Ky. Ng et al., Production of hydrogen sulfide from tetrathionate by the iron-oxidizing bacterium Thiobacillus ferrooxidans NASF-1, J BIOSCI BI, 90(2), 2000, pp. 193-198
When incubated under anaerobic conditions, five strains of Thiobacillus fer
rooxidans tested produced hydrogen sulfide (H2S) from elemental sulfur at p
H 1.5. However, among the strains, T. ferrooxidans NASF-1 and AP19-3 were a
ble to use both elemental sulfur and tetrathionate as electron accepters fo
r H2S production at pH 1.5. The mechanism of H2S production from tetrathion
ate was studied with intact cells of strain NASF-1. Strain NASF-1 was unabl
e to use dithionate, trithionate, or pentathionate as an electron acceptor.
After 12 h of incubation under anaerobic conditions at 30 degrees C, 1.3 m
u mol of tetrathionate in the reaction mixture was decomposed, and 0.78 mu
mol of H2S and 0.6 mu mol of trithionate were produced. Thiosulfate and sul
fite were not detected in the reaction mixture. From these results, we prop
ose that H2S is produced at pH 1.5 from tetrathionate by T. ferrooxidans NA
SF-1, via the following two-step reaction, in which AH(2) represents an unk
nown electron donor in NASF-1 cells. Namely, tetrathionate is decomposed by
tetrathionate-decomposing enzyme to give trithionate and elemental sulfur
(S4O62--->S3O62-+S-0, Po. 1), and the elemental sulfur thus produced is red
uced by sulfur reductase using electrons from AH(2) to give H2S (S-0 + AH(2
)-->H2S + A, Eq. 2). The optimum pH and temperature for H2S production from
tetrathionate under argon gas were 1.5 and 30 degrees C, respectively. Und
er argon gas, the H2S production from tetrathionate stopped after Id of inc
ubation, producing a total of 2.5 mu mol of H2S/5 mg protein. In contrast,
under H-2 conditions, H2S production continued for 6 d, producing a total o
f 10.0 mu mol of H2S/5 mg protein. These results suggest that electrons fro
m H-2 were used to reduce elemental sulfur produced as an intermediate to g
ive H LS. Potassium cyanide at 0.5 mM slightly inhibited H2S production fro
m tetrathionate, but increased that from elemental sulfur 3-fold. 2,4-Dinit
rophenol at 0.05 mM, carbonylcyanide-m-chlorophenyl- hydrazone at 0.01 mM,
mercury chloride at 0.05 mM, and sodium selenate at 1.0 mM almost completel
y inhibited H2S production from tetrathionate, but not from elemental sulfu
r.