Chemoenzymatic Preparation of 4'-Thioribose NAD

Curr Protoc Nucleic Acid Chem. 2019 Jun;77(1):e83. doi: 10.1002/cpnc.83. Epub 2019 Apr 5.

Abstract

This chemoenzymatic procedure describes a strategy for the preparation of 4'-thioribose nicotinamide adenine dinucleotide (S-NAD+ ), including chemical synthesis of nicotinamide 4'-riboside (S-NR), recombinant expression and purification of two NAD+ biosynthesis enzymes nicotinamide riboside kinase (NRK) and nicotinamide mononucleotide adenylyltransferase (NMNAT), and enzymatic synthesis of S-NAD+ . The first basic protocol describes the procedures for introduction of nicotinamide onto 4'-thioribose and subsequent deprotection to generate S-NR as the key intermediate for enzymatically synthesizing S-NAD+ . In the second basic protocol, experimental methods are detailed for the production of recombinant human NRK1 and NMNAT1 to catalyze conversion of S-NR to S-NAD+ . The third basic protocol presents the enzymatic approach for the generation of S-NAD+ from S-NR precursor. © 2019 by John Wiley & Sons, Inc.

Keywords: 4′-thioribose; NAD+; NMNAT; NRK; chemoenzymatic synthesis; nicotinamide riboside.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cloning, Molecular
  • Escherichia coli / genetics
  • Humans
  • NAD / chemical synthesis*
  • NAD / chemistry
  • Nicotinamide-Nucleotide Adenylyltransferase / chemistry*
  • Nicotinamide-Nucleotide Adenylyltransferase / genetics
  • Nicotinamide-Nucleotide Adenylyltransferase / isolation & purification
  • Phosphotransferases (Alcohol Group Acceptor) / chemistry*
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • Phosphotransferases (Alcohol Group Acceptor) / isolation & purification
  • Ribose / chemistry*
  • Sulfhydryl Compounds / chemistry*

Substances

  • Sulfhydryl Compounds
  • NAD
  • Ribose
  • Phosphotransferases (Alcohol Group Acceptor)
  • NMRK1 protein, human
  • NMNAT1 protein, human
  • Nicotinamide-Nucleotide Adenylyltransferase