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ANIMAL NUTRITION |
Department of Animal and Range Sciences, South Dakota State University, Brookings 57007
| Abstract |
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Key Words: amino acid cereal grain digestibility energy NutriDense corn pig
| INTRODUCTION |
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One such new variety is NutriDense corn, which was bred to have increased concentrations of ether extract, energy, and AA compared with yellow dent corn. To accurately establish the feeding value of NutriDense corn, it is necessary to measure the contents of DE and digestible nutrients in this ingredient and compare these values to other cereal grains.
The objectives of the current experiments were to test the hypothesis that NutriDense corn has an improved digestibility of AA compared with other cereal grains and that NutriDense corn has a greater concentration of digestible and metabolizable energy than yellow dent corn. A second objective was to determine if the concentration of AA in the test diets has an effect on the values for DE and ME that are measured.
| MATERIALS AND METHODS |
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Two experiments were conducted. In both experiments, pigs originating from the matings of SP-1 boars to Line 13 females (Ausgene Intl. Inc., Gridley, IL) were used. The cereal grains that were used were supplied by ExSeed Genetics LLC, Research Triangle Park, NC. NutriDense corn (Zea mays L.), yellow dent corn (Zea mays L.), barley (Hordeum L.), wheat (Triticum L.), and sorghum (Sorghum bicolor) were used in Exp. 1, whereas only NutriDense corn and yellow dent corn were used in Exp. 2. All grains were ground using a hammer mill with a 3-mm screen. The same batch of NutriDense corn and yellow dent corn was used in both experiments.
Experiment 1
Experiment 1 was conducted with the objective of measuring the apparent ileal digestibility (AID) and standardized ileal digestibility (SID) of CP and AA in NutriDense corn, yellow dent corn, wheat, barley, and sorghum (Table 1
). Six growing barrows (average initial BW 76.2 ± 5.6 kg) were surgically fitted with a T-cannula in the distal ileum using procedures adapted from Stein et al. (1998)
. After the surgery, the pigs were housed individually in an environmentally controlled room. Each pen (1.2 x 1.8 m) had fully slatted, metal flooring and solid concrete sidings. A feeder and a nipple drinker were installed in each pen. The room temperature was maintained at 22°C.
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The initial 5 d of each period was considered an adaptation period to the diet. During this period, 50 g of an AA mixture (Table 4
) was provided at each feeding in addition to the allotted quantity of the experimental diet. These AA were added to reduce the effects of feeding diets that did not meet the requirements of the pigs. The crystalline AA in the AA mixture were assumed to be 100% digestible and not to influence the digestibility values that were measured in the experiment.
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At the conclusion of the experiment, ileal samples were thawed, mixed within animal and diet, and a sub-sample was taken for chemical analysis. Samples of each diet and of each of the cereal grains were collected at the time of diet mixing. Digesta samples were lyophilized, and all samples were ground through a 1-mm screen before chemical analysis. All samples were analyzed for DM (procedure 4.1.06, AOAC, 2000
) and CP (Thiex et al., 2002
). All cereal grains and diets were analyzed for Ca (procedure 4.8.03, AOAC, 2000
), ADF, NDF (procedure 4.6.03, AOAC, 2000
), and ether extract (Thiex et al., 2003
). Diets and feed ingredients were digested in perchloric acid (procedure 2.3.01, AOAC, 2000
), and the concentration of P was determined on a UV-visible spectrophotometer (Model 2LV-2101 PC, Shimedzu Scientific Instruments, Colombia, MD) using a wavelength of 650 nm (procedure 3.4.11, AOAC, 2000
). The accuracy of this procedure was verified using National Institute of Standards and Technology (US Department of Commerce) reference standard 1570a (standard reference material). The GE in feed ingredients and diets were determined using bomb calorimetry (Parr Instrument 1563, Moline IL), and chromium was analyzed in diet and digesta samples according to the method of Fenton and Fenton (1979)
. Amino acid concentrations in ingredients, diets, and digesta samples were quantified on a Beckman 6300 Amino Acid Analyzer (Beckman Instruments Corp., Palo Alto, CA) using ninhydrin for postcolumn derivatization and nor-leucine as the internal standard. Samples were hydrolyzed for 24 h at 110°C with 6 N HCl before analysis. Methionine and Cys were determined as Met sulfone and cysteic acid after cold performic acid oxidation before hydrolysis. Tryptophan was determined after hydrolysis with NaOH for 22 h at 110°C.
Apparent ileal digestibilities of AA in the samples obtained from feeding the 5 cereal-containing diets were calculated. Because the cereal grain was the only feed ingredient contributing AA in each of these diets, the AID also represent the digestibilities of AA in each of the grains. Equation [1] was used for these calculations:
![]() | [1] |
where AID is the apparent ileal digestibility of an AA (%), AAd is the concentration of that AA in the ileal digesta DM, AAf is the AA concentration of that AA in the feed DM, Crf is the chromium concentration in the feed DM, and Crd is the chromium concentration in the ileal digesta DM. The AID for CP was also calculated using this equation.
The basal ileal endogenous loss (IAAend) of each AA was determined using Eq. [2], based on the flow obtained after feeding the N-free diet:
![]() | [2] |
where IAAend is the basal endogenous loss of an AA (mg per kg of DMI). The basal endogenous loss of CP was determined using the same equation.
By correcting the AID for the IAAend of each AA, standardized ileal AA digestibilities were calculated using Eq. [3]:
![]() | [3] |
where SID is the standardized ileal digestibility of an AA (%).
The values for SID were multiplied by the AA concentration (DM basis) for all cereal grains to calculate the quantities of standardized ileal digestible AA in each grain.
Data were analyzed using the MIXED procedure (SAS Inst. Inc., Cary, NC). An ANOVA was conducted, with diet as the main effect and pig and period as random effects. Means were separated using the LSMeans statement and the PDIFF option of SAS. Pig was considered the experimental unit, and an alpha value of 0.05 was used to assess differences among means.
Experiment 2
Experiment 2 was conducted with the objective of measuring the digestibility of energy and ether extract in NutriDense corn and yellow dent corn. A second objective was to compare digestibility values obtained for diets that were deficient in AA with those obtained for diets that were adequate in AA.
The NutriDense corn and the yellow dent corn used in these experiments were from the same batches as those used in Exp. 1. Two diets were formulated (Tables 5
and 6
) using NutriDense corn or yellow dent corn (99.4%) and salt, vitamins, and microminerals. Two additional diets were also formulated using NutriDense corn or yellow dent corn (97.4%), salt, vitamins, and microminerals, but crystalline AA were supplied to these diets in quantities that were needed to formulate diets that were adequate in indispensable AA (NRC, 1998
). The 2 sources of corn were the sole providers of ether extract in all diets and, with the exception of the crystalline AA, the corn sources were also the sole providers of energy in the diets.
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The quantity of feed provided per pig daily was calculated as 2.5 times the estimated requirement for maintenance energy (i.e., 106 kcal of ME per kg of BW0.75; NRC, 1998
) and was divided into 2 equal meals that were fed at 0800 and 1700. Water was available at all times. Each experimental period lasted 14 d. The initial 7 d of each period was considered an adaptation period to the diet. A marker (0.1% ferric oxide) was included in the meals that were fed in the morning of d 8 and in the morning of d 13. Fecal collections were initiated the first time after d 8 that the marker appeared in the feces and ceased the first time after d 13 that the marker appeared in the feces. All fecal samples were stored at –20°C. Urine collections were initiated on the morning of d 8 and ceased on the morning of d 13. A preservative of 6 N sulfuric acid was added to the urine collection buckets, which were covered with cheesecloth. Buckets were emptied twice daily after the total volume of urine had been recorded and a 20% subsample had been collected. The subsample was stored at –20°C.
At the conclusion of the experiment, urine samples were thawed and mixed within animal and diet, and a subsample was taken for chemical analysis. Fecal samples were dried in a forced-air oven at 60°C, finely ground, mixed, and subsampled. Fecal, urine, and feed samples were analyzed for DM, Kjeldahl N, and GE, and the diets were also analyzed for AA. Diets and fecal samples were also analyzed for ether extract. The procedures outlined for Exp. 1 were used in all analyses.
Values for DE and ME in each diet were calculated. By correcting these values for the nonenergy-containing ingredients in the diets, the energy concentrations in the feed ingredients were calculated on an as-fed and on a DM basis, as previously outlined (Stein et al., 2004
). It was assumed that the energy contributed by the crystalline AA that were included in 2 of the diets was completely digestible and that this energy was 100% retained by the pigs and did not contribute to the energy that was lost in the feces or the urine.
The retention of N (Nr) for each pig and period was calculated using Eq. [4]:
![]() | [4] |
where Nr is the retention (%) of N, Ni is the intake (g) of N from d 8 to 13, Nf is the fecal output (g) of N from d 8 to 13, and Nu is the urinary output (g) of N from d 8 to d 13.
The apparent total tract digestibility (ATTD) for energy, ether extract, and N was calculated using Eq. [5]:
![]() | [5] |
where ATTD is the apparent total tract digestibility of energy, ether extract, or N (%); Fi is the total intake of energy (kcal), ether extract (g), or N (g) from d 8 to 13; and Ff is the total fecal output of energy (kcal), ether extract (g), or N (g) originating from the feed that was fed from d 8 to 13.
Data were analyzed as a 2 x 2 factorial design, with 2 corn varieties (NutriDense and yellow dent corn) and 2 levels of crystalline AA (none or adequate), using the MIXED procedure of SAS. The interaction between corn variety and AA level was also included in the model, but the interaction was not significant for any of the variables tested and therefore was omitted in the final analysis and only main effects are presented. Means were separated using the LSMeans procedure and the PDIFF option of SAS. Pig was the experimental unit for all calculations, and an alpha level of 0.05 was used to assess significance between means.
| RESULTS |
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The AID for CP and AA in the 5 cereal grains are presented in Table 7
. The AID for CP in NutriDense corn (73.6%) was greater (P < 0.05) than in sorghum (58.8%) but not different from yellow dent corn, barley, and wheat (69.1, 70.9, and 78.5%, respectively). The AID for CP in wheat also was greater (P < 0.05) than in yellow dent corn, barley, and sorghum. For the indispensable AA, the mean AID was greater (P < 0.05) in NutriDense corn (79.3%) and wheat (79.4%) than in yellow dent corn (74.2%), barley (71.8%), and sorghum (62.3%) and was lower (P < 0.05) for sorghum than for all the other grain sources. The AID for Arg, Ile, Lys, Met, Thr, and Val also were greater (P < 0.05) in NutriDense corn than in yellow dent corn. The AID for Trp was greater (P < 0.05) in wheat compared with NutriDense corn, but for all other indispensable AA, no differences between NutriDense corn and wheat were observed. Barley had lower (P < 0.05) AID for all indispensable AA except Lys, Thr, Trp, and Val compared with NutriDense corn, but compared with yellow dent corn, only the AID for Leu was lower (P < 0.05) in barley. The AID for all indispensable AA in wheat except Lys, Trp, and Val were greater (P < 0.05) than in barley, and with the exception of Leu and Met, wheat also had greater AID for all indispensable AA compared with yellow dent corn. The AID for Thr was not different among sorghum, yellow dent corn, and barley, but for all other indispensable AA, sorghum had values for AID that were lower (P < 0.05) than in the other cereal grains.
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The SID for CP was lower (P < 0.05) in sorghum compared with the other grains, but there was no difference among NutriDense corn, yellow dent corn, and wheat (Table 8
). The SID for Arg, Lys, and Met were greater (P < 0.05) in NutriDense corn compared with yellow dent corn, but for the remaining indispensable AA and for the mean of all indispensable AA, no differences in SID between the 2 corns were observed. The SID for Trp in NutriDense corn was lower (P < 0.05) than in wheat, but for all other indispensable AA and for the mean of the indispensable AA, no differences in SID between NutriDense corn and wheat were observed. The SID for Ile, Lys, and Trp were not different in NutriDense corn and barley, but for all other indispensable AA and for the mean of all indispensable AA, the SID in NutriDense corn were greater (P < 0.05) than in barley. The SID for all indispensable AA except Lys and Trp and the mean of all indispensable AA in barley were lower (P < 0.05) than in wheat, but with the exception of Leu and Met, there were no differences in SID between barley and yellow dent corn. The SID for all indispensable AA except Ile and Trp and the SID for the mean of all indispensable AA also were similar in yellow dent corn and wheat. For sorghum, the SID for all indispensable AA and the mean of all indispensable AA were lower (P < 0.05) than in the other cereal grains.
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The concentrations of standardized ileal digestible CP and all indispensable AA were greater (P < 0.05) in NutriDense corn than in yellow dent corn and with the exception of Ile, Leu, Phe, and Val, these concentrations were greater (P < 0.05) than in sorghum (Table 9
). However, with the exception of Leu and Met, greater (P < 0.05) concentrations of standardized ileal digestible CP and indispensable AA were present in wheat and barley than in NutriDense corn. For the dispensable AA, NutriDense corn had greater concentrations of standardized ileal digestible Ala, Cys, Glu, and Tyr than yellow dent corn (P < 0.05), but with the exception of Ala and Cys, the standardized ileal digestible concentration of all dispensable AA was lower (P < 0.05) in NutriDense corn than in barley and wheat.
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The DE (3,423 kcal/kg) and ME (3,355 kcal/kg) in the diets containing NutriDense corn were greater (P < 0.05) than the DE (3,338 kcal/kg) and the ME (3,270 kcal/kg) in the diets containing yellow dent corn. As a consequence, the DE and ME in NutriDense corn (4,004 and 3,922 kcal/kg of DM, respectively) were greater (P < 0.01) than the DE and ME in yellow dent corn (3,878 and 3,799 kcal/kg of DM, respectively). The addition of crystalline AA to the diets did not influence the DE and ME values in the 2 sources of corn.
The absorption and retention of N and the biological value of the protein were not influenced by the source of corn. However, the addition of crystalline AA increased (P < 0.01) N absorption, N retention, and the biological value of protein in the diets.
The ATTD for N was not affected by the source of corn (Table 11
), but was greater (P < 0.01) for diets that contained crystalline AA (82.6%) than for diets without crystalline AA (77.3%). The ATTD of ether extract in NutriDense corn was greater (P < 0.01) than in yellow dent corn (61.4 vs. 46.2%), but there were no effects of AA supplementation on the ATTD of ether extract. For energy, no effect of grain source on ATTD was observed, but the addition of AA to the diets increased (P < 0.05) ATTD (87.6 vs. 86.3%).
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| DISCUSSION |
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Energy and Nitrogen Balance and Digestibility
The values for DE and ME in yellow dent corn (3,878 and 3,799 kcal/kg of DM) concur with the values of 3,879 kcal of DE and 3,825 kcal of ME per kg of DM reported by Stein et al. (2004)
. Likewise, the values obtained in the current experiment agree with the values of 3,961 kcal of DE and 3,843 kcal of ME per kg of DM published by NRC (1998)
. The greater concentration of GE in NutriDense corn as compared with yellow dent corn was likely caused by the increased concentration of ether extract in this grain. The ATTD for GE was not different between the 2 corns. The difference in GE concentration, therefore, resulted in differences in the concentration of DE and ME between the 2 corns with NutriDense corn containing more DE and ME per kilogram than yellow dent corn. This demonstrates that pigs are able to utilize the increased concentration of energy in NutriDense corn. This observation is in agreement with data indicating that the G:F for growing pigs is improved if NutriDense corn rather than yellow dent corn is included in the diets (Hastad et al., 2005
).
The increased ATTD for ether extract in NutriDense corn as compared with yellow dent corn is most likely a result of the greater concentration of ether extract in NutriDense corn. The endogenous losses of ether extract will contribute relatively more to the total fecal output in diets with low concentrations of ether extract compared with diets with higher concentrations of ether extract. This in turn will lead to a lower calculated value for ATTD in diets with a low concentration of ether extract (Just et al., 1980
; Just, 1982
). To determine if the ether extract in NutriDense corn per se is more digestible than in yellow dent corn, it will be necessary to measure the true rather than the apparent digestibility of ether extract in the 2 varieties of corns.
The direct procedure was used to measure the DE and ME in the 2 corns in the present experiment. This procedure has previously been used to estimate DE and ME in corn (Adeola and Bajjalieh, 1997
; Stein et al., 2004
). By necessity, experimental diets that are deficient in AA are formulated when this approach is used. In the current experiment, an attempt was made to correct this deficiency by supplementing the experimental diets with crystalline AA. Based on the ADG for the pigs, the data for the N balance, the ATTD for N, and the biological value of the diets, it is clear that diets were more balanced in AA when formulated using this approach. As expected, the diets containing crystalline AA resulted in more protein being retained and, therefore, less excretion of N in the urine. The improved protein balance also resulted in more energy being absorbed from the diets as indicated by a greater ATTD for GE in the AA-supplemented diets compared with the unsupplemented diets. However, the lack of an effect of crystalline AA on values for DE and ME in the 2 grains indicates that the accuracy of measuring DE and ME is not improved by balancing diets with AA.
In conclusion, results from the current research demonstrate that NutriDense corn has a greater concentration of standardized ileal digestible AA and of ether extract compared with yellow dent corn. As a consequence, if NutriDense corn is used in diet formulations rather than yellow dent corn, less supplemental protein is needed to balance the diet. NutriDense corn also contains more digestible and metabolizable energy than yellow dent corn, which is expected to improve feed conversion if NutriDense corn is used. However, wheat and barley contain greater quantities of digestible AA than NutriDense corn and yellow dent corn, whereas the concentration of digestible AA in sorghum is less than in all other cereal grains. Therefore, if diets are formulated based on barley or wheat, lower concentrations of supplemental protein sources are needed than if NutriDense corn, yellow dent corn, or sorghum is used.
| Footnotes |
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2 NutriDense corn is a registered trade name by ExSeed Genetics LLC, Research Triangle Park, NC. ![]()
3 Financial support from ExSeed Genetics LLC, Research Triangle Park, NC, is greatly appreciated. ![]()
4 Current address: Danisco Animal Nutrition, Marlborough, Wiltshire, UK. ![]()
5 Current address: Pipestone County Extension Office, Pipestone, MN. ![]()
6 Current address: University of Illinois, Department of Animal Sciences, West Gregory Dr., Urbana 61801. ![]()
7 Corresponding author: hstein{at}uiuc.edu
Received for publication September 10, 2006. Accepted for publication April 4, 2007.
| LITERATURE CITED |
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