The pathway of sulfide oxidation with oxygen as electron acceptor was
studied with five strains of freshwater, marine and alkaliphilic sulfa
te-reducing bacteria. Electrode measurements with washed cells indicat
ed that all strains oxidized sulfide to elemental sulfur. In a second
step, the elemental sulfur formed was disproportionated to sulfate and
sulfide. During this phase, most of the disappeared sulfide was forme
d back. Since oxygen could be replaced by nitrate or nitrite as electr
on acceptor, the described biphasic reaction was independent of molecu
lar oxygen. With Desulfobulbus propionicus and the alkaliphilic strain
Z-7935, sulfide back-formation started after oxygen was consumed comp
letely. By contrast, with the freshwater strains Desulfovibrio desulfu
ricans CSN (DSM 9104) and Essex 6 (DSM 2032) and the marine strain P1B
, sulfide back-formation already started before oxygen was consumed. T
he addition of hydrogen as electron donor increased simultaneously the
rate of aerobic respiration and sulfide back-formation. Both reaction
s stopped when the oxygen was consumed, indicating that the electron t
ransport to oxygen and sulfur was coupled. Sulfide-oxidizing activity
(84 nmol O-2 min(-1) (mg protein)(-1)) was found in the periplasmic fr
action prepared by osmotic shock treatment of suspensions of D. desulf
uricans CSN. This fraction oxidized sulfide with oxygen to elemental s
ulfur. It is concluded that in different sulfate-reducing bacteria sul
fide oxidation proceeds via a common pathway with the formation of ele
mental sulfur as intermediate and its disproportionation to sulfate an
d sulfide. The process is independent of molecular oxygen.