Streptavidin-Hosted Organocatalytic Aldol Addition

Molecules. 2020 May 25;25(10):2457. doi: 10.3390/molecules25102457.

Abstract

In this report, the streptavidin-biotin technology was applied to enable organocatalytic aldol addition. By attaching pyrrolidine to the valeric motif of biotin and introducing it to streptavidin (Sav), a protein-based organocatalytic system was created, and the aldol addition of acetone with p-nitrobenzaldehyde was tested. The conversion of substrate to product can be as high as 93%. Although the observed enantioselectivity was only moderate (33:67 er), further protein engineering efforts can be included to improve the selectivity. These results have proven the concept that Sav can be used to host stereoselective aldol addition.

Keywords: aldol; artificial enzyme; biocompatible; catalysis; enamine; organocatalysis; protein; streptavidin.

MeSH terms

  • Acetone / chemistry
  • Aldehydes / chemistry*
  • Benzaldehydes / chemistry
  • Biotin / chemistry*
  • Chemistry Techniques, Synthetic*
  • Humans
  • Models, Molecular
  • Protein Conformation
  • Pyrrolidines / chemistry
  • Stereoisomerism
  • Streptavidin / chemistry*

Substances

  • Aldehydes
  • Benzaldehydes
  • Pyrrolidines
  • Acetone
  • 4-nitrobenzaldehyde
  • Biotin
  • 3-hydroxybutanal
  • Streptavidin
  • pyrrolidine