The re-oxidation generated a total of 239 μM free thiol groups GF120918 ic50 in this representative experiment, a result that is in approximate agreement with the observed oxidation of 106 μM 2-hydroxyphenazine. Assuming a two-electron MAPK inhibitor transfer from the MP analog, 212 μM free thiol groups would

be expected. These results indicate that MP is a component of the membrane-bound electron transport chain terminating with reduction of CoM-S-S-CoB. Figure 5 Reduction of 2-hydroxyphenazine and re-oxidation dependent on membranes and CoM-S-S-CoB. The 100-μl reaction mixture consisted of membranes (107 μg protein), 4 μM ferredoxin, 100 μM 2-hydroxyphenazine and CdhAE (40 μg) in 50 mM MOPS (pH 6.8) under 1 atm CO. The reduction and oxidation of 2-hydroxyphenazine ACP-196 research buy was followed by the absorbance at 475 nm (ε475 = 2.5 mM-1 cm-1). CdhAE was added to initiate the reduction at time zero. At point A the cuvette was flushed with 100%

N2 and 2 μl of MOPS buffer (pH 6.8) was added. At points B and C, 2 μl of MOPS buffer (pH 6.8) containing CoM-S-S-CoB was added to the reaction reaching final concentrations of 240 and 480 μM. The results implicating MP and cytochrome c in the membrane-bound electron transport chain presents the possibility of electron transfer between these carriers. The MP analog 2-hydroxyphenazine re-oxidized cytochrome c when added to membranes of acetate-grown cells previously reduced with ferredoxin (Figure 6). These results suggest that MP is Decitabine either directly or indirectly linked to cytochrome c, a result

further supporting the participation of MP and cytochrome c in the membrane-bound electron transport chain. Figure 6 Oxidation of membrane-bound cytochrome c by 2-hydroxyphenazine. The 100-μl reaction mixture consisted of membranes (750 μg protein), 4 μM ferredoxin 1 mM NADPH and1 μg FNR contained in 50 mM MOPS buffer (pH 6.8). The reduction of cytochrome c was initiated by addition of FNR. The reduction and re-oxidation was monitored at 554 nm. When fully reduced, 200 μM 2-hydroxyphenazine (2 μl) was added (arrow). Panel A, time course for the reduction and re-oxidation by 2-hydroxyphenazine added at the arrow. Panel B, reduced minus oxidized UV-visible spectra of membranes before (lower trace) and after (upper trace) addition of 2-hydroxyphenazine. Discussion The overwhelming majority of methanogens capable of growth via conversion of the methyl group of acetate to methane do not metabolize H2 suggesting they employ an electron transport pathway distinct from that proposed for the few acetotrophic methanogens in which H2 is an obligatory intermediate. M.