Effect of dietary amino acids and metabolisable energy on the performance of broilers kept at high temperatures

Increasing dietary metabolisable energy (ME) at particular amino acid: ME ratios significantly improved growth and food utilisation of broilers kept at moderate (18 to 26 degrees C) and high (25 to 35 degrees C) ambient temperatures during the finishing period from 22 d of age. The optimum amino acid: ME ratio varied with dietary ME concentration in the hot, but not in the moderate environment. Relatively greater increases in food intake and growth rate occurred in the hot environment when dietary ME was increased and the amino acid: ME ratio was reduced. The minimum rate of food intake did not coincide with the period of maximum temperature. Increasing the dietary protein at particular ME concentrations had little or no effect on the food intake and growth rate of birds kept at high temperatures. Supplementation with dietary fat had no beneficial effect on performance at high temperatures. The rectal temperatures of birds in the hot environment increased with age and, towards the end of the finishing period, when higher energy diets were fed.     

Endogenous losses of energy and amino acids in birds and their effect on true metabolisable energy values and availability of amino acids in maize

1. Endogenous losses of amino acids (EAAL) and energy (EEL) were determined in unfed adult cockerels. The intercepts of linear regression analysis were determined using 44 birds precision-fed on maize. During the experimental period (48 h), excreta of birds were collected, and the samples of maize and the excreta were dried, ground and assayed for gross energy and amino acids. 2. The EAAL and EEL in unfed cockerels influenced true available amino acid (TAAA) values. Therefore, the intercept of regressions showed an increase in TAAA values of maize. 3. The results indicated that there was no significant difference between the data obtained for EEL from the unfed birds and from regression analysis so, the figure from regression analysis could be used for calculating the true metabolisable energy (TME) value of maize. 4. The calculated EAAL from regression analysis caused an increase in the TAAA value in maize. The amounts of metabolic and endogenous amino acid excretions varied in voided excreta from unfed birds. These differences would be related to genetics, age, sex and environmental temperatures.     

Comparison of two direct bioassays using 3-week-old broilers to measure the metabolisable energy of diets containing cereals high in fibre: differences between true and apparent metabolisable energy values

1. Nitrogen-corrected apparent and true metabolisable energy contents (AMEN and TMEN) of 12 diets, containing different amounts of maize, wheat, barley and rye, barley with beta-glucanase and maize with 0.05 g/kg guar gum were measured using 3-week-old male broilers. 2. The AMEN method involved: 4 d of dietary adaptation, 24 h of starvation, 54 h of ad libitum feeding, 24 h of starvation and daily total droppings collection. TMEN was measured after a 48 h starvation period followed by 2 d of tube-feeding two doses of 15 g of the diets and quantitatively collecting all the droppings after 48 h of starvation. The endogenous energy losses (EELN) were measured after tube-feeding 8 chickens with 30 g of glucose, also over 2 d. 3. The results show that a significant interaction exists between the nature of the diets and the method used to measure metabolisable energy. Differences between TMEN and AMEN values ranged from 1.03 to 1.98 MJ/kg dry matter. These differences were positively correlated with the total pentosan contents of the diet (r = 0.94), the natural logarithm of the viscosities of the water extracts (r = 0.87), the sum of the contents of total pentosans and total beta-glucan (r = 0.85), the calculated total non-starch polysaccharide contents (r = 0.79), the neutral detergent fibre contents (r = 0.76) and the total beta-glucan contents (r = 0.70). Furthermore, a significant interaction was found between diets and the method used to derive lipid digestibility. The differences between apparent and true lipid digestibility ranged from 0.05 percentage points for the wheat diet to 0.20 percentage points for the rye diet. 4. From the results of this trial, it appears that TMEN overestimates the energy value of high fibre diets.     

Relationship between digesta transit time and apparent metabolisable energy value of wheat in chickens

1.?This study tested the hypotheses that: (a) apparent metabolisable energy (AME) values and whole tract transit time (WTTT) were related, and that (b) the relationship between AME and WTTT differed between male and female Ross broiler chickens.

2.?Enzyme products with xylanase activity were added to a basal diet to provide 4 dietary treatments comprising control (no enzyme), Avizyme 1300 (1 kg/tonne), Kemzyme W1 (1 kg/tonne), and Bio-Feed Wheat CT (200 g/tonne). The basal diet comprised (in g/kg), 800 wheat, 155 casein, 20 dicalcium phosphate, 11 limestone, 7 D,L-methionine, 2 vitamin and mineral premix, 3 sodium chloride and 2 choline chloride (60%).

3.?AME values for diets were determined in a 7-d energy balance study commencing when chickens were 21 d of age. WTTT was the time elapsed (in min), from time of administration by oral gavage of 200 mg ferric oxide in a gelatine capsule, to time of first observation of the distinctive red colouration in droppings.

4.?The mean AME value for the wheat was high (15·7 MJ/kg dry matter) and ranged from 14·4 to 16·3 MJ/kg dry matter for individual birds. Mean WTTT was 206 min and ranged from 105 to 429 min. AME and WTTT were unaffected by enzyme addition to the diet, and the interaction between diet and gender was not significant.

5.?There was a significant but weak positive relationship between AME and whole tract transit time, with AME increasing by 2·2 kJ/min. This relationship was unaffected by gender of the chicken.     

Effects of wheat variety and specific weight on dietary apparent metabolisable energy concentration and performance of broiler chicks

1. This study used 4 wheat cultivars (Brigadier, Chaucer, Consort, Reaper) from three locations (Crossnacreevy, C; Downpatrick, D; Limavady, L), which had given rise to differences in wheat specific weight (SW), to examine the relationships between apparent metabolisable energy (AME) concentration, broiler performance and wheat SW. 2. The diets contained (g/kg): wheat 744, casein 142, blended vegetable fat 50, dicalcium phosphate 22, potassium bicarbonate 10.8, sodium bicarbonate 7.5, arginine 5, methionine 2, binder 8, trace minerals/vitamins 7.2, titanium dioxide 1.5. The diets were heat-treated (80 degrees C for 2 min) prior to pelleting (3 mm die). 3. SW ranged from 63 to 77 kg/hectolitre (hl), averaging 66, 69 and 76 kg/hl at D, C and L, respectively. In vitro viscosity of the wheat samples ranged from 5.2 to 17.5 cps and thousand grain weight (TGW) from 33.4 to 47.3 g. Mean TGW was similar at C and D (38.7, 37.0 g) but higher at L (43.1 g). In vitro viscosity was similar at C and L (11.2, 10.2 cps) but somewhat higher at D (14.4 cps). Crude protein (6.25 N) ranged from 116 to 147 g/kg and tended to be higher at D. Starch, which ranged from 612 to 656 g/kg, was least at D (617 g/kg) and greatest at L (641 g/kg). 4. Crude protein, crude fibre and total non-starch polysaccharide (NSP) were negatively correlated with SW, the R2 being respectively 0.38 (P<0.05), 0.16 (NS) and 0.45 (P<0.05). TGW and starch concentration were positively correlated with SW (R2=0.70, 0.44, respectively). There was a weak (NS) negative relationship (R2=0.19) between in vitro viscosity and SW. For both TGW and in vitro viscosity, correlations improved when variety was taken into account (R2=0.95, 0.92, respectively). 5. There were no significant effects of variety on dry matter (DM) intake or live weight gain (LWG). Gain: food was significantly higher (P<0.05) for Consort than for the other three varieties and the metabolisable energy ratio (ME:GE) just failed to attain significance (P=0.062). Calculated wheat AME (MJ/kg DM) was significantly (P<0.05) higher for Consort than for the other three wheats. There was a good correlation (R2=0.49) for the total data set between gain:food and ME:GE. In vivo viscosity varied from 13.6 to 28.6 cps for individual treatments and was significantly affected by variety (P<0001). 6. Although there were no significant differences in DM intake or LWG due to site the values for L (SW 76) were 6 and 5% lower, respectively, than for D (SW 66). Gain:food was lower (P<0.05) for C (SW 69) than for D. ME:GE, wheat AME and ME:gain were not significantly different between sites. 7. There was a weak (R2=0.18) positive relationship between ME:GE and SW corresponding to a 2.5% increase in energy value for a 10 kg/hl increase in SW and no relationship between gain:food and SW. When variety was taken into the regression the slope was similar but R2 increased to 0.82. 8. ME:GE and wheat AME concentration were negatively correlated with wheat in vitro viscosity (R2=0.64, 0.55, respectively). 9. It was concluded that in vitro viscosity appears to provide a better basis than SW for prediction of the nutritive value of wheats of unknown variety. If the variety is known then SW could be used to predict energy value. However, the effect of quite a large change in SW (10 kg/hl) was relatively small.     

Interactions between fats of differing chemical content: apparent metabolisable energy values and apparent fat availability

1. Tallow (A) and rape oil (E) were obtained for evaluation. They were blended in the ratios A95:E5, A90:E10 and A80:E20. The three blends together with the two pure fats were each included at 40, 80 and 120 g/kg into a basal diet. 2. The experimental diets were evaluated for apparent metabolisable energy corrected to zero nitrogen retention (AMEN MJ/kg) and apparent fat availability (g/kg) using 6 replicates of a cage of two male broiler chicks 14 d old and 8 replicates of a cage of one Rhode Island cross cockerel approximately 1 year old. Diets were fed for 72 h then removed for 24 h. This was followed by a 48 h period when food was available ad libitum and a further 24 h of starvation. A total collection of excreta was undertaken each 24 h for the latter 72 h period. 3. Evaluation of AMEN and apparent fat availability for the individual fat blends was achieved through both linear and quadratic regression. 4. Synergism, as demonstrated by a higher determined than calculated AMEN value, was detected with fat blends fed to chicks but not cockerels and only at rates of inclusion beyond 80 g/kg. 5. No consistent differences between AMEN determined through calorimetry or AME determined with reference to apparent fat availability multiplied by fat gross energy were detected.     

Effects of xylanase supplementation on the apparent digestibility and digestible content of energy, amino acids, phosphorus, and calcium in wheat and wheat by-products from dry milling fed to grower pigs

Wheat by-products are feedstuffs that vary in nutritional value, partly because of arabinoxylans that limit nutrient digestibility. Millrun is a byproduct from dry milling wheat into flour and contains varying amounts of the bran, middlings, screening, and shorts fractions. The digestible nutrient content of mill-run is not well known. Effects of xylanase supplementation (0 or 4,000 units/kg of diet) on energy, AA, P, and Ca digestibilities were studied in a wheat control diet and 5 diets containing 30% of a by-product (mill-run, middlings, shorts, screening, or bran) in a 2 x 6 factorial arrangement of treatments. The wheat control diet was formulated to contain 3.34 Mcal of DE/kg and 3.0 g of standardized ileal digestible Lys/Mcal of DE. Diets contained 0.4% chromic oxide. Each of 12 ileal-cannulated pigs (32.5 +/- 2.5 kg) was fed 6 or 7 of 12 diets at 3 times the DE requirement for maintenance in successive 10-d periods for 6 or 7 observations per diet. Feces and ileal digesta were each collected for 2 d. Xylanase tended to increase (P < 0.10) ileal energy digestibility by 2.2 percentage units and the DE content by 0.10 Mcal/kg of DM and increased (P < 0.05) ileal DM digestibility by 2.8 percentage units; a diet x xylanase interaction was not observed. Xylanase increased (P < 0.05) total tract energy and DM digestibilities and the DE content. A diet x xylanase interaction was observed; xylanase increased (P < 0.05) total tract energy digestibility of the millrun diet from 72.1 to 78.9%, DE content from 3.19 to 3.51 Mcal/kg of DM, and DM digestibility from 71.5 to 78.6%. Diet affected (P < 0.05) and xylanase improved (P < 0.05) digestibility and digestible contents of some AA in diets and by-products, including Lys, Thr, and Val. Xylanase increased (P < 0.05) Lys digestibility by 13.8, 5.0, 5.2, 6.0, and 14.1 percentage units in millrun, middlings, shorts, screening, and bran, respectively. Diet affected (P < 0.01) total tract P and Ca digestibilities. Xylanase increased (P < 0.05) digestible P and Ca contents. In summary, nutrient digestibility varies among wheat by-products. Millrun contained 2.65 Mcal of DE/kg of DM, which xylanase increased to 3.56 Mcal of DE/kg of DM. Xylanase improved nutrient digestibility and DE content in wheat by-products; and the extent of improvement depended on the by-product. Xylanase supplementation may maximize opportunities to include wheat byproducts in swine diets and ameliorate reductions in nutrient digestibility that may be associated with arabinoxylans.     

Effect of dietary energy concentration on the response of laying hens to amino acids

1. A hypothesis, that the optimum amino acid concentration in the diet is not directly proportional to the dietary energy concentration, but changes in inverse proportion to the change in food intake resulting from a change in energy concentration, was tested in three experiments.

2. Response experiments involving the amino acids methionine, lysine and isoleucine were conducted, in each case at three dietary energy concentrations, using a diet dilution and blending technique, thereby ensuring a constant ratio between background amino acids and the first‐limiting amino acid in all diets, and also keeping the ratio of amino acids to energy constant as energy varied.

3. A common response curve relating egg output (g/bird d) to amino acid intake (mg/bird d) for each amino acid, fitted by means of the Reading Model, adequately described the response at each of the dietary energy contents. This implies that energy does not influence egg output directly, but only indirectly through its effect on food intake and hence on amino acid intake.

4. Both amino acid and energy concentration significantly influenced food intake. Energy intake was not constant over all dietary energy concentrations, being lower at low energy levels and higher at high energy concentrations.

5. It is concluded that amino acid requirements should not be stated either as percentages or as ratios with energy. Optimum amino acid intakes and energy concentrations should be calculated; the expected food intake should then be predicted, after which the appropriate concentration of nutrients in the diet can be determined.     

Development of a model to predict dietary metabolizable energy from digestible energy in beef cattle

Understanding the utilization of feed energy is essential for precision feeding in beef cattle production. We aimed to assess whether predicting the metabolizable energy (ME) to digestible energy (DE) ratio (MDR), rather than a prediction of ME with DE, is feasible and to develop a model equation to predict MDR in beef cattle. We constructed a literature database based on published data. A meta-analysis was conducted with 306 means from 69 studies containing both dietary DE and ME concentrations measured by calorimetry to test whether exclusion of the y-intercept is adequate in the linear relationship between DE and ME. A random coefficient model with study as the random variable was used to develop equations to predict MDR in growing and finishing beef cattle. Routinely measured or calculated variables in the field (body weight, age, daily gain, intake, and dietary nutrient components) were chosen as explanatory variables. The developed equations were evaluated with other published equations. The no-intercept linear equation was found to represent the relationship between DE and ME more appropriately than the equation with a y-intercept. The y-intercept (−0.025 ± 0.0525) was not different from 0 (P = 0.638), and Akaike and Bayesian information criteria of the no-intercept model were smaller than those with the y-intercept. Within our growing and finishing cattle data, the animal’s physiological stage was not a significant variable affecting MDR after accounting for the study effect (P = 0.213). The mean (±SE) of MDR was 0.849 (±0.0063). The best equation for predicting MDR (n = 106 from 28 studies) was 0.9410 ( ± 0.02160) +0.0042 ( ± 0.00186) × DMI (kg) – 0.0017 ( ± 0.00024) × NDF(% DM) – 0.0022 ( ± 0.00084) × CP(% DM). We also presented a model with a positive coefficient for the ether extract (n = 80 from 22 studies). When using these equations, the observed ME was predicted with high precision (R² = 0.92). The model accuracy was also high, as shown by the high concordance correlation coefficient (>0.95) and small root mean square error of prediction (RMSEP), <5% of the observed mean. Moreover, a significant portion of the RMSEP was due to random bias (> 93%), without mean or slope bias (P > 0.05). We concluded that dietary ME in beef cattle could be accurately estimated from dietary DE and its conversion factor, MDR, predicted by the dry matter intake and concentration of several dietary nutrients, using the 2 equations developed in this study.     

Effect of dietary soybean oil and soybean protein concentration on the concentration of digestible amino acids in soybean products fed to growing pigs

An experiment was conducted to measure the effect of adding soybean oil to soybean meal (SBM) and soy protein concentrate (SPC) on apparent (AID) and standardized (SID) ileal digestibility of CP and AA by growing pigs. A second objective was to compare AID and SID of AA in a new high-protein variety of full fat soybeans (FFSB) to values obtained in other soybean products. Commercial sources of FFSB (FFSB-CV), SBM, and SPC, and of a new high-protein variety of FFSB (FFSB-HP) were used in the experiment. Four diets were prepared using each soybean product as the sole source of CP and AA in 1 diet. Two additional diets were formulated by adding soybean oil (7.55 and 7.35%, respectively) to the diets containing SBM and SPC. A nitrogen-free diet was also used to measure basal endogenous losses of CP and AA. The 2 sources of FFSB were extruded at 150 degrees C before being used in the experiment. Seven growing barrows (initial BW = 26.2 kg) were prepared with a T-cannula in the distal ileum and allotted to a 7 x 7 Latin square design. Ileal digesta were collected from the pigs on d 6 and 7 of each period. All digesta samples were lyophilized and analyzed for DM, CP, AA, and chromium, and values for AID and SID of CP and AA were calculated. The addition of oil improved (P < 0.05) the SID of most indispensable AA in SBM and SPC. The SID for 6 of the indispensable AA in FFSB-HP were greater (P < 0.05) than in FFSB-CV, and the SID for all indispensable AA except Met was greater (P < 0.05) in FFSB-HP than in SBM. However, the SID for most AA in FFSB-HP was similar to SBM with oil and SPC, but these values were lower (P < 0.05) than in SPC with oil. In conclusion, the addition of oil improved the SID of most AA in SBM and SPC fed to growing pigs, and the SID of AA in FFSB-HP were greater than in SBM and similar to the SID of AA in SBM with oil and in SPC.     

Effect of added soyabean oil and dietary energy on metabolisable and net energy of broiler diets

1. The ‘extra caloric’ effect of added soyabean oil, as reflected in improved body weight gain, food utilisation, metabolisable energy or net energy deposition in the body was determined.

2. Two diets were formulated to contain 12.1 MJ/kg, one with no added fat and the second with 30 g/kg soyabean oil. Addition of oil improved body weight gain by 6.9% (P< 0.05). Two other diets were formulated to contain 13.0 MJ/kg, one with 30 and one with 60 g/kg added soyabean oil bringing the total fat in the high energy, high fat diet to 84 g/kg. Addition of oil in this case improved weight gain by only 3^.4% (ns). Addition of soyabean oil increased the apparent digestibility of total dietary fat and reduced that of starch.

3. The effect of soyabean oil supplementation on mash diets at both energy concentrations or to the pelleted diet (formulated to contain 12.1MJ) on AME_n was consistently positive although not significant. Addition of soyabean oil improved net energy deposition in the body by 17% within the 12.1 MJ/kg diets, (30 g/kg soyabean oil addition) (P< 0.05), but was reduced by 2% (ns) within the 13.0 MJ/kg diets (60 g/kg soyabean oil addition).

4. Supplementing a pelleted diet formulated to contain 12.1 MJ/kg, with 30 g/kg soyabean oil, improved food utilisation (P< 0.05). The ‘extra caloric’ effect of added soyabean oil, defined as the beneficial effect of the oil above that predicted from its energy value, varied according to the parameter chosen to express this effect and was influenced by the concentration of added soyabean oil and the dietary energy.     

Interactions between dietary crude protein and essential amino acid intake on performance in broilers

1. The effect of diets with increasing concentrations of crude protein at either fixed essential amino acid concentrations or at fixed essential amino acid:dietary crude protein ratios on performance was examined in 1- to 4-week-old male Cobb chicks. Increasing crude protein intakes at constant essential amino acid concentrations was carried out at two dietary energy contents. 2. Increasing crude protein resulted in a linear decrease in feed intake while weight gain and feed efficiency changed quadratically with a smaller positive effect at the highest crude protein intakes. Feed intake decreased and feed efficiency increased with higher dietary energy and interactions between protein and energy were significant. Abdominal fat content and the efficiency of protein retention decreased with increasing dietary protein intake. 3. Using constant essential amino acid:crude protein ratios at increasing crude protein intakes resulted in (Trial 3) feed intake, weight gain and feed efficiency all increasing before reaching a plateau. Abdominal fat decreased with protein intake and the efficiency of protein retention was quadratic, decreasing at the higher protein intakes. 4. Multiple regression analysis of the results of the three trials indicated that partition of energy intake into maintenance, fat-free tissue growth, fat and the energy required to transform protein intake in excess of retention explained more than 98% of variation. 5. It is proposed that broiler performance at the lower protein intakes was limited by either non-essential amino acid (Trials 1 and 2) or essential amino acid (Trial 3) intake whereas at high protein intakes the decreased efficiency of amino acid utilisation after growth requirements are fulfilled resulted in poorer performance.     

饲料原料的变异及用近红外光谱仪检测可消化氨基酸与代谢能

本文介绍了同种饲料原料不同批次间营养价值的差异及实测饲料代谢能和可消化氨基酸的程序、近红外(NIRS)数据库及标准曲线的建立、NIRS快速测定值与实际动物体内试验测定值的比较等内容。     

净能体系和可消化氨基酸体系在养猪生产中的应用

<正>目前,畜牧业中能量饲料是成本最高的一种饲料,如何提高能量的利用率以及减少能量的浪费已成为畜牧行业中亟待解决的问题。净能体系最早应用于奶牛的日粮配制当中,在单胃动物中一直沿用着消化能和代谢能体系,但消化能和代谢能体系有高估蛋白质和纤维能值的趋势,低估了脂肪和淀粉的能值(Noblet,     

A comparative study between mature ostriches (Struthio camelus) and adult cockerels with respect to true and apparent metabolisable energy values for maize,barley, oats and triticale

1. In three successive trials with cockerels and mature ostrich males the apparent and true metabolisable energy values, corrected for nitrogen retention (AME_n and TME_n) were determined by a balance method for malting barley, oats, triticale and yellow maize. All these ingredients were used as sole dietary components with the exception of triticale for ostriches which was diluted with 440 g/kg lucerne meal. The balance trial lasted for 5 d after an adaption period of 7 d for ostriches, and 3 d after an adaption period of one day for cockerels.

2. AME_n values for cockerels of malting barley, oats, triticale and maize were 11.6, 10.48, 11.44 and 14.42 MJ/kg respectively. Significantly higher values of 14.21, 12.65, 12.60 and 14.89 MJ/kg were determined for malting barley, oats, triticale and maize for ostriches.

3. TME_n values determined by regression yielded values in ostriches of 13.92, 12.27, 13.21 and 15.22 MJ/kg for malting barley, oats, triticale and maize respectively. The corresponding TME_n values in cockerels were 11.33, 10.63, 11.82 and 14.07 MJ/kg.

4. The ostrich is capable of utilising fibre more efficiently than poultry. The higher energy values observed for the various ingredients also indicated that the non‐starch polysaccharides such as ß‐glucans and arabinoxylans in the more fibrous energy sources had little if any effect on the available energy of these ingredients as found with poultry.

5. The potential of ostriches to utilise the more fibrous energy sources like barley, oats and triticale allows for their economical use in diet formulation. This possibility may result in markedly lower food costs for ostriches.     

更新现代瘦肉型猪的日粮赖氨酸水平及其与净能比例以提高生产性能

为了追求最大的生产效率,养猪业不断地通过遗传育种改良猪品种。与十多年前相比,今天的现代猪瘦肉率更高,吃得更少、长得更快,因此,其营养需要也发生了变化。而NRC(1998)的推荐需要量仍被广泛地应用于生产。最近十多年的许多研究表明,现代瘦肉猪的赖氨酸需要量比NRC(1998)推荐值高20%～30%。按理想蛋白模式,更新现代瘦肉猪的氨基酸需要量及其与能量比例,可充分发挥现代瘦肉型猪的生产潜能。     

Effect of apparent ileal digestible lysine to energy ratio on performance of finishing pigs at different dietary metabolizable energy levels

A study with a total of 96 crossbred barrows and gilts fed ad libitum in a body weight range of 56-110 kg was carried out in order to investigate whether the optimum ratio of apparent ileal digestible lysine : energy (ME) depends on the energy density of the diet. Dietary treatments were ratios of 0.34, 0.42, 0.50 and 0.58 g digestible lysine/MJ ME either at an energy density of 13 or 14 MJ ME. Body weight gain as well as feed and ME conversion rate were improved when lysine : ME ratio increased from 0.34 to 0.50, whereby all parameters showed a significant ratio x sex interaction. Feed intake and feed conversion rate were higher at a dietary energy density of 13 MJ ME than at an energy density of 14 MJ ME but energy density did not influence daily growth rate, ME intake and ME conversion rate. Fat area above eye muscle and meat : fat ratio were lower and eye muscle area and lean percentage were higher at a ratio of 0.42 compared with a ratio of 0.34. Daily feed intake, body weight gain, feed conversion rate and parameters of fatness were higher in barrows than in gilts. Conversely, gilts had higher eye muscle area and lean percentage. Optimum ratio for body weight gain, feed and ME conversion rate calculated by exponential regression analysis were 0.42-0.43 in barrows. In gilts, feed and ME conversion rate were optimized at a ratio of 0.53 and 0.54. Because growth showed a linear response to increasing digestible lysine : ME ratios, optimum ratio for daily gain in gilts is considered to be at least 0.58.