The motility of the purple sulfur bacterium Marichromatium gracile was inve
stigated under different light regimes in a gradient capillary setup with o
pposing oxygen and sulfide gradients. The gradients were quantified with mi
crosensors, while the behavior of swimming cells was studied by video micro
scopy in combination with a computerized cell tracking system. M. gracile e
xhibited photokinesis, photophobic responses, and phobic responses toward o
xygen and sulfide. The observed migration patterns could be explained solel
y by the various phobic responses. In the dark, M. gracile formed an simila
r to 500-mum-thick band at the oxic-anoxic interface, with a sharp border t
oward the oxic zone always positioned at similar to 10 muM O-2. Flux calcul
ations yielded a molar conversion ratio S-tot/O-2 of 2.03:1 (S-tot = [H2S]
+ [HS-] + [S2-]) for the sulfide oxidation within the band, indicating that
in darkness the bacteria oxidized sulfide incompletely to sulfur stored in
intracellular sulfur globules. In the light, M. gracile spread into the an
oxic zone while still avoiding regions with > 10 muM O-2. The cells also pr
eferred low sulfide concentrations if the oxygen was replaced by nitrogen.
A light-dark transition experiment demonstrated a dynamic interaction betwe
en the chemical gradients and the cell's metabolism. In darkness and anoxia
, M. gracile lost its motility after ca. 1 h. In contrast, at oxygen concen
trations of > 100 muM with no sulfide present the cells remained viable and
motile for ca. 3 days both in light and darkness. Oxygen was respired also
in the light, but respiration rates were lower than in the dark. Observed
aggregation patterns are interpreted as effective protection strategies aga
inst high oxygen concentrations and might represent first stages of biofilm
formation.