Kinetic mechanisms of electron bifurcation with electron transfer flavoprotein, NADH, butyryl-CoA dehydrogenase, and ferredoxin reveal a semiquinone cycle

Abstract

Electron transfer flavoprotein (EtfAB, with α-FAD and β-FAD) and tetrameric butyryl-CoA dehydrogenase (Bcd, with δ-FAD in each subunit) from Acidaminococcus fermentans catalyze electron bifurcation which reduces low potential ferredoxin (Fd) and high potential crotonyl-CoA using NADH as an electron donor. Our previous rapid kinetic studies have demonstrated “pseudo-electron bifurcation” where NADH and two EtfAB molecules generate EtfA<inf>SQ</inf>B (A<inf>SQ</inf> contains α-FAD^•−) and the charge-transfer complex of EtfA<inf>SQ</inf>B<inf>HQ</inf>:NAD⁺ (B<inf>HQ</inf> contains β-FADH⁻). Since the radical in EtfA<inf>SQ</inf>B inhibits the further reduction of β-FAD with NADH, the question arises as to how the five components of the complete system interact to mediate the whole flavin-based electron bifurcation. This study shows that Bcd releases the inhibition effect of α-FAD^•−, allowing fast β-FAD reduction for turnover. In the presence of both Bcd and Fd, the total β-FADH⁻ of EtfAB bifurcates to afford α-FAD^•− and Fd⁻; a second bifurcation yields α-FADH⁻ in the Bcd-EtfA<inf>HQ</inf>B complex and additional Fd⁻. In the presence of crotonyl-CoA, two simultaneous one-electron transfers from both EtfA<inf>HQ</inf>B yield reduced Bcd and two EtfA<inf>SQ</inf>B, confirmed by electron paramagnetic resonance spectroscopy. This step is proposed to require a slow conformational change of the Bcd-EtfAB complex for electron transfer with a limiting rate constant of 0.0098 s⁻¹ at 4 °C, but increases about 14-fold to 0.14 s⁻¹ at 30 °C, the optimal growth temperature of A. fermentans. The final reduction of crotonyl-CoA to butyryl-CoA completes the cycle, which we call the semiquinone cycle of electron bifurcation, because it starts and ends with a semiquinone.