Analysis of Degradation Pathways from Cinnamic Acid to Acetophenone by Mucor sp.
DOI:
CSTR:
Author:
Affiliation:

Clc Number:

O652.1

Fund Project:

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    The metabolic pathway for the degradation of cinnamic acid with Mucor sp. was studied by analyzing metabolites using GC-MS. β-phenethyl alcohol, for the first time, was detected as an intermediate in transforming cinnamic acid to acetophenone by Mucor sp. The metabolic pathway of cinnamic acid was supposed: epoxidation reaction was occurred on the double bond of cinnamic acid side chain to generate ethyl 2,3-epoxy-3-phenylpropionic acid, the epoxide was converted to β-phenethyl alcohol via decarboxylation and ring-opening reaction, lastly, acetophenone was produced from β-phenethyl alcohol via hydroxyl migration and oxidation reaction.

    Reference
    Related
    Cited by
Get Citation
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:November 20,2012
  • Revised:December 27,2012
  • Adopted:January 24,2013
  • Online: March 26,2013
  • Published:
Article QR Code