A. Gehin et al., STUDIES OF CLOSTRIDIUM-CELLULOLYTICUM ATCC-35319 UNDER DIALYSIS AND COCULTURE CONDITIONS, Letters in applied microbiology, 23(4), 1996, pp. 208-212
The degradation of cellulose by Clostridium cellulolyticum has been st
udied in several ways: (1) in batch fermentation in 50-ml sealed-cap f
lasks, referred to as the control; (2) in batch fermentation with pH a
t 7.2; (3) fermentation in dialysis which permits elimination of all t
he products of metabolism; (4) fermentation in dialysis with a constan
t bubbling of nitrogen; (5) in co-culture with Clostridium A22 in batc
h. with and without pH regulation and with dialysis. H-2, CO2, acetate
, ethanol and lactate were the major end-products of cellobiose and ce
llulose fermentation. Compared to batch culture, growth of Cl. cellulo
lyticum on cellobiose increased by a factor of 10 in dialysed culture.
The end products from the dialysed culture were detected in a small r
ange compared to the concentration for the batch culture. Related to t
he biomass, CMCase activities were of the same level, showing a direct
relation between the biomass formation and the cellulase production.
The percentage of cellulose degradation (50%) by Cl. cellulolyticum wa
s greater when dialysis of end products with a constant bubbling of ni
trogen tool; place during the course of fermentation (6 d) in comparis
on with cultures in 50-ml sealed-cap flasks (23%), in a fermenter (36%
) or using dialysis without N-2 bubbling (40%). The presence of two mi
cro-organisms produced no further enzyme activities and hence the perc
entage of cellulose degradation was quite similar in mono- and co-cult
ure. No synergistic action was found between two cellulolytic strains.