Experiments were made to estimate separately the amino acid requirements of growing pigs for maintenance and for protein accretion. The relationship between nitrogen retention and amino acid intake was estimated for each essential amino acid (except histidine) by giving, at rates of N intake of 0.25 and 2.0 g/kg body-weight (W)0'75 per d, diets in which one amino acid was made specifically deficient. From the regression coefficients it was calculated that, for the accretion of 1 g body protein, the dietary amino acid requirements were (mg) threonine 47, valine 53, methionine + cystine 36, methionine 19, isoleucine 43, leucine 78, phenylalanine + tyrosine 84, phenylalanine 41, lysine 68 and tryptophan 12. The daily amino acid requirements for N equilibrium were also estimated. From the relationship between N retention and amino acid intake the daily amino acid requirements for N equilibrium were estimated to be (mg/kg Wo75 per d) threonine 53, valine 20, methionine+ cystine 49, methionine 9, isoleucine 16, leucine 23, phenylalanine + tyrosine 37, phenylalanine 18, Iysine 36 and tryptophan 11. It was estimated that both for maintenance and for protein accretion tyrosine could provide close to half the total phenylalanine + tyrosine needs. Cystine could supply close to half the total sulphur amino acid needs for protein accretion but 0 8 of the needs for maintenance.

Intact male pigs from two nucleus breeding herds (one predominantly Duroc, DM; the other purebred Large Wliite, LM) together with intact male (RM), castrated male (RC) and female (RF) commercial hybrid pigs were given one of two diets, with the same balanced protein (180 or 240 g/kg) at three daily rates, the highest being 'to appetite'. Six replicates of 30 pigs were allocated to these regimes at 40 kg: one replicate was slaughtered immediately to determine initial carcass composition; the remaining pigs were slaughtered at 85 kg when carcass fat and specific gravity (SG) were measured. For two replicates this was followed by dissection and chemical analysis: daily gains of carcass lipid and protein were estimated directly for these two replicates and predicted from carcass weight and SG for the other three. Fed 'to appetite', castrated males and females ate more than males; LM pigs ate least. All males grew faster than females or castrated males, the DM pigs the fastest, these rankings being relatively insensitive to feeding level. However, both in daily weight gain and daily protein accretion only the males responded to additional dietary protein. Daily body protein accretion of DM pigs increased linearly with intake on both diets whereas LM pigs showed little response to the highest level of feeding. At the same daily protein intake all pigs had higher rates of body protein accretion on the low protein diet, showing that they were sensitive to additional dietary energy. Results indicate that an animal's superiority may result from a greater efficiency of protein utilization or a higher lean growth potential but that these two characteristics are not simply related.

No abstract

No abstract

The optimal balance of amino acids in the diet of the growing pig was estimated by ARC (1981) on the basis of a number of disparate studies augmented by data on the amino acid composition of the whole body on the premise that the amino acids incorporated into accreted body proteins are the major determinant of requirements and that this pattern is not distorted by inequalities in the utilisation of individual amino acids. In an accompanying paper (Wang & Fuller, paper no. 91) an optimal pattern was derived by direct experiment which was shown to be utilised better than that described by ARC (1981). That pattern, however, which related to one particular rate of nitrogen input and the particular rate of protein accretion which that input supported, includes two components, a requirement for maintenance and a requirement for protein accretion. There is clear evidence from studies with rats and chicks that the optimal pattern of amino acids for maintenance and growth are quite different and so the optimal pattern for any particular rate of growth will depend on the relative contributions of the two components. The purpose of this experiment was to estimate both.