Search

Two experiments were conducted to determine DE and ME and the apparent ileal digestibility (AID) and the standardized ileal digestibility (SID) of CP and AA in corn and corn coproducts (high-fat corn germ [HFCG], corn bran, liquid corn extractives [LCE], and a mixture of corn germ meal and LCE [CGM-LCE]) fed to growing pigs. In Exp. 1, 40 growing barrows (initial BW: 33.4 ± 5.77 kg) were housed individually in metabolism cages and randomly allotted to 1 of 5 diets. A corn-based diet (97.4% corn) and 4 diets that contained both corn and each of the corn coproducts were formulated. Each diet was fed to 8 pigs. Feces and urine samples were collected using the marker to marker method with 5-d adaptation and 5-d collection periods. The DE and ME were calculated using the difference procedure. The concentrations of DE and ME in HFCG, corn bran, LCE, and CGM-LCE were less (P < 0.05) than in corn. Among corn coproducts, the concentration of DE in HFCG was greater (P < 0.05) than in corn bran, but the DE in corn bran was not different from DE values in LCE and CGM-LCE. No differences were observed in the ME concentrations among corn coproducts. In Exp. 2, 6 growing barrows (initial BW: 96.6 ± 1.16 kg) with a T-cannula in the distal ileum were randomly allotted to a 6 × 6 Latin square design with 6 diets and 6 periods. A N-free diet and 5 diets that contained corn, HFCG, corn bran, LCE, or CGM-LCE as the sole source of CP and AA were formulated. Each period lasted 7 d and ileal digesta were collected on d 6 and 7 of each period. The SID of CP and all indispensable AA was greater (P < 0.05) in corn than in all corn coproducts with the exception that the SID of Lys in corn was not different from the SID of Lys in HFCG, and the SID of Trp in corn was also not different from the SID of Trp in CGM-LCE. Among corn coproducts, the SID of CP, Arg, and Lys were greater (P < 0.05) in HFCG and CGM-LCE than in corn bran, the SID of Lys and Val was greater (P < 0.05) in LCE than in corn bran, and the SID of Arg was greater (P < 0.05) in HFCG and CGM-LCE than in LCE, but for the remaining indispensable AA, no differences among corn coproducts were observed. In conclusion, the corn coproducts used in these experiments contain less ME and have reduced SID of most AA compared with corn, but there are no differences in ME among corn coproducts and only few differences in the SID of indispensable AA among HFCG, corn bran, LCE, and CGM-LCE.

Two experiments were conducted to investigate if adjustments in diet formulations either based on total analysed amino acids or standardized ileal digestible (SID) amino acids may be used to eliminate negative effects of including heat-damaged soybean meal (SBM) or heat-damaged corn distillers dried grains with solubles (DDGS) in diets fed to weanling pigs. In Experiment 1, four corn-SBM diets were formulated. Diet 1 contained non-autoclaved SBM (315 g/kg), and this diet was formulated on the basis of analysed amino acid concentrations and using SID values from the AminoDat® 4.0 database. Diet 2 was similar to Diet 1 in terms of ingredient composition, except that the non-autoclaved SBM was replaced by autoclaved SBM at 1 : 1 (weight basis). Diet 3 was formulated using autoclaved SBM and amino acid inclusions in the diet were adjusted on the basis of analysed total amino acid concentrations in the autoclaved SBM and published SID values for non-autoclaved SBM (AminoDat® 4.0). Diet 4 also contained autoclaved SBM, but the formulation of this diet was adjusted on the basis of analysed amino acids in the autoclaved SBM and SID values that were adjusted according to the degree of heat damage in this source of SBM. Pigs (160; initial BW: 10.4 kg) were allotted to the four treatments with eight replicate pens per treatment in a randomized complete block design. Diets were fed to pigs for 21 days. The gain to feed ratio (G : F) was greater (P<0.05) for pigs fed Diet 1 compared with pigs fed the other diets and pigs fed Diet 4 had greater (P<0.05) G : F than pigs fed Diet 2. In Experiment 2, 144 pigs (initial BW: 9.9 kg) were allotted to four diets with eight replicate pens per diet. The four diets contained corn, SBM (85 g/kg) and DDGS (220 g/kg), and were formulated using the concepts described for Experiment 1, except that heat-damaged DDGS, but not heat-damaged SBM, was used in the diets. Pigs fed Diet 1 had greater (P<0.05) G : F than pigs fed Diet 2, but no differences were observed for G : F among pigs fed diets containing autoclaved DDGS. Results demonstrate that the negative effects of heat damage of SBM or DDGS may be ameliorated if the reduced concentration and digestibility of amino acids in heat-damaged SBM or DDGS is taken into account in diet formulation. Further research is needed to improve the prediction of the ileal digestibility of amino acids in heat-processed ingredients used in practical diet formulations.

An experiment was conducted to determine the influence of adding graded levels of microbial phytase to corn, distillers dried grains with solubles (DDGS), high-protein distillers dried grains (HP-DDG), and corn germ on the standardized total tract digestibility (STTD) of P. A second objective was to develop regression equations to predict the response of adding phytase to each of these ingredients. Four corn-based diets, 4 DDGS-based diets, 4 HP-DDG-based diets, and 4 corn germ-based diets were formulated. The 4 diets with each ingredient were formulated to contain 0, 500, 1,000, or 1,500 phytase units (FTU)/kg. A P-free diet was also formulated to determine basal endogenous losses of P. A total of 102 pigs (initial BW: 18.2 ± 2.1 kg) were individually housed in metabolism cages equipped with a feeder, a nipple drinker, and a screen floor that allowed for total collection of feces. Pigs were allotted to the 17 diets in a randomized complete block design with 6 replicate pigs per diet. Pigs were fed their respective diets for 12 d, and feces were collected quantitatively from d 6 to 11. Supplementation with 500, 1,000, or 1,500 FTU of microbial phytase/kg increased (linear, P < 0.01; quadratic, P < 0.05) the STTD of P in corn from 40.9 to 67.5, 64.5, and 74.9%, respectively, tended to increase (linear, P = 0.07) the STTD of P in DDGS from 76.9 to 82.9, 82.5, and 83.0%, respectively, increased (linear, P < 0.01; quadratic, P < 0.05) the STTD of P in HP-DDG from 77.1 to 88.0, 84.1, and 86.9%, respectively, and increased (linear and quadratic, P < 0.01) the STTD of P in corn germ from 40.7 to 59.0, 64.4, and 63.2%, respectively. Regression equations were developed to calculate the STTD of P in corn and corn germ, and R(2) values were 0.63 and 0.79, respectively. However, for DDGS and HP-DDG, the R(2) values were only 0.20 and 0.36, respectively, and these equations were, therefore, not considered adequate to predict the STTD of P. In conclusion, the increase in the STTD of P in corn and corn germ that is a result of microbial phytase can be predicted by regression equations, but microbial phytase has much less of an effect on the STTD of P in DDGS and HP-DDG and responses to addition of graded levels of phytase to these ingredients can, therefore, not be accurately predicted by regression equations.

The objectives of this experiment were to determine the apparent ileal digestibility and the standardized ileal digestibility (SID) of CP and AA in bakery meal, corn gluten meal, corn gluten feed, corn germ meal, and hominy feed and to compare these values with the apparent ileal digestibility and SID of CP and AA in corn and distillers dried grains with solubles (DDGS). Eight growing barrows (initial BW: 82.5 ± 5.5 kg) were randomly allotted to an 8 × 8 Latin square design with 8 diets and 8 periods. Diets contained corn, DDGS, bakery meal, corn gluten meal, corn gluten feed, corn germ meal, or hominy feed as the sole source of protein and AA. An N-free diet was used to measure basal endogenous losses of AA and protein. Pigs were fed experimental diets for eight 7-d periods, with ileal digesta being collected on d 6 and 7 of each period. Results indicated that the SID of Lys in corn gluten meal (78.7%) was greater (P < 0.01) than in DDGS, bakery meal, corn germ meal, and hominy feed (46.0, 48.4, 68.4, and 58.8%, respectively). The SID of all indispensable AA except Arg, Leu, and Met in bakery meal were not different from those in DDGS. The SID of Arg, His, Leu, and Met in corn gluten feed were less (P < 0.01) than in corn, but the SID of all other indispensable AA in corn gluten feed were not different from those in corn. However, for most indispensable AA, the SID in corn gluten feed was not different from the SID in DDGS. The SID of all indispensable AA in corn germ meal, except Arg, His, Leu, and Met, were not different from the SID in corn. Likewise, the SID of all indispensable AA in corn germ meal, except Arg and Leu, were not different from those in DDGS. The SID of Ile, Met, Phe, and Val in hominy feed were less (P < 0.01) than in corn, but the SID of the remaining indispensable AA in hominy feed were not different from the SID of indispensable AA in corn. All indispensable AA in hominy feed also had SID values that were not different from the SID values of AA in DDGS, except for Arg and Lys, which had greater (P < 0.01) SID than in DDGS. In conclusion, bakery meal had SID values of most AA that were less than in corn, but corn gluten meal had SID values for most AA that were greater than the SID of AA in corn, bakery meal, and corn coproducts.