Degradation of lucerne stem cell walls by five rumen bacterial species

The rumen bacterial strains Butyrivibrio fibrisolvens Hl7c, Fibrobacter succinogenes S8S, Lachnospira multiparus 4°, Ruminococcus albus 7 and R. flavefaciens FD-l were compared individually and as a five-species mixture with a rumen inoculum for their ability to degrade lucerne (Medicago sativa L.) stem cell wall polysaccharides. Two maturity stages oflucerne (bud and full flower) were utilized as substrates and incubation periods of 24 and 96 h were employed. Lucerne stem substrates and fermentation residues were analysed for cell wall content and composition. Degradation of total cell wall polysaccharides and all polysaccharide fractions was greater for immature than for mature lucerne stems. The 96-h incubation resulted in significantly more degradation of all cell wall polysaccharides than did the 24-h incubation. The R. albus culture was able to degrade all cell wall polysaccharide fractions as well or better than any other culture, including the rumen inoculum. Co-culture of R. albus with the four other ruminal species did not improve degradation of any wall polysaccharides compared with R. albus alone. Microscopic examination indicated that R. albus and the five-species mixture appeared to degrade lucerne tissues in thin sections to almost the same extent as did rumen fluid. Additional keywords: Medicago sativa, tissues, in vitro