Two commercial preparations of polysaccharide-degrading enzymes (El and E2)
were tested in vitro and in vivo for rumen stability. In vitro the enzymes
were incubated with rumen fluid and the recovery of the remaining substrat
e-degrading activities (CMC-ase, xylanase and amylase) were followed for up
to 6 h (Exp. 1). In vivo the enzyme preparations were introduced directly
into the rumen of a lactating dairy cow fed a mixed forage/concentrate diet
(Exp. 2). Rumen and duodenal samples were analyzed for substrate-degrading
activities (CMC-ase, xylanase, beta-glucanase and amylase) for up to 15 h
after the enzyme was administered. The tested enzyme preparations were rema
rkably resistant to microbial fermentation in in vitro conditions. Compared
to the control, addition of exogenous enzymes to the rumen increased (P<0.
05) the average polysaccharide-degrading activities of the lumen fluid by 1
69%, 49%, and 61% and 198%, 375%, and 107% for CMC-ase, xylanase and beta-g
lucanase activities, El and E2, respectively. The xylanase component of one
of the enzymes (E2) partially escaped the reticulo-rumen and the abomasum
and increased the xylanase activity of duodenal digesta to 23.3 compared to
0.84 nmol ml(-1) min(-1) for the control (P<0.05). These data suggest that
some exogenous enzymes may by-pass the forestomach and may eventually affe
ct the utilization of nutrients in the small intestine of ruminants. (C) 19
98 Elsevier Science B.V.