L‐aspartic acid and urea supplementation of low‐protein layer diets1

1. Urea supplementation of low‐protein (125 g/kg) conventional‐type diets for layers, whether containing fish meal or not, did not appear advantageous.

2. Supplementation of the low‐protein diet with aspartic acid did not affect egg production rate or efficiency.

3. Soyabean meal supplementation of the low‐protein diet increased egg weight significantly whereas aspartic acid did not.     

Response of broiler chickens to well‐balanced protein mixtures

1. Four experiments were conducted on broiler chickens between one and three weeks of age to determine their response to dietary protein concentrations.

2. Diets prepared by serial dilution of a concentrated protein mixture, well‐balanced with respect to all essential amino acids, were fed in three experiments, while in a fourth experiment, a lysine‐deficient protein mixture was used.

3. Response curves relating body‐weight gain to increasing concentrations of protein and of lysine intake are presented.

4. A table is presented from which optimum protein intakes can be calculated according to changes in input and output costs and changes in growth potential of the chickens.     

Genotype‐level of protein interaction for growth rate in broilers

1. Two groups of White Plymouth Rock which were related to each other as half‐sibs were fed on diets containing either a normal or reduced amount of protein.

2. Compared with the normal diet the low‐protein diet caused a decrease in growth rate which at 38 d was 37% and 25% for male and female chickens, respectively.

3. A genotype‐level of protein interaction was demonstrated for weight at 38 d. Expressed as a genetic correlation for the same trait and measured in the two feeding environments the values were about 0.33.

4. In estimating the genetic correlation the interaction as well as the covariance method were used. The two methods did not give the same estimates.

5. Heritabilities for weight at 38 d tend to be larger in the low‐protein environment.     

Differential effect of age on metabolisable energy content of high protein‐low energy and low protein‐high energy diets in young broiler chicks1

1. An experiment was carried out with 6‐d old male broiler chicks in an attempt to understand better the effect of age on dietary AME_n of high protein‐low energy (HPLE) and low protein‐high energy (LPHE) diets which are used in the determination of the AME_n content of grains when substituted for the entire diet. The experiment was carried out in a split‐plot design in which the effects of 2 diets (HPLE‐reference and LPHE‐test, containing maize) on food intake, faecal excretion, dietary AME_n and the utilisation of the nutrients were evaluated in 3 age periods (A = 11–13, B = 15–17 and C = 20–22 d of age).

2. Chicks fed on the HPLE diet consumed significantly less food than those fed on the LPHE diet during periods A and B, but not in G. They also produced a significantly larger amount of droppings during periods B and C. Food‐to‐droppings ratio, which was consistently and significantly lower in chicks fed on the HPLE diet, decreased markedly in period C only in these birds.

3. Absolute and relative retention (RR) of dry matter (DM) and starch, and RR of nitrogen (N) from birds fed on the HPLE diet, were consistently and significandy lower than from those fed on the LPHE diet, but fat retention (absolute and relative) was higher. RR of DM and of N in period C was significantly lower than in periods A and B, while RR of fat and of starch was not affected by age. The effect of age on RR of N was observed only with the HPLE diet.

4. AME_n of the HPLE diet, but not of the LPHE diet, in period C was significandy lower than in periods A and B, resulting in a significant interaction between age and diet and a general reduction with age. The calculated AME_n contents of the maize in periods A and B were essentially the same (14.91 and 14.85 MJ/kg, respectively), and lower than in period C (15.28 MJ/kg). It is concluded, therefore, that because of its effect on AME_n of the HPLE reference diet in chicks older than 17 d, bird age is of considerable importance in the determination of AME_n in grains when substituted for the entire diet.     

Maximum nutritional response to poor‐quality protein and amino acid utilisation

1. Although the theory of responses to amino acids suggests that, providing sufficient of the limiting amino acid is fed, it should be possible to elicit maximum growth response, maximum response is not usually elicited by poor‐quality proteins.

2. It has been suggested that this failure to elicit maximum response is a reflection of poorer limiting amino acid utilisation from poor‐quality proteins. This interpretation conflicts with the theory of general amino acid imbalance which proposes that amino acid excesses do not impair the utilisation of the limiting amino acid.

3. Three protein mixtures of different quality were made by mixing maize gluten meal and soyabean protein concentrate in constant proportions, supplementing with tryptophan, threonine and arginine to adequacy and varying amino acid score (0'62, 0^‐71 or = 1–0) by varying additions of free lysine. The 3 mixtures were diluted with protein‐free ingredients to produce 3 diet series, each providing 3–7, 6–5, 9–2, 120, 14–8 and 17–5 g lysine per kg. Each diet was fed to 4 cages of 2 chickens each from 4 to 14 d of age in a randomised block experiment. Food intake, body‐weight and body‐nitrogen gain were measured.

4. Differences in protein quality were confirmed by regression analyses of body‐weight response to protein intake (Net Protein Ratio) and body‐nitrogen response to nitrogen intake (Net Protein Utilisation) in the linear range. Regression analyses in the linear range of body‐weight or body‐nitrogen response to lysine intake showed no adverse effect of protein quality on lysine utilisation. Curvilnear analysis (Reading flock response model) confirmed this finding.

5. Maximum response could not be obtained with the poorest protein quality. It is illogical to invoke impaired utilisation of the limiting amino acid to explain this. A small decrease in net energy yield of the diet may be sufficient to explain the effect, but it is more likely that the depletion of the limiting amino acid from tissue (muscle) protein which results from feeding poor‐quality protein explains the effect.     

Urea and aspartic acid supplementation of low‐protein broiler diets1

1. L‐Aspartic acid does not seem useful as a protein surrogate in conventionally formulated low‐protein diets for broiler chicks.

2. Urea as a protein substitute does not enhance the value of conventional broiler diets.

3. Urea does not improve broiler diets that have been supplemented with fish meal or crystalline amino acids to satisfy requirements for all indispensable amino acids.

4. Urea is absorbed into the bloodstream, but is not assimilated into body proteins.     

Short‐term effects of food protein content on subsequent diet selection by chickens and the consequences of alternate feeding of high‐ and low‐protein foods

1. Growing male chickens of broiler and layer strains were allowed to eat either a high‐protein food (HP) or a low‐protein food (LP) for 10 min after an overnight fast and then offered a choice between HP and LP. During the next hour they ate significandy more of the food other than die initial meal. Similar results were obtained when there was a gap of 45 min without food between the initial meal and the choice period.

2. When the initial meal was given by tube into the crop, followed by 45 min without food, there was no significant effect on subsequent diet selection. These results show that it is necessary for the birds to eat the food themselves for it to exert its effect on subsequent choice.

3. Birds with experience of eating two foods identical in nutrient composition but different in colour did not select either food in preference to the other following an initial meal of one alone. This is evidence against the possibility that neophagia accounts for the results of the first two experiments. When an initial meal of low protein food was followed by a choice of high and low protein foods, birds ate a greater proportion of the high protein when it was placed on the opposite side of the cage from that in which the initial meal was given. Thus they are not choosing a food simply by its position within the cage.

4. To see the extent to which broilers can extend their ability to compensate for protein content over several weeks, male broilers were given one of 4 treatments from 5 to 10 weeks of age: (A) HP and LP concurrendy; (B) HP and LP on alternate days; (C) HP in the morning and LP in the afternoon, (D) LP in the morning and HP in the afternoon. There was no significant effect of treatment on food intake, body weight gain or carcase protein content but carcases were significantly less fat after treatment (B) than treatment (D).

5. It is concluded that growing broiler chicks can compensate well for periods of access to only a low‐protein food, by subsequent intake of a high‐protein food, and lice versa, as long as they are able to gauge the sensory properties of the foods. Offering two complementary foods in alternating half‐day periods is an effective method of choice‐feeding, allowing birds to select a diet to meet the requirements for growth.     

Comparison of a 19.7%‐protein wheat (triticum aestivum L), three 13.5%‐protein wheats,and corn (zea mays) in broiler diets with different protein and lysine contents

An experiment using broiler chicks up to 3 weeks of age was conducted to examine the use of corn (Zea mays), Glenlea, Pitic 62, 13.5%‐protein Neepawa and 19.7%‐protein Neepawa wheats (Triticum aestivum L) as ingredients in broiler diets. Two dietary protein contents (calculated as 18.5 and 23.0%) with and without supplementary lysine (0.3%) were used in the diets containing each of the five grains. The desired dietary protein contents were obtained by varying the proportions of the grains and soybean meal.

Grain, dietary protein and added dietary lysine significantly affected body weights and efficiencies of food conversion.

Significant first‐order interactions between grain x protein, grain x lysine and protein x lysine were found for both body weights and efficiencies of food conversion and resulted mainly from responses obtained with the 19.7%‐protein Neepawa wheat supplemented with lysine when compared with the responses obtained to the other grains. When substituted into the higher‐protein diet, supplemented with lysine, the 19.7%‐protein Neepawa wheat supported a similar performance in chicks to other grains fed under similar conditions.     

The use of n‐paraffin‐grown yeast as the main source of protein in diets for chicks

1. n‐Paraffin‐grown yeast and a mixture of soyabean meal and fish meal were compared in the net protein utilisation (NPU) test, and as protein supplements in diets for broilers up to 4 weeks of age.

2. The difference between the NPU values, 0.66 for yeast and 0.80 for the soyabean meal and fish meal mixture, could largely be attributed to the high nucleic acid content of the yeast.

3. Chicks given the diet containing yeast (190 g/kg) did not grow as rapidly as those given the soyabean meal and fish meal reference diet, and the reduced growth could only partly be explained by a marginal deficiency of methionine.

4. Food conversion efficiency with the yeast diet was improved by maize oil while responses to α‐tocopheryl acetate and sodium selenite were inconsistent.

5. Chicks grew well when yeast replaced fish meal in the mixture of soyabean meal and fish meal, and when fish meal (194 g/kg diet) was the sole protein supplement.     

The diagnostic value of plasma proteins and non‐protein nitrogen substances in birds

Summary

This paper summarises current knowledge of the diagnostic value of avian plasma proteins and non‐protein nitrogen substances.

Reference values for total protein, the albumin: globulin ratio, uric acid, creatinine, and urea for various avian species are presented. The importance of the albumin:globulin ratio and the urea:uric acid ratio is emphasised.     

Evaluation of methanol‐grown bacteria and hydrocarbon‐grown yeast as sources of protein for poultry: Studies with young chicks

1. In a series of five trials, conducted with broiler chicks during the starting period, two types of dietary single‐cell protein were tested: Pruteen (PR), a protein concentrate produced from methanol‐utilising bacteria, and a Lavera‐type yeast (LA) utilising the normal paraffins of heavy gas oil.

2. The inclusion of 90 to 150 g PR or LA/kg diet depressed growth rate by 14 to 16% and 9 to 10%, respectively. This effect was slightly counteracted (about 6 percentage units) by the addition of L‐arginine.

3. The growth depression can be explained completely in the case of PR or almost completely in that of LA on the basis of reduced food intake, without a decided effect on food utilisation.

4. The reduced consumption of PR‐containing diets is not due to a petroleum‐ether‐soluble factor, nor to the high and low concentrations of sodium and potassium, respectively, in PR.     

The effect of feeding low‐protein diets to pullets from hatch to point‐of‐lay and the quantitative restriction of food during the subsequent laying period

Pullets from two commercial breeds were fed on diets of similar energy content but with 19% or 16% crude protein to 8 weeks of age and from 8 to 20 weeks of age on one of three isoenergetic diets containing either 12, 14 or 16% crude protein. At 20 weeks the birds were offered a conventional layers’ diet containing 16% crude protein either ad libitum or on a daily food intake of 100 g for a further 32 weeks.

The results indicate that with certain breeds the dietary protein levels can be lowered to approximately 16% during the o to 8‐week period and to approximately 12% during the 8 to 20‐week period without adversely affecting egg production. However, variations in the laying performance of the different breeds appear to be dependent on the amount of protein fed in the first eight weeks of life. Significant breed effects were observed throughout the experiment and although restricted feeding during the laying period substantially reduced the food intake it also had a detrimental effect on the rate of egg production and on the total weight of eggs produced.     

Effects of oven‐drying tubers of two high‐protein sweet potato varieties at different temperatures on their feeding value in broilers

1. Unpeeled tubers from 2 high‐protein varieties of sweet potato (white‐fleshed Bosbok, and orange‐fleshed Carmel) were chipped and oven‐dried at 40, 60, or 80°C, to examine the effects on nutritive value. The dried ground chips were substituted for maize at 500 g/kg and the diets fed to day‐old, Ross‐1 broiler chicks for 3 weeks.

2. Compared with Carmel, Bosbok had a lower crude protein content (90 v. 138 g/kg DM) and trypsin inhibitor activity (TIA) (3 v. 5 mg of trypsin inhibited per g flour). Processing did not significantly affect TIA, but the lysine and cystine contents were lowered and the starch content raised as the drying temperature increased. However, whereas this was reflected in increased reducing sugars in Carmel, there was no trend in Bosbok.

3. The results of in vitro pancreatin digestibility and total dietary fibre assays showed variety and processing temperature to be significant factors influencing the nutritive value of sweet potato tubers, with a variety X temperature interaction also being indicated. The interaction was also observed for weight gain, dry matter intake, water: food intake ratios, excreta water content, presence of bile in excreta and liver weights. The best growth was obtained with Bosbok dried at 60°C, for which liveweights at 21 d were 11% lower than for the maize controls.     

Influence of protein concentration on the sulphur‐containing amino acid requirement of broiler chickens 1

1. Two experiments were conducted with male broiler chickens from 3 to 6 weeks of age to determine the effect of dietary protein content on the requirement for sulphur amino acids (SAA). In experiment 1, 0, 0.5, 1.0 or 1.5 g DL‐methionine/kg were added to diets calculated to contain 200, 240 or 280 g protein/kg. In experiment 2, 0, 0.6, 1.2 or 1.8 g DL‐methionine/kg were added to diets calculated to contain 160, 180 or 200 g protein/kg.

2. In experiment 1, the SAA requirement for body weight gain increased as dietary protein content increased. Regression analysis indicated a requirement of 38 g SAA/kg protein.

3. In experiment 2 in which lysine supplementation provided a minimum of 10 g/kg, the requirement for SAA per unit of diet increased only slightly as protein concentration increased indicating that below 200 g protein/kg of diet, the SAA requirement increases per unit of protein with supplementation of the second‐limiting amino acid.

4. Abdominal fat percentage declined in a linear manner with each increment of SAA added to diets containing 160 to 200 g protein/kg. Adding methionine to diets containing 240 or 280 g protein/kg did not affect abdominal fat content. A lower limit of abdominal fat was achieved with a protein concentration of 240 g/kg.

5. It is concluded that the requirement for SAA of finishing broiler chickens is directly related to protein content at concentrations of 200 or more g protein/kg but increases per unit of protein at lower protein concentrations when a minimum lysine concentration is specified. Abdominal fat content reaches a minimum between 200 and 240 g protein/kg of a maize‐soyabean meal diet regardless of SAA content.     

Time course of oxidative phosphorylation in liver mitochondria of chickens fed on high‐protein diet

1. Progressive alterations in oxidative phosphorylation of liver mitochondria were followed for 14 d in growing chickens fed on either semi‐purified low (7%) or high (61%) protein‐energy diet. Hepatic mitochondrial oxidative phosphorylation rates were assessed polarographically with pyruvate + malate as substrates.

2. The ADP:O values were reduced significantly 4 d after the feeding of a high‐protein‐energy diet, when compared with those in chickens fed on a low‐protein‐energy diet, whereas the state 3 oxidation rates in chickens fed on a high‐protein‐energy diet from day 6 to 14 were significantly lower than those in low‐protein‐fed chickens.

3. No changes in sensitivity of mitochondrial ATPase activity to oligomycin, expressed as % of total ATPase activity, were observed among chickens fed for 21 d on diets with various protein concentrations though the FoF₁‐ATPase activity, expressed per mg protein, tended to decrease in chickens fed on high‐protein‐energy diet.

4. These results suggest that the reduced ADP:O values for liver mitochondria in the high‐protein‐fed chickens may not be involved in the degrees of integrity of the FoF₁‐ATPase.     

Evaluation of methanol‐grown bacteria as a source of protein and energy for young chicks

1. The inclusion of 100 or 200 g/kg spray‐dried methanol‐grown bacteria in unpelleted semi‐purified diets reduced growth rate and efficiency of food conversion of young chicks over a 14 d period.

2. Classical metabolisable energy values for the spray‐dried product, at relatively low inclusion rates, ranged from 9.55 to 10.92 MJ/kg dry‐matter (DM) and nitrogen‐corrected values ranged from 8.95 to 10.16 MJ/kg DM.

3. Inclusion of 96 g/kg flash‐dried methanol‐grown bacteria in unpelleted semi‐purified diets marginally increased growth rates, efficiency of food conversion and nitrogen utilisation of chicks, but higher inclusions of up to 290 g/kg caused adverse effects.     

The nitrogen‐sparing effect of methionine in chicks receiving a protein‐free diet supplemented with arginine: Effect of various methionine substituents

1. The nitrogen‐sparing effect of methionine in chicks fed on a protein‐free diet containing arginine was examined in three 10‐d trials. Chicks received either a protein‐free diet, this diet supplemented with arginine and methionine or diets containing arginine in which the methionine was replaced by various methionine‐related compounds.

2. Body‐weight changes, nitrogen retentions and uric acid‐nitrogen excretion indicated that the methyl moiety was unlikely to contribute to nitrogen sparing activity and that cysteine, or possibly glutathione, played an important role. The possible mechanism of the nitrogen‐sparing effect is discussed.     

Relationship between energy and protein intakes and laying characteristics in individually‐caged broiler breeder hens

1. Individually‐caged broiler hens, which had been reared on an advised rationing programme, were fed allowances of 1.88, 1.61, 1.32 or 1.13 MJ apparent metabolisable energy/bird d at four different protein intakes (27, 23, 19.5 or 16.5 g crude protein per bird d) from 21 to 60 weeks of age.

2. Age at first egg, body‐weight gain and egg production were affected by energy allowance. Birds on the lower energy allowances came into lay later than birds on the higher energy allowances and at a lower body weight.

3. Body‐weight gain decreased with decreasing energy allowance. The decrease in egg output in response to decreasing energy allowance resulted from more birds ceasing to lay and fewer birds laying on more than 3 d per week. Similar changes in the distribution of rates of lay were observed on each treatment as the flock aged.

4. The relationship between body‐weight gain and egg number on each treatment was negative from 21 to 36 weeks, but became less consistent with age.

5. Protein intake had little effect on body weight. At the lowest energy allowance, egg number and egg weight decreased with increasing protein allowance. This effect was not observed on the higher energy allowances.     

Evaluation of methanol‐grown bacteria and hydrocarbon‐grown yeast as sources of protein for poultry: Performance of broilers during the finishing period

1. Three trials were carried out with male broilers during the 5‐ to 8‐week period, for the evaluation of two types of single‐cell protein (SCP) in practical‐type broiler finisher diets. The SCP tested were: Pruteen, produced from methanol‐utilising bacteria, and a Lavera‐type yeast which utilises the normal paraffins of heavy gas oil.

2. The inclusion of 90 to 100 g of either type of SCP/kg of the diet caused a 2 to 3% reduction in weight gain, a 3 to 5% decrease in food consumption, and up to a 2% improvement in food utilisation. The reduced growth rate could be fully explained by the decrease in food intake, with essentially no effect on food : gain ratio.

3 In diets containing Pruteen, arginine was second limiting after the sulphur amino acids.

4 An odd‐numbered fatty acid (17 carbons, unsaturation unknown) of Pruteen was not found in the carcass lipids of broilers fed on a diet containing 120 g Pruteen/kg.