Influence of energy concentration and source on the utilization of feed protein and NPN in lambs. 2. 15N balance and utilization of pure protein and NPN

In an experiment 12 lambs of the merino species were divided into 4 groups. The variants HE received 740 or 718 EFU cattle/kg DM and the variants NE 689 or 671 EFU cattle/kg DM. The different energy concentrations resulted from differentiated quotas of dried sugar beet chips and wheat starch supplements. Within the variants, sub-variants with (HESZ, NESZ) or without (HES, NES) sugar supplements were formed. Due to varied DM intake, the average energy intake in all groups was 42 EFU cattle/kg LW0.75. N balance experiments using 15N-labelled urea were carried out, and 15N accumulation of N excretion was projected to a steady state. The partial utilization of pure protein and NPN in the ration was ascertained with the help of a 3-pool compartment model of N utilization in ruminants. In the non-amino acid N pool HE utilized 84% of NPN and NE 77% for the synthesis of amino and nucleic acids. The efficiency of protein synthesis in the amino acid N-pool were in HESZ 64%, HES 70%, NESZ 70% and NES 73%, resp. The total utilization of NPN is the sum of the partial utilization in the two pools, whereas the total utilization of pure protein is calculated from the true digestibility and the efficiency of the utilization in the AA-N pool. The total utilization of NPN for the synthesis of protein for the protein pool amounted to 40/35/41/33% and that of pure protein to 54/51/49/50%. Energy intake being identical, energy concentration did not have an influence on the utilization of pure protein and NPN, whereas NPN utilization was better in rations containing sugar. The pure protein in the ration was by 19 ... 52% better utilized than NPN.     

The energy metabolism of swine at a feed level of "live weight equilibrium"

10 castrated pigs each of a live weight (LW) of 35 kg and 115 kg were fed over 28 and 40 days resp. in a way that a live weight equilibrium was achieved. The pigs were kept individually and at a low mobility on perforated floors of zinc-plated sheet iron at an air temperature of 19 degrees C. The weighing 35 kg received 668 kJ ME/kg LW 0.75 per day and one half of the animals weighing 115 kg 635 kJ ME/kg LW 0.75 in a diet consisting of barley and bran. The other half of the animals weighing 115 kg received 514 kJ ME/kg LW 0.75 per day in a ration consisting barley, bran and dried skim milk. The crude protein content of the rations was 12.6 and 17.1% resp. of the DM, the crude fibre content amounted to 8-10% of the DM. Energy excretion in faeces and urine was calorimetrically measured. Up to the end of the experiment LW and the weight of the empty body (without ingesta) remained unchanged. For the measuring of energy retention, 4-5 zero animals each were analysed before the experiments. The pigs weighing 35 kg showed a daily loss of 39 g fat in the course of the 40-day experiment. The calculation of the energy balance showed that an intake of 790 kJ ME/kg LW 0.75 was necessary. This maintenance requirement, rather high in comparison with values from literature, can be explained with the emission of body heat on sheet iron floors and a crude fibre content of 9% in the rations. The pigs of the two groups of 115 kg LW were at an energy equilibrium at both nutrition levels. The lower maintenance requirement of the group fed with dried skim milk cannot exclusively be explained by the higher energetic utilization of the milk protein in the ration. The reason should be the more advanced age of the animals of the milk group. Although they had nearly the same live weight, their empty bodies contained 41% fat, the pigs of the barley/bran group, however, only 34%, both before and after the experiment.     

The energy maintenance requirement of growing pigs of different sexes given normal and high protein diets. 1. Experiments in castrates

Energy retention was measured alternately at 12 barrows, fattening hybrids of line 150 (150 X (L X E], at maintenance level (4 periods) and growth feeding (5 periods) in the live weight range between 32 and 134 kg, 6 animals each received rations with 17 and 45% crude protein resp. during the complete experimental period. The nutrition level did not have a significant influence on the digestibility level of the feed. The experiments carried out at maintenance level showed that the maintenance requirement of metabolizable energy in the experiments with 17% crude protein in the ration was 941, in the experiments with 45% crude protein in the ration 913kJ ME/kg LW0.62 and on average 927 kJ ME/kg LW0.62. Including the experiments with growth feeding one can conclude from a regression analysis, largely in agreement with the measured values, that 955 kJ ME/kg LW0.62 is the energy maintenance requirement. These values of maintenance requirement are by 50% higher than those derived from previous measurings. In contrast to expectations, the increase of protein concentration in the ration did not result in a higher energy maintenance requirement. The utilization of metabolizable energy for retention amounted to 74% for rations with a normal protein content and to 65% for those with a high protein content. The multiply regressive evaluation showed a utilization of metabolizable energy for fat retention of 79% and for protein retention of 53%.     

Studies on the evaluation of feed protein for ruminants. 1. Passage of nitrogen fractions to the duodenum of dairy cows fed different protein and carbohydrate sources

The duodenal passages of non-ammonia nitrogen (NAN), amino acid N (AA-N) and microbial N (MN) were measured in seven duodenal fistulated dairy cows (6130 kg FCM/305 d) during lactation receiving 30 different rations similar to those used in dairy practice. The rations consisted of roughage (protein-rich silages, hay) and concentrate mixture (corn, barley, oat) in a ratio of 60:40 on a DM basis or roughage/concentrate mixture/fodder beets in the proportions 60:20:20 or 60:0:40 respectively. N supplements consisted of soya bean meal and peas meal (untreated or treated with formaldehyde in each case), rapeseed meal, fish meal and urea. DM intake varied between 9.6 and 19.1 kg/d, the crude fibre content between 166 and 270 g/kg DM, the crude protein (CP) content between 111 and 184 g/kg DM, the AA content (N basis) of the CP between 51 and 82%, the unfermentable CP content of the CP between 23 and 49% and the organic matter digestibility between 70 and 79%. The duodenal passage of NAN was 24.2 +/- 2.7 g/kg DM intake, 34.9 +/- 4.1 g/kg apparently digestible organic matter (in total tract, DOM), 43.3 +/- 5.5 g/kg apparently digestible carbohydrates or 4.2 +/- 0.5 g/MJ net energy fat, (y +/- s, n = 90). The value measured for AA-N was 16.8 +/- 2.9 g/kg DM intake, and that for RNA-labelled microbial CP was 146 +/- 26 g/kg DOM. NAN passage (g/kg DM intake) correlated more closely with the duodenal digesta flow rate (DFR) (kg digesta/kg DM intake) as an intrinsic animal factor (r = 0.78) and with the rumen content dilution rate (RDR) (passage of microbial-free organic matter at duodenum/kg BW0.75.h) as a ration dependent factor (r = 0.64) than with the UDP fraction (% of ration CP) (r = 0.50) or other ration parameters. It was concluded that the specific effect of protein concentrates in mixed rations on duodenal NAN yields in lactating dairy cows is lower than hitherto assumed. The duodenal NAN yield of a single feedstuff or ration (g/kg DM) in cows is dependent on animal and feeding factors. The DFR could represents a suitable target for breeding activities.     

The energy metabolism of growing swine in the body weight range of 10-50 kg. 2. Nitrogen and energy metabolism

Investigations were carried out about nitrogen and energy metabolism feeding rations with 17-24 and 44-47% crude protein content on maintenance and growing level to castrated male hybrid pigs of line 150. In growing periods the N deposition amounted to 10 g/animal.d (15 kg live weight), 18 g/animal.d (30 kg LW) and 21 g/animal.d (greater than 40 kg LW) on lower protein feeding level. In experiments with higher protein feeding level the corresponding results were 17, 22 and 22 g N deposition/animal.d. The partial utilization of metabolizable energy for deposition amounted to 70% for the rations with 17-24% protein content and to 59% for the rations with 44-47% protein content, without correlation to the animals development and the alternation in the protein feeding level. The results of regression analysis about maintenance requirement were 814, 775 and 806 kJ metabolizable energy/kg LW0.62.d in trials feeding rations with 17-24% crude protein content as well as 764, 846 and 818 kJ metabolizable energy/kg LW0,62.d in trials feeding rations with 44-47% crude protein content. 1,5-1,8 MJ metabolizable energy were used per MJ protein energy deposition and 1,3-1,4 MJ per MJ fat energy deposition respectively. The energy deposition per kg live weight gain amounted to values between 9 (10 kg LW) and 18 MJ (60 kg LW).     

Urea utilization in growing lambs. 7. NPN- and pure protein-N-utilization at various ages

The utilization quota of NPN and pure feed protein for body protein synthesis was calculated on the basis of N balance experiments with 15N labelled urea with the help of model concepts of a 3-pool model and its mathematical usage. In lambs weighing 13 kg, the efficiency of amino acid and nucleic acid synthesis in the non-amino acid N pool was 64%. This results in a total utilization quota for NPN and pure protein in the ration of 40% and 60%, resp. Lambs weighing 27 kg showed an efficiency in amino acid and nucleic acid synthesis in the non-AA N pool of 77% and in the AA N pool of 60%. The total utilization quota of NPN was 47% and that of pure protein 56%. The pure protein in the ration was thus about twice as well utilized for total protein synthesis and for protein synthesis for crude protein retention as the NPN compounds in the ration.     

Protein and amino acid metabolism in the digestive tract growing young bulls. 1. Flow of bacterial raw protein in the duodenum determined by 2,6-diaminopimelic acid as a marker

The influence of the composition of the rations on the content of diamino pimelic acid (DAP) and N in the bacteria dry matter and on the flow of bacteria crude protein into the duodenum, determined with DAP as marker, was determined on the basis of experimental investigations with young bulls provided with duodenal cannulae and with 28 different rations whose details are described. At a production level corresponding to dry matter intake and a variation range of the crude fibre content of between 11.3 and 29.1% in the DM, a content of N-free extractives between 50.9 and 77.4% in the DM, a content of soluble carbohydrates ibetween 5.3 and 6.4% in the DM, a crude protein content of between 6.4 and 17.1% in the DM and a pure protein content of between 4.9 and 15.5% in the DM, the DAP content of the bacteria DM amounts the 0.350 g 100 g DM +/- 0.090 the N-content of the bacteria DM amounts to 7.37 +/- 1.08 g/100 g DM, there are no relations between DAP- and N-content in the bacteria DM and the content of the individual carbohydrate fractions of the ration, there are positive relations between DAP- and N-content of the bacteria DM, the flow of bacterial crude protein into the duodenum amounts to 133 +/- 14 g/kg truly fermentable organic matter or 130 +/- 14 g/kg apparently digestible organic matter, there is a negative relation between bacteria crude protein at the duodenum (BCPD)/kg truly fermentable organic matter and the crude fibre content of the ration, there is a positive relation between BCPD/kg truly fermentable organic matter and N-free extractives and soluble carbohydrate content as well as the digestibility of the organic matter of the ration, there is no specific influence of the flow rate (kg digesta/kg intake of org. matter) or the dilution rate (g bacteriafree org. matter D/kg LW075/b) on BCPD/kg truly fermentable org. matter, there is a dependence of BCPD/kg truly fermentable org. matter on crude protein concentration in the ration in the concentration range of 6.4-9.0% crude protein in the ration (provided endogenous CP equivalents are used).     

Allantoin excretion of wethers in variations of raw protein and energy administration

216 values of urinary allantoin excretion were received from 8 digestibility trials, which included 48 rations with different protein and energy content. Thus relations between allantoin excretion and food intake and ration composition, respectively, could be evaluated. Additionally variations in N balance were measured, since there is a close relation to allantoin metabolism. Fecal N excretion was elevated with increasing energy intake, but varied only slightly with modified N supply. Urinary N excretion and also N retention increased with higher N intake. On the other hand urinary N losses were reduced with increasing energy supply and part of the saved nitrogen was deposed into the body. There was a distinct increase in allantoin excretion with raised protein intake, when N supply ranged generally low. But with a daily supply of crude protein above 60 to 70 g there was no significant further response in allantoin excretion. Allantoin excretion increased linearly with higher energy supply. Several restrictions for conclusions on the extent of microbial protein production in the digestive tract estimated out of measured allantoin values were discussed.     

Urea utilization in growing lambs. 6. N balance with 15N urea

Lambs of an age of 2 or 4 months and of an average live weight of 14.7 and 27.4 kg resp. received rations consisting of 44% cereals, 46% dried sugar beet pulp, 6% wheat starch, 2% urea and 2% mineral-vitamin mixture. The crude protein content was 17.1 and 15.9% resp. in the dry matter, that of native crude protein 10.6 and 9.4% resp. During a 6-day N balance period 8 and 16 g 15N urea resp. with a 15N excess (15N') of 9.26 and 9.40 atom-% were fed orally instead of commercial feeding urea. There were no significant differences between the two age groups with regard to the digestibility of the organic matter and the crude nutrients. The average N balance of 372 +/- 85 mg/kg LW 0.75/day were in the intermediate range of N retention capacity and accounted for 26 +/- 5% of the consumed N. N retention in per cent. was slightly lower in younger lambs. Projections of urea utilization in a quasi stationary state resulted in an efficiency of the utilization of 33 +/- 4%. The dismembering of the lambs at the end of the main period showed between 0.02 and 0.22 atom-% 15N' in the total N, TCA precipitable N and amino acid N of the meat. At between 0.24 and 0.38 atom-% 15N' they were highest in the heart and jaw muscles. The quota of 15N' amounts found in the total N of the meat were 10.6 +/- 3% of the 15N-intake and 20.1 +/- 5.1% of the 15N' amount remaining in the body. The bones contained 7.7 +/- 1.7% and the fleece 7.9 +/- 3.1% of the 15N'-intake. Generally seen, the total N and urea utilization was slightly lower in younger lambs than in older ones.     

The energy maintenance requirement of growing pigs of different sexes give normal and high protein diets. 2. Experiments in sows

Six animals each out of 12 female fattening hybrids (150 X (L X E] were given rations containing 17 or 45% crude protein resp. 4 periods of growth feeding alternated with 5 periods of maintenance feeding in the live weight range between 33 and 146 kg. The feeding level did not have an influence on the level of digestibility. From the experiments with 17% crude protein in the ration 1004 and from those with 45% crude protein 947, on average 977 kJ metabolizable energy per kg LW0.62 in the maintenance periods and 980 in the growth periods were derived as maintenance requirement of metabolizable energy. These values for maintenance requirement are by 50% higher than those in previous experiments of our work team. In contrast to expectations, energy maintenance requirement did not grow due to the increase of the protein content of the rations. The utilization of metabolizable energy for retention was 73% for rations with a normal protein content and 66% for those with a high protein content. The partial utilization of metabolizable energy for fat retention was ascertained as 83% and as 49% for protein retention by means of multiply regressive evaluation.     

The energy metabolism of growing swine in the liveweight range of 10-50 kg. I. Study design, feed intake and digestibility

Studies of the energy metabolism at maintenance and growth levels after the feeding of rations with a crude protein content of 17-24% and 44-47% resp. were carried out with hybrid pigs of line 150 in the live weight range between 10 and approximately 50 kg. This paper gives information on the methods and the outlay of the experiment and presents results concerning feed intake, live weight development and digestibility. Feed intake increased on average with growing live weight by 30-35 g DM/kg live weight. Feed conversion ranged from 1.2 to 1.8 kg DM/kg live weight gain in the first period and from 2.3 to 3.2 kg DM/kg live weight gain in the last period. The digestibility of the energy in the rations with a crude protein content of between 17 and 24% averaged 80% and that of the rations with a crude protein content of 44-47% averaged 86%. In the course of ontogenetic development the digestibility increased up to about 30 kg LW. The influence of the nutritional level on the level of digestibility was unequal in the experiments. In one experiment a decrease (1% unit) and in two experiments an increase (1-3% units) of the digestibility after the feeding of growth level in contrast to maintenance level could be observed. The change of rations with a varying protein content did not result in an influence on the digestibility level in comparison with the constant feeding of one ration.     

The energy maintenance requirement of growing pigs of different sexes given normal and high protein diets. 3. Experiments in boars

Six fattening boars each, hybrids of line 150(150 X (L X E] received rations with 17 and 45% crude protein. In the live weight range of 36 to 167 kg, 5 periods of growth feeding alternated with 4 periods of maintenance feeding. Compared with maintenance level the nutrition level of 2.7 did not have an influence on digestibility. Nitrogen retention was only insignificantly influenced by the level of protein supply. The maintenance requirement of the animals used was by 50% higher than in previous experiments made by our work team. On average it amounted to 1,017 KJ metabolizable energy per kg LW0.62, i.e. to 1,063 for those animals fed with rations containing 17% crude protein and to 986 for those animals receiving 45% crude protein in their rations. The utilization of metabolizable energy for energy retention amounted to 75% for rations with 17% crude protein and to 70% for rations with 45% crude protein. The partial utilization of metabolizable energy for fat retention was ascertained as 90% and for protein retention as 53% by means of multiply regressive assessment.     

The substitution of lysine supplemented high protein wheat for protein feeds during the rearing and laying periods of hens. 8. Nitrogen excretion and true amino acid digestibility as an effect of various lysine levels and successive laying periods]

Digestibility trials were performed with laying hens receiving 3 types of rations containing equal proportions of the same dietary components. The percentage of high-protein wheat in these rations was 74%. Ration I was supplemented with 0.12% lysine while 0.06% lysine was added to ration II; ration III remained unsupplemented. The crude protein content of rations 1 to 3 was 16.1%, 16.5% and 16.6%, respectively. The corresponding lysine percentages were 0.66, 0.62 and 0.56. Studies were made to investigate the influence of different lysine levels on the rate of N excretion and various amino acid data. These studies were carried out during two successive laying periods. Only random differences between the data for urinary N excretion and N balances per kg liveweight were obtained in the two laying periods and for the different lysine levels. The true lysine digestibility was significantly lower in the poor-lysine ration as compared with the ration with 0.66% lysine. Moreover, the absorptive capacity for thio-amino acids is influenced by the lysine level of the ration. The proportion of lysine contained in faecal crude protein increased with the decreasing lysine content of the ration. Similarly, the total number of amino acids present in faecal crude protein increased with the declining supply of lysine. These findings suggest that relatively more NPN compounds are excreted in the faeces if adequate amounts of amino acids are supplied rather than when one amino acid is deficient.     

Urea utilization of growing lambs. 2. Growth experiments

In two growth experiments with 30 lambs per group the influence of urea (1-2% of the ration) and straw (20-30% of the ration) on the performance was studied under conditions of intensive fattening. The content of native crude protein in the rations varied between 10.1 and 18.4% of the DM. In experiment 1 the lambs of the two groups which received mixed feed for fattening lambs without urea on average consumed with 1.02 and 1.11 kg DM resp., 696 and 757 EFUcattle resp. and 173 and 189 g crude protein resp. per animal and day. The groups with wheat or barley and urea consumed 1.06 and 0.96 kg DM resp., 714 and 627 EFUcattle resp. and 209 and 155 g crude protein resp. Their weight gain of 247 g/animal and day was 24% and that of 230 g resp. 26% higher than that in the control groups without urea. The lowest dry matter intake (0.91 and 0.82 kg resp.) was shown by the animals of the groups which received wheat or barley without urea. In the second experiment the control group achieved an average daily weight gain of 327 g at an expenditure of 2.24 kEFUcattle/kg weight gain. Despite a partly higher dry matter intake, the daily EFUcattle intake was between 12.2 and 24.5% lower in the straw groups and energy expenditure increased between 12.0 and 27.8%. Urea supplements of between 1 and 2% improved dry matter, EFUcattle and crude protein intake and thus weight gain.     

Physiologic and nutritional studies in pigs with ileorectal anastomoses. 3. Nitrogen retention and utilization following energy an electrolyte supplementation

In order to guarantee an equally good development of ileorectostomized pigs (IRA) used for the determination of precaecal protein digestibility and the absorption of amino acids as for intact animals (INT), the supplementation of their rations with easily soluble carbohydrates and minerals is necessary. The effects of these supplements on live weight development, nitrogen balance and N utilization level were the subject of the assessment of 21 rations with 129 and 117 balance measuring resp. with growing IRA and INT pigs. Without any supplementation of the rations the N balances of the IRA pigs showed significantly lower and partly negative N balances and N utilization levels in comparison to the INT pigs. The combined supplement of easily soluble carbohydrates (100 g/kg DM intake) and 300 ... 400 ml electrolyte solution per day (approximately 1 ... 1.3 g additional Na) resulted in N balances almost equal to those of INT pigs. The supplement of both electrolyte solution and NaHCO3 (approximately 2 g Na per animal and day additionally) to a barley + lysine ration resulted in a significant increase of the N balance and N utilization in IRA pigs of a live weight between 120 and 140 kg in contrast to the control period. A supplement of carbohydrates to a ration consisting of barley + fish meal + grass meal and electrolyte supplements of 400 ml per animal and day only resulted in significantly higher N balances and N utilization levels in the live weight range up to 70 kg in comparison to the control periods, which then corresponded to those of INT pigs. There was no essential influence of carbohydrate supplementations on pigs of more than 70 kg live weight. The postileal digestibility of the crude carbohydrates (CC) of 14 rations calculated from the difference between total digestibility (faecal analysis) and precaecal digestibility (analysis of the ileal chyme of IRA pigs) showed that between 40 and 100 g (70 g on average) out of the 780 g CC per kg DM consumed disappear in the large intestine. These studies show that in the testing of concentrates and mixed feed rations the supplementation of 100 g easily soluble carbohydrates/kg DM intake should be sufficient to guarantee a normal development of IRA pigs. In addition, an oral supply of 1 to 2 g sodium in the form of electrolyte solution exceeding the requirement of INT pigs is necessary as this supplementation significantly improves the N retention of IRA pigs even heavier than 100 kg.     

The energy requirement of heifers. 4. Comparison of the digestibility and rumen physiologic parameters in heifers and full-grown sheep

In 159 comparative studies with fully grown sheep and heifers of the digestibility and of rumen physiologic values at a variation of the feed ration in the crude fibre content between 112 and 318 g, in the crude protein content between 94 and 194 g and in the content of nitrogen free extractive between 484 and 641 g/kg DM is provided that the digestibility of energy in heifers was, on average, 4 digestibility units lower than in sheep. The corresponding values for the digestibility of crude protein and crude fibre are 12 and 3.5 digestibility units. Due to the lower methane energy excretion of the heifers the difference at the level of metabolizable energy is reduced to 1.5% of the gross energy. The level of the differences in digestibility is influenced by the development of the young cattle and the composition of the rations. In young cattle of the live weight range between 100 and 150 kg the digestibility of the energy is 6-8 units lower than in sheep. A higher crude fibre content in the ration diminishes the difference in the digestibility of energy and the nutrients between the two animal species.     

Effects of rumen-protected methionine in a low protein ration on metabolic traits and performance of early lactating cows as opposed to rations with elevated crude protein content

A 5‐week experiment with 24 multiparous early lactating Brown Swiss cows was conducted to investigate the effects of supplementary rumen‐protected methionine in conjunction with dietary protein reduction on metabolism and performance after 1 week of control measurement. Three rations containing 175, 150 and 125 g of crude protein/kg feed dry matter were supplemented with methionine. The fourth ration, also only containing 125 g of crude protein/kg dry matter, remained unsupplemented. The four treatment groups had a similar metabolic supply of other essential amino acids, protein and energy, as calculated by various approaches. The two low protein rations were, however, slightly deficient in ruminally degraded protein. Treatment effects remained low on feed intake, forage meal pattern, milk yield and fat as well as lactose content. In contrast, the content and yield of milk protein significantly declined only in the unsupplemented low protein ration relative to the initial value. Compared with this ration, the decline in milk protein yield was clearly delayed in the supplemented low protein ration. Blood plasma methionine tended to be reduced without supplementation and to be increased with additional methionine. Supplementation of methionine reduced other plasma amino acids. Plasma insulin, glucose, lactate, ketone bodies and aspartate amino transferase activity indicated a certain liver stress and a somewhat elevated energy requirement with high and particularly with low protein content (when unsupplemented). Methionine improved metabolic protein utilization, followed by the lowest plasma, urine and milk urea levels in the supplemented low protein diet. In conclusion, no major adverse effects were assessed under the conditions tested. Supplementation of methionine may nevertheless be useful in rations with particularly low protein content fed to early lactating cows in order to prevent negative long‐term effects which were only visible here as trends.     

The energetic utilization of rations with dried concentrates, potatoes, sugar beets, apple pectin and cane sugar by growing, intact and ileorectostomized swine. 1. Results in swine with ileorectal anastomoses

Rations with dried feedstuffs and rations with between 30 and 50% raw potatoes in the dry matter as well as steamed potatoes and sugar beets, sucrose and apple pectin were tested in measurings of the total metabolism in growing pigs with ileo-rectal anastomoses. The prececal digestibility of the energy of the rations ranged between 42% (rations with raw potatoes) and 79% (rations with sucrose). The digestibility of the rations with a 50% quota of steamed potatoes was better by 30%--units than that of rations with raw potatoes. In addition to crude nutrient digestibility, data are given on the digestibility of starch, water soluble carbohydrates and pectin. The wide variation in the N retention of 6-25 g/animal.day can only be partly connected with energy retention. Urine energy amounted to between 2.5 and 5% of gross energy. The average utilization of metabolizable energy amounted to 69.4%. A connection is to be seen with the value of energy maintenance requirement of 646 kJ retention energy/kg LW0.62.d.     

Nutrition physiology effects of dietary fats in rations for growing pigs. 5. Effects of soy bean oil and lard on protein retention in piglets

In two experiments with 30 and 26 castrated male pigs of the German Landrace breed, weight range 15-30 kg, the influence of isoenergetic changes in the carbohydrate and fat fractions of the diet were examined. The effect of the addition of soya oil (SO) and lard (LA) to the diet on the utilization of protein and on the blood urea concentration was also examined. The apparent digestibilities of the crude nutrients and energy were determined using different methods. The following were examined: experiment I: ration I (control), ration II (+7% SO), ration III (+7% LA) experiment II: ration I (control), ration II (+2% SO), ration III (+2% SO + 5% LA), ration IV (+7% LA) In all experiments the animals were fed a similar amount of digestible crude protein of constant quality at constant ME-intake. In both experiments the apparent digestibility of crude protein in the groups with 7% added fat was 4% higher (p less than 0,05) than in the corresponding control groups. The apparent digestibility of crude fat in experiment I and II (in groups II and III and in groups III and IV, respectively) was approximately 87%, when calculated on the basis of faecal fat which was determined by a simple ether extract procedure. When the faeces was treated with HCl before determination, these values for experiment I and II were approximately 6% (p less than 0,001) and 1% (NS) lower, respectively. In both experiments the utilization of protein and the blood urea concentration were not significantly influenced by the amount or form of fat included in the rations.     

Effect of the content of crude plant protein in the ration on the utilization of urea in dairy cattle. 2. 15N-urea metabolism

The metabolism of 15N-urea in the rations of dairy cows was investigated in dependence on the crude protein content of the rations. With energy concentration remaining unchanged, the rations contained 10.7 (I), 13.7 (II) and 17.1 (III)% plant crude protein and, after the supplementation of 150 g urea per animal and day, a total of 13.8, 16.7 and 20.2% crude protein in the dry matter. The urea was intraruminally infused during the feeding in the morning and the evening. In the morning feeding of each 1st measuring day it was labelled with 27.5 atom-% 15N-excess (15N'). The degree of labelling with 15N' of the N-fraction of rumen fluid, contents of the duodenum, faeces and milk, precipitable with trichloric acetic acid (TCA) decreased with the rising protein level of the ration. This effect was bigger than could be expected considering the low 15N'-quota in the total-N of the ration. In the sequence I ... III, 52.7, 32.2 and 30.6% of the 15N'-amount taken in passed the duodenal re-entrant cannula in TCA-precipitable form within 72 hours after the 15N-application. 33.3, 21.9 and 22.6% were apparently absorbed in the intestines as TCA-precipitable N within 120 h after the 15N'-application. In the same period 31.7, 43.1 and 72.8% of the 15N' taken in were excreted in urine. 12.3, 9.6 and 5.8% of the applied 15N' were found in milk protein. One can conclude that the utilisation of urea-N decreases with the rising level of crude protein in the ration and that, however, urea-N is still biochemically utilised when there is an excess of plant-N in the ration.