The apparent ileal digestibility coefficients of amino acids in 107 samples representing 22 food ingredients were determined using 6-week-old broiler chickens. The ingredients assayed included five cereals (barley, maize, sorghum, triticale and wheat), two cereal by-products (rice polishings and wheat middlings), four oilseed meals (canola, cottonseed, soya-bean and sunflower meals), full-fat canola, maize gluten meal, four grain legumes (chickpeas, faba beans, field peas and lupins) and five animal protein sources (blood, feather, fish, meat and meat and bone meals). The mean ileal digestibility coefficients of amino acids in wheat and maize were higher than those in sorghum, triticale and barley. However, variations observed in individual amino acid digestibilities among samples within cereal type were greater than those determined between cereals. Threonine and lysine were the least digestible indispensable amino acids in the five cereals evaluated. The most digestible indispensable amino acid was phenylalanine in wheat and, leucine in maize and sorghum. In the case of the wheat middlings and rice polishings, threonine was the least digestible indispensable amino acid and arginine was the best digested.In the oilseed meals assayed, amino acid digestibility was highest for soya-bean and sunflower meals, intermediate for canola meal and lowest for cottonseed meal. Ileal digestibility coefficients of amino acids in lupins were found to be slightly lower than those in soya-bean meal. The amino acid digestibilities of field peas, faba beans and chickpeas were considerably lower than those of lupins. Digestibility of arginine was the highest and that of threonine was the lowest of the indispensable amino acids in oilseed meals and grain legumes, except in cottonseed meal. Lysine was the least digestible amino acid in cottonseed meal.In the animal protein sources assayed, digestibility coefficients of amino acids in blood meal were high, intermediate in fish meal, and low in meat meal, meat and bone meal and feather meal. Variation in amino acid digestibility coefficients determined for blood meal samples was small. However, wide variations in amino acid digestibilities were observed for other animal protein sources, highlighting significant batch-to-batch differences. In particular, marked variations were determined for meat meal and meat and bone meal samples. Cystine was the least digested amino acid in animal protein meals, with the exception of blood meal in which isoleucine had the lowest digestibility. The limitations of using apparent digestibility values in diet formulations and the concept of the standardized digestibility system to overcome these limitations are discussed.
The influence of microbial phytase on the ileal amino acid digestibilities in three cereals (corn, sorghum, and wheat), four oilseed meals (soybean meal, canola meal, cottonseed meal, and sunflower meal) and two cereal by-products (wheat middlings and rice polishings) was determined using 5-wk-old broilers. Supplementation of microbial phytase (1,200 FTU/kg) improved (P < 0.001 to 0.10) the digestibilities of protein and amino acids in all feedstuffs, but the magnitude of response varied depending on the feedstuff and the amino acid considered. Mean digestibility of the 15 amino acids in the feedstuffs without and with phytase were: corn, 78.0 and 80.4%; sorghum, 74.7 and 79.4%; wheat, 77.7 and 84.6%; soybean meal, 82.2 and 85.5%; canola meal, 78.7 and 80.7%; cottonseed meal, 70.8 and 74.2%; sunflower meal, 76.7 and 80.2%; wheat middlings, 70.8 and 73.4%; and rice polishings 62.1 and 66.9%, respectively. When individual amino acids were considered, the increments in digestibility were relatively higher for threonine and valine. This effect was consistent across all feedstuffs. The observed variations in response among feedstuffs were influenced by the inherent protein digestibility, but not by dietary phytic acid concentration. No correlations were determined between the dietary concentrations of phytic acid and phytase responses in terms of protein digestibility (r = 0.20; P > 0.31) and mean amino acid digestibility (r = 0.12; P > 0.51); however a significant negative correlation was observed between inherent protein digestibility and phytase responses in protein digestibility (r = -0.42; P < 0.03). It appears that solubilities of phytate salts and protein, and their influence on the degree of phytate-protein complexing in different feedstuffs, may be more relevant than total phytic acid concentrations. Interestingly, dietary phytic acid concentrations were negatively correlated with inherent protein (r = -0.81; P < 0.001) and mean amino acid (r = -0.85; P < 0.001) digestibilities of the feedstuffs evaluated in this study.
1. Male broilers (n=900) were fed on wheat-sorghum-soyabean meal based diets containing 3 concentrations of phytic acid (10.4, 13.2 and 15.7 g/kg; equivalent to 2.9, 3.7 and 4.4 g/kg phytate P), 2 concentrations of non-phytate (or available) phosphorus (2.3 and 4.5 g/kg) and 3 concentrations of microbial phytase (0, 400 and 800 FTU/kg) from day 7 to 25 post-hatch. The dietary concentrations of phytic acid were manipulated by the inclusion of rice pollards. All diets contained celite (20 g/kg) as a source of acid-insoluble ash. 2. The apparent metabolisable energy (AME) concentrations of the diets were determined using a classical total collection procedure during the 3rd week of the trial. On d 25, digesta from the terminal ileum were collected and analysed for phosphorus, nitrogen and amino acids. Nutrient digestibilities were calculated using acid-insoluble ash as the indigestible marker. 2. Ileal digestibilities of nitrogen and essential amino acids were negatively influenced by increasing dietary levels of phytic acid but these negative effects were overcome by the addition of phytase. 3. Supplemental phytase increased AME, ileal digestibilities of phosphorus, nitrogen and amino acids and the retention of dry matter, phosphorus and nitrogen in broilers. There were no differences in the phytase responses between additions of 400 and 800 FTU/kg. 4. The responses in all variables, except AME, were greater in low non-phytate phosphorus diets. 5. In the case of AME, the response to added phytase was greater in adequate non-phytate phosphorus diets. Supplemental phytase increased AME values from 13.36 to 13.54 MJ/kg dry matter in low non-phytate phosphorus diets and from 12.66 to 13.38 MJ/kg dry matter in adequate non-phytate phosphorus diets.
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