Iv. Pibernat et Ca. Abella, SULFIDE PULSING AS THE CONTROLLING FACTOR OF SPINAE PRODUCTION IN CHLOROBIUM-LIMICOLA STRAIN UDG-6038, Archives of microbiology, 165(4), 1996, pp. 272-278
Chlorobium limicola UdG 6038, a green sulfur bacterium, was isolated f
rom anoxic sediments. Cells were gram-negative, non-motile, ovoid shap
ed, and contained chlorobactene and bacteriochlorophyll c as the main
photosynthetic pi,aments. The DNA G+C content was 56.4 mol%. Ultrastru
ctural studies revealed the presence of abundant spinae (45-110 spinae
per cell) attached to the cell wall. India-ink-stained cells observed
under the optical microscope were surrounded by a large capsule (5-11
mu m total diameter). The presence of this capsule was coincident wit
h the presence of a large number of spinae (> 30 spinae per cell). The
mucilaginous capsule was attached to the spinae without penetrating i
t. In batch culture, the synthesis of spinae in strain UdG 6038 was no
t affected by changes in temperature, pH, salt concentration, or illum
ination at physiological ranges and hence, the cells remained spined.
The control of spinae production was experimentally confirmed using a
semicontinuous batch culture refed by sulfide pulsing. The culture rem
ained at a low spination level (< 30 spinae per cell) only when the du
ration of sulfide starvation between pulses was less than 5 h. After l
onger sulfide starvation periods, the cells remained spined (more than
38 +/- 6.3 spinae per cell). This observation supports the idea that
the duration of sulfide limitation in the culture plays a key role in
controlling the spination process in strain C. limicola UdG 6038. Chlo
robium spinae may play an eco-physiological role in buoyancy capacity
and adhesion of sulfur globules to the cells in natural environments w
here sulfide concentrations are expected to be highly variable.