ETF = Electron-transferring flavoprotein

FeS Iron-sulfur protein ETF Electron-transferring flavoprotein Ep Elavoprotein Q Ubiquinone Cyt Cytochrome... 

Table 3.2.5 Disorders detectable by the in vitro probe assay. ETF Electron transfer flavoprotein, MADD multiple acyl-CoA dehydrogenase deficiency...

Fig. 5.2. Possible metabolic pathways in facultative anaerobic mitochondria. Shaded boxes show components of the electron-transport chain used during hypoxia, open boxes are components used during aerobiosis, and the hatched boxes (complex I and ATP-synthase) are components used under aerobic as well as anaerobic conditions. ASCT acetate succinate CoA-transferase, C cytochrome c, Cl, CIII and CIV complexes I, III and IV of the respiratory chain, CITR citrate, ECR enoyl-CoA reductase (such as present in Ascaris suum), ETF electron-transfer flavoprotein, ETF RQ OR electron-transfer flavoproteimrhodoquinone oxidoreductase, FRD fumarate reductase, FUM fumarate, MAE malate, OXAC oxaloacetate, PYR pyruvate, RQ rhodoquinone, SDH succinate dehydrogenase, SUCC succinate, Succ-CoA succinyl-CoA, TER trans-2-enoyl-CoA reductase (such as present in E. gracilis), UQ ubiquinone...

Figure 17.4 The electron transport chain of mitochondria. Triangles indicate sites of inhibition by various compounds. Cyt, cytochrome ETF, electron transfer flavoprotein. (Reproduced with permission from Moreadith RW, Batshaw ML, Ohnishi T, Kerr D, Knox B, Jackson D, Hruben R, Olson J, Reynafarje B, Lehninger AL. Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis J Clin Invest 74 685-697, 1984.)...

I and n are membrane-associated carnityl transferases ETF = electron transferring flavoprotein FP = flavoprotein... 

GTP = 5 -guanosine triphosphate AE = Activating enzyme BAN = Backbone amide nitrogen BioB = Biotin synthase CD = Circular dichroism cyt = Cytochrome DFT = Density functional theory DMSO = Dimethylsulfoxide Dx = Desulforedoxin ENDOR = Electron-nuclear double resonance EPR = Electron paramagnetic resonance ESEEM = Electron-spin echo envelop modulation ETF = Electron transferring flavoprotein EXAFS = Extended x-ray absorption fine structure FAD = Flavin adenine dinucleotide Fd = Ferredoxin FMN = Flavin mononucleotide FNR = Fumarate-nitrate reduction FTIR =... 

In addition to NADH dehydrogenase, succinic dehydrogenase and other flavopro-teins in the inner mitochondrial membrane also pass electrons to CoQ (see Fig. 21.5). Succinate dehydrogenase is part of the TCA cycle. ETF-CoQ oxidore-ductase accepts electrons from ETF (electron transferring flavoprotein), which acquires them from fatty acid oxidation and other pathways. Both of these flavo-proteins have Fe-S centers. a-Glycerophosphate dehydrogenase is a flavoprotein that is part of a shuttle for reoxidizing cytosolic NADH. 

Fig. 23.8. Transfer of electrons from acyl CoA dehydrogenase to the electron transport chain. Abbreviations ETF, electron-transferring flavoprotein ETF-QO, electron-transferring flavoprotein-Coenzyme Q oxidoreductase.

FIGURE 9.2 Physiology of ABE fermentation metabolism of Clostridium acetobutylicum with the respective enzymes and products. CoA, coenzyme A Ldh, lactate dehydrogenase Pdc, pyruvate decarboxylase Pfor, pyruvate ferredoxin oxidoreductase Fdred, ferredoxin reduced Thl, thiolase Hbd, p-hydroxybutyryl-CoA dehydrogenase Crt, crotonase Bed, butyryl-CoA dehydrogenase Etf, electron transfer flavoprotein Pta, phosphotransacetylase Ack, acetate kinase Ptb, phosphotransbutyrylase Buk, butyrate kinase Ctf A/B, acetoacetyl-CoA acyl-CoA transferase Adc, acetoacetate decarboxylase AdhE, aldehyde/alcohol dehydrogenase Bdh, butanol dehydrogenase. 

The oxidation of fatty acids is catalyzed by the FAD-containing acyl coenzyme A dehydrogenases which transfer reducing equivalents to the mitochondrial respiratory chain via a flavin-containing electron transfer flavoprotein (ETF) and subsequently via an ETF dehydrogenase (an Fe/S flavoprotein In addition to the mammalian... 

As described before, also the formation of branched-chain fatty acids by enoyl-CoA reductase activity is coupled to electron transport (Komuniecki and Harris 1995). In this case electrons are transported from NADH to rhodoquinone via complex I and subsequently to the electron-transfer flavoprotein (ETF) via ETF-reductase (Fig. 5.3). The soluble, non-membrane-bound ETF then transfers electrons to enoyl-CoA reductase, which uses the electrons for the condensation of two short-chain (C2-C3) acyl-CoA moieties for the formation of branched-chain fatty acids. 

Figure 18.5 The glycerol-3-phosphate shuttle. This shuttle is used to bring electrons from cytosolic NADH into mitochondria. The mitochondrial glycerol-3-phosphate dehydrogenase with its FAD prosthetic group is bound to the inner mitochondrial membrane. ETF is electron transfer flavoprotein, which extracts electrons from the FADH2 of mitochondrial glycerol-3-phosphate dehydrogenase and with it reduces ubiquinone (UQ).

A distinct electron transfer flavoprotein (ETF) is the single-electron acceptor for a variety of flavoprotein dehydrogenases, including acyl CoA, glutaryl CoA, sarcosine, and dimethylglycine dehydrogenases. It then transfers the electrons to ETF-ubiquinone reductase, the iron-sulfur flavoprotein that reduces ubiquinone in the mitochondrial electron transport chain. 

The mitochondrial respiratory chain, which contains at least 13 Fe-S clusters (Figure 6), perhaps best illustrates the importance of Fe-S clusters in membrane-bound electron transport. Electrons enter via three principal pathways, from the oxidation of NADH to NAD+ (NADH-ubiquinone oxidoreductase or Complex I) and succinate to fumarate (succinate ubiquinone oxidoreductase or Complex II), and from the /3-oxidation of fatty acids via the electron transferring flavoprotein (ETF-ubiquinone oxidoreductase). All three pathways involve a complex Fe S flavoprotein dehydrogenase, that is, NADH dehydrogenase, succinate dehydrogenase, and ETF dehydrogenase, and in each case the Fe-S clusters mediate electron transfer from the flavin active site to the ubiquinone pool via protein-associated ubiquinone. 

Fig. 3.1. A, The respiratory chain. Q and c stand for ubiquinone and cytochrome c, respectively. Auxiliary enzymes that reduce ubiquinone include succinate dehydrogenase (Complex II), a-glycerophosphate dehydrogenase and the electron-transferring flavoprotein (ETF) of fatty acid oxidation. Auxiliary enzymes that reduce cytochrome c include sulphite oxidase. B, Thermodynamic view of the respiratory chain in the resting state (State 4). Approximate values are calculated according to the Nernst equation using oxidoreduction states from work by Muraoka and Slater, (NAD, Q, cytochromes c c, and a oxidation of succinate [6]), and Wilson and Erecinska (b-562 and b-566 [7]). The NAD, Q, cytochrome b-562 and oxygen/water couples are assumed to equilibrate protonically with the M phase at pH 8 [7,8]. E j (A ,/ApH) for NAD, Q, 6-562, and oxygen/water are taken as —320 mV ( — 30 mV/pH), 66 mV (- 60 mV/pH), 40 mV (- 60 mV/pH), and 800 mV (- 60 mV/pH) [7-10]. FMN and the FeS centres of Complex I (except N-2) are assumed to be in redox equilibrium with the NAD/NADH couple, FeS(N-2) with ubiquinone [11], and cytochrome c, and the Rieske FeS centre with cytochrome c [10]. The position of cytochrome a in the figure stems from its redox state [6] and its apparent effective E -, 285 mV in...

Figure 8. ESR (upper) and ENDOR (lower) spectra from flavoproteins at — 160°C. a, Semiquinone radicals from the one-electron reduction of electron-transfer flavoprotein (ETF) b, semiquinone radicals from the one-electron reduction of sarcosine dehydrogenase. From [144], with permission.

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