Improved one-pot multienzyme (OPME) systems for synthesizing UDP-uronic acids and glucuronides

Chem Commun (Camb). 2015 Mar 18;51(22):4595-8. doi: 10.1039/c4cc10306h.

Abstract

Arabidopsis thaliana glucuronokinase (AtGlcAK) was cloned and shown to be able to use various uronic acids as substrates to produce the corresponding uronic acid-1-phosphates. AtGlcAK or Bifidobacterium infantis galactokinase (BiGalK) was used with a UDP-sugar pyrophosphorylase, an inorganic pyrophosphatase, with or without a glycosyltransferase for highly efficient synthesis of UDP-uronic acids and glucuronides. These improved cost-effective one-pot multienzyme (OPME) systems avoid the use of nicotinamide adenine dinucleotide (NAD(+))-cofactor in dehydrogenase-dependent UDP-glucuronic acid production processes and can be broadly applied for synthesizing various glucuronic acid-containing molecules.

Publication types

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

MeSH terms

  • Adenosine Diphosphate / biosynthesis*
  • Adenosine Diphosphate / chemistry
  • Arabidopsis / enzymology
  • Bifidobacterium / enzymology
  • Carbohydrate Conformation
  • Carbohydrate Sequence
  • Glucuronides / biosynthesis*
  • Glucuronides / chemistry
  • Molecular Sequence Data
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism*
  • Uronic Acids / chemistry
  • Uronic Acids / metabolism*

Substances

  • Glucuronides
  • Uronic Acids
  • Adenosine Diphosphate
  • Phosphotransferases (Alcohol Group Acceptor)
  • glucuronokinase