Abstract :
The effects of raw sweet lupin (Lupinus angustifolius) meal and its fractions on the growth and N
utilization of rats were determined in two NPU and five N balance experiments. Sweet lupinseed
grown in Western Australia, obtained as meal, unsupplemented (LMU), or fully supplemented with
required amino acids (360 g/kg diet) (LMFS) was tested. In addition, six fractions were tested:
aqueous non-dialysed extract at pH 7.0 (LPAND), dialysed extracts soluble (LPAD) and insoluble at
pH 7.0 (LPADI), buffer-soluble extract at pH 7.0 (BUSOL), buffer-insoluble extract after dialysis at
pH 7.0 (BUDI) and the residue (LMR) containing most of the material from meal insoluble in water
and phosphahitrate buffer. All diets based on fractions contained the same amounts of energy and
protein and were supplemented with amino acids, vitamins and minerals to target requirements.
Body N and lipid contents of rats fed on LMU and LMFS were reduced significantly in comparison
with rats fed on positive lactalbumin (LACT) and non-protein diets (NPC) as negative controls. This
was due in part to the lower retention of the absorbed N. As a result, the NPU and the biological
value (BV) of sweet lupinseed proteins were less than expected. Urea-N outputs of the LMU- and
LMFS-fed rats were also elevated. In contrast, true N and DM digestibilities of rats fed on LMU and
LMFS were not significantly affected by the difference in the energy content of the diet. The
replacement of lactalbumin in the diet with LPAND (196 g/kg), LPAD (148 g/kg), LPADI
(124 g/kg), BUSOL (136 g/kg) or BUDI (119 g/kg) reduced dry body weight, N and lipid contents,
NPU and BV compared with those obtained from the LACT control, even though the N and DM
digestibilities were not significantly different. Inclusion of the residue fraction (170 g LMR/kg) had
no apparent effect on any of the variables studied. Since sweet lupinseed had a small amount of nonreactive
lectin and LMR had some undesirable side-effects in these rats, it appears that the low
nutritional value of LMFS for rats (NPU 0.62) despite the very high level of digestibility of its N,
results from disturbances in N metabolism, and particularly from the low retention value of the
absorbed N.
