Purification and characterization of a carbohydrate: acceptor oxidoreductase from Paraconiothyrium sp. that produces lactobionic acid efficiently

Biosci Biotechnol Biochem. 2008 Mar;72(3):833-41. doi: 10.1271/bbb.70701. Epub 2008 Mar 7.

Abstract

A carbohydrate:acceptor oxidoreductase from Paraconiothyrium sp. was purified and characterized. The enzyme efficiently oxidized beta-(1-->4) linked sugars, such as lactose, xylobiose, and cellooligosaccharides. The enzyme also oxidized maltooligosaccharides, D-glucose, D-xylose, D-galactose, L-arabinose, and 6-deoxy-D-glucose. It specifically oxidized the beta-anomer of lactose. Molecular oxygen and 2,6-dichlorophenol indophenol were reduced by the enzyme as electron acceptors. The Paraconiothyrium enzyme was identified as a carbohydrate:acceptor oxidoreductase according to its specificity for electron donors and acceptors, and its molecular properties, as well as the N-terminal amino acid sequence. Further comparison of the amino acid sequences of lactose oxidizing enzymes indicated that carbohydrate:acceptor oxidoreductases belong to the same group as glucooligosaccharide oxidase, while they differ from cellobiose dehydrogenases and cellobiose:quinone oxidoreductases.

MeSH terms

  • Alcohol Oxidoreductases
  • Carbohydrate Dehydrogenases / isolation & purification*
  • Carbohydrate Dehydrogenases / metabolism*
  • Disaccharides / biosynthesis*
  • Enzyme Stability
  • Fungal Proteins / isolation & purification*
  • Fungal Proteins / metabolism
  • Lactose / metabolism*

Substances

  • Disaccharides
  • Fungal Proteins
  • lactobionic acid
  • Alcohol Oxidoreductases
  • Carbohydrate Dehydrogenases
  • glucooligosaccharide oxidase
  • Lactose