Light-Driven Enzymatic Decarboxylation of Dicarboxylic Acids

ChemistryOpen. 2021 May;10(5):553-559. doi: 10.1002/open.202100039.

Abstract

Photodecarboxylase from Chlorella variabillis (CvFAP) is one of the three known light-activated enzymes that catalyzes the decarboxylation of fatty acids into the corresponding C1-shortened alkanes. Although the substrate scope of CvFAP has been altered by protein engineering and decoy molecules, it is still limited to mono-fatty acids. Our studies demonstrate for the first time that long chain dicarboxylic acids can be converted by CvFAP. Notably, the conversion of dicarboxylic acids to alkanes still represents a chemically very challenging reaction. Herein, the light-driven enzymatic decarboxylation of dicarboxylic acids to the corresponding (C2-shortened) alkanes using CvFAP is described. A series of dicarboxylic acids is decarboxylated into alkanes in good yields by means of this approach, even for the preparative scales. Reaction pathway studies show that mono-fatty acids are formed as the intermediate products before the final release of C2-shortened alkanes. In addition, the thermostability, storage stability, and recyclability of CvFAP for decarboxylation of dicarboxylic acids are well evaluated. These results represent an advancement over the current state-of-the-art.

Keywords: alkanes; biodegradable plastic; decarboxylation; dicarboxylic acids; photobiocatalysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkanes / chemistry
  • Biocatalysis
  • Biodegradable Plastics / chemistry
  • Carboxy-Lyases / metabolism*
  • Catalytic Domain
  • Chlorella / enzymology*
  • Decarboxylation
  • Dicarboxylic Acids / chemistry*
  • Fatty Acids / chemistry
  • Light
  • Molecular Docking Simulation
  • Photochemical Processes
  • Protein Binding
  • Protein Engineering
  • Structure-Activity Relationship

Substances

  • Alkanes
  • Biodegradable Plastics
  • Dicarboxylic Acids
  • Fatty Acids
  • Carboxy-Lyases