Heteronuclear NMR analysis of unsaturated fatty acids in poly(3-hydroxyalkanoates). Study of beta-oxidation in Pseudomonas putida

J Biol Chem. 1993 Jan 5;268(1):315-9.

Abstract

Poly(3-hydroxyalkanoates) (PHAs) were isolated from Pseudomonas putida KT2442 cultivated on petroselenic acid, oleic acid, and linoleic acid to study beta-oxidation of unsaturated fatty acids. Both saturated and unsaturated medium chain length 3-hydroxy fatty acids were found to be constituents of these polymers. With the aid of proton-detected multiple quantum coherence and proton-detected multiple bond coherence NMR spectra the structures of the unsaturated monomers were identified as 3-hydroxy-5-cis-tetradecanoate for PHA produced on oleic acid, and 3-hydroxy-6-cis-dodecanoate and 3-hydroxy-5-cis-8-cis-tetradecadienoate for PHA produced on linoleic acid. The identified structures, which are derived from fatty acid degradation intermediates, indicate a degradation of oleic acid via the enoyl-CoA isomerase-dependent route and a degradation of linoleic acid via the dienoyl-CoA reductase-dependent route.

MeSH terms

  • Carbon Isotopes
  • Fatty Acids, Nonesterified / chemistry
  • Fatty Acids, Nonesterified / isolation & purification
  • Fatty Acids, Nonesterified / metabolism*
  • Gas Chromatography-Mass Spectrometry
  • Hydrogen
  • Hydroxy Acids / chemistry
  • Hydroxy Acids / isolation & purification
  • Hydroxy Acids / metabolism*
  • Linoleic Acid
  • Linoleic Acids / metabolism
  • Magnetic Resonance Spectroscopy
  • Molecular Conformation
  • Oleic Acid
  • Oleic Acids / metabolism
  • Oxidation-Reduction
  • Pseudomonas putida / metabolism*

Substances

  • Carbon Isotopes
  • Fatty Acids, Nonesterified
  • Hydroxy Acids
  • Linoleic Acids
  • Oleic Acids
  • Oleic Acid
  • petroselinic acid
  • Hydrogen
  • Linoleic Acid