CINNAMIC ACID HYDROXYLASE IN SPINACH,

Abstract

An acetone precipitate from an extract of spinach leaves catalysed the hydroxylation of trans-cinnamic acid to p-coumaric acid. The enzyme was unstable and could not be purified. Crude preparations had a pH optimum of 4.6 and showed an absolute requirement for an external electron donor. Tetrahydrofolic acid and a reduced pyridine nucleotide coenzyme were necessary for maximum activity. Aminopterin was a potent inhibitor of the hydroxylating system. No requirement for metal ions could be demonstrated but inhibition by p-chloromercuribenzoate suggests that a sulfhydryl group participates in the reaction. These properties, and the course of the reaction when cofactors were added separately, indicate a similarity between this enzyme and the phenylalanine hydroxylase of mammalian liver. The crude spinach preparation also catalysed and the conversion of L-phenylalanine to tyrosine, and addition of L-phenylalanine inhibited cinnamic acid hydroxylase activity. (Author)

Document Details

Document Type
Technical Report
Publication Date
May 21, 1964
Accession Number
AD0618160

Entities

People

  • L. C. Vining
  • P. M. Nair

Organizations

  • National Research Council Canada

Tags

DTIC Thesaurus Topics

  • Acids
  • Biomolecules
  • Chemical Compounds
  • Cinnamic Acid
  • Coenzymes
  • Conversion
  • Electron Donors
  • Electrons
  • Inhibition
  • Inhibitors
  • Nucleotides
  • Phenylalanine
  • Precipitates
  • Pyridines

Fields of Study

  • Biology

Readers

  • Analytical Chemistry
  • Molecular and Cellular Biochemistry

Technology Areas

  • Microelectronics