Purification and characterization of a new aldehyde oxidase from pseudomonas sp. AIU 362

J Biosci Bioeng. 2008 Sep;106(3):297-302. doi: 10.1263/jbb.106.297.

Abstract

An aldehyde oxidase exhibiting high activity on glyoxal was purified to an electrophoretically homogenous state from Pseudomonas sp. AIU 362, which was isolated from a soil sample using a methoxyethanol medium. The enzyme oxidized not only glyoxal but also short-chain aliphatic aldehydes and aromatic aldehydes. Thus, this enzyme was classified into the aldehyde oxidase (ALOD) group. However, it was composed of four identical subunits with a molecular mass of 27 kDa, whereas other microbial ALODs were composed of three hetero subunits, and ALODs from plant and animals were composed of two identical subunits. The NH(2)-terminal sequence also showed no similarity to that of other ALODs. These results indicate that ALOD from Pseudomonas sp. AIU 362 is a new aldehyde oxidase. This ALOD was induced by 2-methoxyethanol, methanol or isopropanol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Oxidase / chemistry*
  • Aldehyde Oxidase / isolation & purification*
  • Amino Acid Sequence
  • Enzyme Activation
  • Enzyme Stability
  • Molecular Sequence Data
  • Molecular Weight
  • Pseudomonas / classification*
  • Pseudomonas / enzymology*
  • Soil Microbiology*
  • Species Specificity

Substances

  • Aldehyde Oxidase