Functional analysis of a mosquito short-chain dehydrogenase cluster

Arch Insect Biochem Physiol. 2013 Feb;82(2):96-115. doi: 10.1002/arch.21078. Epub 2012 Dec 13.

Abstract

The short-chain dehydrogenases (SDR) constitute one of the oldest and largest families of enzymes with over 46,000 members in sequence databases. About 25% of all known dehydrogenases belong to the SDR family. SDR enzymes have critical roles in lipid, amino acid, carbohydrate, hormone, and xenobiotic metabolism as well as in redox sensor mechanisms. This family is present in archaea, bacteria, and eukaryota, emphasizing their versatility and fundamental importance for metabolic processes. We identified a cluster of eight SDRs in the mosquito Aedes aegypti (AaSDRs). Members of the cluster differ in tissue specificity and developmental expression. Heterologous expression produced recombinant proteins that had diverse substrate specificities, but distinct from the conventional insect alcohol (ethanol) dehydrogenases. They are all NADP⁺-dependent and they have S-enantioselectivity and preference for secondary alcohols with 8-15 carbons. Homology modeling was used to build the structure of AaSDR1 and two additional cluster members. The computational study helped explain the selectivity toward the (10S)-isomers as well as the reduced activity of AaSDR4 and AaSDR9 for longer isoprenoid substrates. Similar clusters of SDRs are present in other species of insects, suggesting similar selection mechanisms causing duplication and diversification of this family of enzymes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aedes / chemistry
  • Aedes / enzymology*
  • Amino Acid Sequence
  • Animals
  • Computational Biology
  • Gene Expression Regulation
  • Insect Proteins / chemistry
  • Insect Proteins / metabolism*
  • Molecular Docking Simulation
  • Organ Specificity
  • Oxidoreductases / chemistry
  • Oxidoreductases / metabolism*
  • Phylogeny
  • Polymerase Chain Reaction
  • RNA / metabolism
  • Sequence Alignment
  • Spectrophotometry
  • Substrate Specificity

Substances

  • Insect Proteins
  • RNA
  • Oxidoreductases