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  2. The human Krebs cycle 2-oxoglutarate dehydrogenase complex creates an additional source of superoxide/hydrogen peroxide from 2-oxoadipate as alternative substrate

The human Krebs cycle 2-oxoglutarate dehydrogenase complex creates an additional source of superoxide/hydrogen peroxide from 2-oxoadipate as alternative substrate

  • Free Radic Biol Med. 2017 Jul;108:644-654. doi: 10.1016/j.freeradbiomed.2017.04.017.
Natalia S Nemeria 1 Gary Gerfen 2 Elena Guevara 3 Pradeep Reddy Nareddy 3 Michal Szostak 3 Frank Jordan 4
Affiliations

Affiliations

  • 1 Department of Chemistry, Rutgers University, Newark, NJ 07102-1811, USA. Electronic address: nemeria@newark.rutgers.edu.
  • 2 Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, NY 10461-2304, USA. Electronic address: gary.gerfen@einstein.yu.edu.
  • 3 Department of Chemistry, Rutgers University, Newark, NJ 07102-1811, USA.
  • 4 Department of Chemistry, Rutgers University, Newark, NJ 07102-1811, USA. Electronic address: frjordan@newark.rutgers.edu.
Abstract

Recently, we reported that the human 2-oxoglutarate dehydrogenase (hE1o) component of the 2-oxoglutarate dehydrogenase complex (OGDHc) could produce the Reactive Oxygen Species superoxide and hydrogen peroxide (detected by chemical means) from its substrate 2-oxoglutarate (OG), most likely concurrently with one-electron oxidation by dioxygen of the thiamin diphosphate (ThDP)-derived enamine intermediate to a C2α-centered radical (detected by Electron Paramagnetic Resonance) [Nemeria et al., 2014 [17]; Ambrus et al. 2015 [18]]. We here report that hE1o can also utilize the next higher homologue of OG, 2-oxoadipate (OA) as a substrate according to multiple criteria in our toolbox: (i) Both E1o-specific and overall complex activities (NADH production) were detected using OA as a substrate; (ii) Two post-decarboxylation intermediates were formed by hE1o from OA, the ThDP-enamine and the C2α-hydroxyalkyl-ThDP, with nearly identical rates for OG and OA; (iii) Both OG and OA could reductively acylate lipoyl domain created from dihydrolipoyl succinyltransferase (E2o); (iv) Both OG and OA gave α-ketol carboligaton products with glyoxylate, but with opposite chirality; a finding that could be of utility in chiral synthesis; (v) Dioxygen could oxidize the ThDP-derived enamine from both OG and OA, leading to ThDP-enamine radical and generation of superoxide and H2O2. While the observed oxidation-reduction with dioxygen is only a side reaction of the predominant physiological product glutaryl-CoA, the efficiency of superoxide/ H2O2 production was 7-times larger from OA than from OG, making the reaction of OGDHc with OA one of the important superoxide/ H2O2 producers among 2-oxo acid dehydrogenase complexes in mitochondria.

Keywords

2-oxoadipate; 2-oxoglutarate dehydrogenase; 2-oxoglutarate dehydrogenase complex; EPR; Superoxide and H(2)O(2) generation; ThDP-enamine radical; α-ketol carboligaton products.

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