Published online by Cambridge University Press: 09 March 2007
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 phosphate-citrate 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 wasdue 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 thediet 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 digestibilitieswere 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 asmall amount of non-reactive 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