutagenesis, we show here that a network of electrostatic interactions across the extra dimer-dimer interface in CaMDH is important for thermal stability and oligomeric integrity. Stability effects of single point mutations (E25Q, E25K, D56N, D56K) varied from -1.2 degrees C to -26.8 degrees C, and depended strongly on pH. Gel-filtration experiments indicated that the 26.8 degrees C loss in stability observed for the D56K mutant at low pH was accompanied by a shift towards a lower oligomerization state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Bacterial Proteins / chemistry*
  • Chlorobi / enzymology
  • Chromatography, Gel
  • Dimerization
  • Enzyme Stability
  • Hot Temperature
  • Hydrogen-Ion Concentration
  • Malate Dehydrogenase / chemistry*
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Protein Conformation
  • Protein Denaturation
  • Protein Structure, Quaternary
  • Protein Subunits
  • Recombinant Proteins / chemistry
  • Static Electricity
  • Temperature

Substances

  • Bacterial Proteins
  • Protein Subunits
  • Recombinant Proteins
  • Malate Dehydrogenase