In situ regeneration of NADH via lipoamide dehydrogenase-catalyzed electron transfer reaction evidenced by spectroelectrochemistry

Bioelectrochemistry. 2012 Aug:86:92-6. doi: 10.1016/j.bioelechem.2012.03.002. Epub 2012 Mar 27.

Abstract

NAD/NADH is a coenzyme found in all living cells, carrying electrons from one reaction to another. We report on characterizations of in situ regeneration of NADH via lipoamide dehydrogenase (LD)-catalyzed electron transfer reaction to regenerate NADH using UV-vis spectroelectrochemistry. The Michaelis-Menten constant (K(m)) and maximum velocity (V(max)) of NADH regeneration were measured as 0.80±0.15 mM and 1.91±0.09 μM s(-1) in a 1-mm thin-layer spectroelectrochemical cell using gold gauze as the working electrode at the applied potential -0.75 V (vs. Ag/AgCl). The electrocatalytic reduction of the NAD system was further coupled with the enzymatic conversion of pyruvate to lactate by lactate dehydrogenase to examine the coenzymatic activity of the regenerated NADH. Although the reproducible electrocatalytic reduction of NAD into NADH is known to be difficult compared to the electrocatalytic oxidation of NADH, our spectroelectrochemical results indicate that the in situ regeneration of NADH via LD-catalyzed electron transfer reaction is fast and sustainable and can be potentially applied to many NAD/NADH-dependent enzyme systems.

Publication types

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

MeSH terms

  • Dihydrolipoamide Dehydrogenase / chemistry
  • Dihydrolipoamide Dehydrogenase / metabolism*
  • Electrochemical Techniques
  • Electrodes
  • Electron Transport
  • Lactates / chemistry
  • Lactates / metabolism
  • NAD / chemistry
  • NAD / metabolism*
  • Pyruvic Acid / chemistry
  • Pyruvic Acid / metabolism
  • Spectrophotometry, Ultraviolet / instrumentation
  • Spectrophotometry, Ultraviolet / methods*

Substances

  • Lactates
  • NAD
  • Pyruvic Acid
  • Dihydrolipoamide Dehydrogenase