Benzaldehyde lyase, a novel thiamine PPi-requiring enzyme, from Pseudomonas fluorescens biovar I

J Bacteriol. 1989 May;171(5):2401-5. doi: 10.1128/jb.171.5.2401-2405.1989.

Abstract

Pseudomonas fluorescens biovar I can grow on benzoin as the sole carbon and energy source. This ability is due to benzaldehyde lyase, a new type of enzyme that irreversibly cleaves the acyloin linkage of benzoin, producing two molecules of benzaldehyde. Benzaldehyde lyase was purified 70-fold and found to require catalytic amounts of thiamine PPi (TPP) and a divalent cation as cofactors. Optimal activity was obtained with a 1.0 mM concentration of Mn2+, Mg2+, or Ca2+. Gel permeation chromatography indicated a native molecular weight of 80,000, whereas the enzyme migrated in sodium dodecyl sulfate-containing polyacrylamide gels as a single polypeptide with a molecular weight of 53,000. Benzaldehyde lyase is highly specific; of a variety of structurally related compounds tested, only benzoin and anisoin (4,4'-dimethoxybenzoin) acted as substrates, their apparent Kms being 9.0 x 10(-3) and 3.25 x 10(-2) mM, respectively. A catalytic mechanism for the enzyme is proposed.

Publication types

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

MeSH terms

  • Aldehyde-Lyases / isolation & purification
  • Aldehyde-Lyases / metabolism*
  • Benzaldehydes / metabolism*
  • Benzoin / metabolism
  • Catalysis
  • Cations, Divalent / metabolism
  • Molecular Weight
  • Pseudomonas fluorescens / enzymology*
  • Substrate Specificity
  • Thiamine Pyrophosphate / metabolism*

Substances

  • Benzaldehydes
  • Cations, Divalent
  • Aldehyde-Lyases
  • benzaldehyde lyase
  • Benzoin
  • Thiamine Pyrophosphate