Oxidation of NADH

Oxidation of P-nicotinamide adenine dinucleotide (NADH) to NAD+ has attracted much interest from the viewpoint of its role in biosensors reactions. It has been reported that several quinone derivatives and polymerized redox dyes, such as phenoxazine and phenothiazine derivatives, possess catalytic activities for the oxidation of NADH and have been used for dehydrogenase biosensors development [1, 2]. Flavins (contain in chemical structure isoalloxazine ring) are the prosthetic groups responsible for NAD+/NADH conversion in the active sites of some dehydrogenase enzymes. Upon the electropolymerization of flavin derivatives, the effective catalysts of NAD+/NADH regeneration, which mimic the NADH-dehydrogenase activity, would be synthesized [3]. 

The half-reactions and reduction potentials in Table 21.1 can be used to analyze energy changes in redox reactions. The oxidation of NADH to NAD can be coupled with the reduction of a-ketoglutarate to isocitrate ... 

FIGURE 21.33 The glycerophosphate shuttle (also known as the glycerol phosphate shuttle) couples the cytosolic oxidation of NADH with mitochondrial reduction of [FAD]. 

Note The.se P/O ratios of 2.5 and 1.5 for mitochondrial oxidation of NADH and [FADHg] are consen.sns values. Because diey may not reflect actual values and because these ratios may change depending on metabolic conditions, the.se estimates of ATP yield from glucose oxidation are approximate. 

Consider the oxidation of NADH by molecular oxygen as carried out via the electron transport pathway... 

During dtric add production there is massive generation of NADH but little demand for ATP. Thus the situation could quickly arise where there is no further ADP available for oxidative phosphorylation within the cells. This means that the electron transport chain cannot operate and no further oxidation of NADH can occur. 

To circumvent high overvoltage and fouling problems encountered with the direct oxidation of NADH at conventional electrode (equation 6-11), much work has been devoted to the development of modified electrodes with catalytic properties for... 

CK catalyzes the reversible phosphorylation of creatine in the presence of ATP and magnesium. When creatine phosphate is the substrate, the resulting creatine can be measured as the ninhydrin fluorescent compound, as in the continuous flow Auto Analyzer method. Kinetic methods based on coupled enzymatic reactions are also popular. Tanzer and Gilvarg (40) developed a kinetic method using the two exogenous enzymes pyruvate kinase and lactate dehydrogenase to measure the CK rate by following the oxidation of NADH. In this procedure the main reaction is run in a less favorable direction. 

Many dehydrogenase enzymes catalyze oxidation/reduction reactions with the aid of nicotinamide cofactors. The electrochemical oxidation of nicotinamide adeniiw dinucleotide, NADH, has been studied in depthThe direct oxidation of NADH has been used to determine concentration of ethanol i s-isv, i62) lactate 157,160,162,163) pyTuvate 1 ), glucose-6-phosphate lactate dehydrogenase 159,161) alanine The direct oxidation often entails such complications as electrode surface pretreatment, interferences due to electrode operation at very positive potentials, and electrode fouling due to adsorption. Subsequent reaction of the NADH with peroxidase allows quantitation via the well established Clark electrode. 

Ferricyanide has been employed as an electron acceptor for lactate in place of NAD Alternatively, diaphorase can be used in conjunction with ferricyanide Bindschedler s Green ferricenium or dichlorophenylindophenol to catalyze the oxidation of NADH while providing a more easily monitored species than NADH itself. 

The famous model for the oxidation of NADH coupled with the proton transport in a mitochondria is the Q cycle [53], as follows NADH in the aqueous solution (matrix) is oxidized to NAD by Q in the membrane producing hydroquinone (QH2). 

Taking into account the results obtained by polarography as well as controlled potential electrolysis, the reaction which proceeded in Range A and gave the polarographic wave was estimated to be composed of two-electron oxidation of NADH and one-electron reduction of CQ at the W/DCE interface. The oxidation of NADH is accompanied by the dissociation of one H in W. 

The reaction in Range B did not give any polarographic currents but produced NAD and CQH2. Hence, the reaction was estimated to be two-electron oxidation of NADH by CQ accompanied by two-H transfer at the W/DCE interface,... 

As dehydrogenases (DH) are widely distributed enzymes, a number of studies have been carried out with these biocatalysts. For example, Willner el al. [20] have used a PQQ-monolayer functionalized gold electrode for the catalytic oxidation of NADH in the presence of Ca2+. In this scheme, the pyrrolo-quinoline quinine co-factor, PQQ, was covalently linked, as before for the GOx system [15, 20, 21], to the Au electrode,... 

Simon et al. [92] investigated a biocatalytic anode based on lactate oxidation by lactate dehydrogenase (LDH). The anodic current is generated by the oxidation of NADH (produced by NAD+ and substrate) while LDH catalyzes the electro-oxidation of lactate into pyruvate. As previously mentioned, the oxidation of NADH at bare electrodes requires a large overpotential, so these authors used poly(aniline) films doped with polyanions to catalyze NADH oxidation. Subsequent research by this group focused on targeting mutants of LDH that are amenable to immobilization on the polyaniline surface [93],... 

Ten years ago oxidation of NADH [84, 85] seems not to be important because of the other more powerful electrocatalysts [86-89], A possibility for oxidation of guanine even in DNA [90] with cobalt hexacyanoferrate, on the contrary, seems to be more apposite. 

C.X. Cai, H.X. Ju, and H.Y. Chen, Cobalt hexacyanoferrate-modified microband gold electrode and its electrocatalytic activity for oxidation of NADH. J. Electroanal. Chem. 397,185-190 (1995). 

Xanthothricin 308 stimulated oxidation of NADH and NAD-linked substrates by rat liver mitochondria, yeast mitochondria, and Ehrlich ascites tumor cells (74MI1, 74MI3). It also stimulated mitochondrial oxidation of succinate, pyruvate, or malate. The antibiotic xanthothricin was obtained... 

The P/O ratio is the number of ATPs made for each O atom consumed by mitochondrial respiration. The P stands for high-energy phosphate equivalents, and the O actually stands for the number of I 02 s that are consumed by the electron transport chain. The full reduction of 02 to 2 H20 takes 4 electrons. Therefore, 2 electrons reduce of an 02. The oxidation of NADH to NAD and the oxidation of FADH2 to FAD are both 2-electron oxidations. O can be read as the transfer of 2 electrons. It s not quite as obscure as it sounds.2... 

In the presence of the inhibitor rotenone (to prevent the oxidation of NADH by the electron transport chain), succinate can be metabolized only to fumarate, producing an FADH2 in the process. 

Rotenone NADH-CoQ reductase Blocks oxidation of NADH (site I). NADH will become reduced Substrates such as succinate that enter via FADH will still be oxidized and make 2 ATPs/mol. 

Peroxynitrite reacts with heme proteins such as prostacycline synthase (PGI2), microperoxidase, and the heme thiolate protein P450 to form a ferryl nitrogen dioxide complex as an intermediate [120]. Peroxynitrite also reacts with acetaldehyde with the rate constant of 680 1 mol 1 s" 1 forming a hypothetical adduct, which is decomposed into acetate, formate, and methyl radicals [121]. The oxidation of NADH and NADPH by peroxynitrite most certainly occurs by free radical mechanism [122,123], Kirsch and de Groot [122] concluded that peroxynitrite oxidized NADH by a one-electron transfer mechanism to form NAD and superoxide ... 

Because the direct electrochemical oxidation of NAD(P)H has to take place at an anode potential of + 900 mV vs NHE or more, only rather oxidation-stable substrates can be transformed without loss of selectivity—thus limiting the applicability of this method. The electron transfer between NADH and the anode may be accellerated by the use of a mediator. At the same time, electrode fouling which is often observed in the anodic oxidation of NADH can be prevented. Synthetic applications have been described for the oxidation of 2-hexene-l-ol and 2-butanol to 2-hexenal and 2-butanone catalyzed by yeast alcohol dehydrogenase (YADH) and the alcohol dehydrogenase from Thermoanaerobium brockii (TBADH) repectively with indirect electrochemical... 

---