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METABOLISM AND NUTRITION |



* Department of Animal Sciences, Purdue University, West Lafayette, IN 47907-1151;
Animal Science, Michigan State University, East Lansing, MI 48824;
Animal and Avian Sciences, University of Maryland, College Park, MD 20742; and
Evonik Degussa Corporation, Kennesaw, GA 30144
1 Corresponding author: applegt{at}purdue.edu
| ABSTRACT |
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Key Words: amino acid crude protein litter nitrogen turkey tom
| INTRODUCTION |
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Reducing dietary CP content by formulating to essential amino acid (AA) needs rather than setting a CP minimum can have considerable economic and environmental benefits. In different strains of turkeys, several researchers have noted that when essential AA requirements are met, CP recommendations of NRC (1994) are not warranted (Sell et al., 1994; Waibel et al., 1995; Boling and Firman, 1997; Kidd et al., 1997; Waldroup et al., 1997). Depending on phase feeding programs, these studies indicate that 100 to 107% of NRC (1994) recommendations for essential AA were needed to maximize growth and breast meat yield. Little if any work has been done with turkeys, however, with consideration to loss of N to the environment. Therefore, the current study was undertaken to determine if AA formulations in modern genetic strains of turkeys were warranted above NRC (1994) recommendations, and if lowering dietary crude protein by inclusion of 3 instead of 2 supplemental AA would result in measurable differences in N excretion.
| MATERIALS AND METHODS |
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Mortality was recorded twice daily, and BW of birds that died was used to adjust feed consumption and feed-to-gain ratio. At 20 wk of age, 3 birds per pen were randomly selected and euthanized with an overdose of carbon dioxide and verified by cervical dislocation. Tom BW was recorded, and the left pectoralis major was then excised and weighed.
All litter from each pen was removed within 2 d after removal of turkeys from the building. All litter from each pen was weighed and thoroughly mixed in a 256-L cement mixer (Crown Corporation Equipment, Winnepeg, Manitoba, Canada) before subsample collection. Subsamples were subsequently taken at routine intervals during the emptying of the cement mixer. Litter DM was subsequently determined in triplicate samples after drying in a forced-draft oven at 52°C for 48 h. Litter samples were then ground twice in a Wiley mill through a 1.0-mm screen. Nitrogen analyses of feed and litter were determined by the combustion method (Model FP2000, Leco Corp., St. Joseph, MI; AOAC, 2000). Diet AA content was determined according to Llames and Fontaine (1994).
All experimental data were analyzed statistically by ANOVA using the GLM procedure of SAS (SAS Institute Inc., Cary, NC) as a 2 (100 vs. 110% of NRC AA requirements) x 2 (2 vs. 3 supplemental AA) factorial experiment. Statements of significance are P
0.05 unless indicated otherwise.
| RESULTS |
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| DISCUSSION |
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In this experiment, 3 of the 4 experimental diet regimens (analyzed CP composition) were close to or above the NRC (1994) CP requirement. Results of this study, therefore, confirm previous studies by other researchers (Sell et al., 1994; Waibel et al., 1995; Boling and Firman, 1997; Kidd et al., 1997; Waldroup et al., 1997) in that feeding to meet the NRC (1994) recommendations for essential AA and lowering CP does not impact animal performance or breast meat yields. In particular, the 100% NRC formulation with 3 supplemental AA was 91.9 to 96.6% lower in analyzed dietary CP than NRC (1994) CP recommendations. Specifically, analyzed CP was 1.8, 1.8, 1.2, and 0.5 percentage units below the NRC (1994) recommendations from 4 to 8, 8 to 12, 12 to 16, and 16 to 20 wk of age, respectively. In toms reared to 18 wk of age, Kidd et al. (1997) were able to reduce dietary CP to 92% of NRC (1994) and maintain Met TSAA, Lys, Thr, and Trp at a minimum of 105% of NRC (1994) recommendations without impacting tom performance or breast meat yield. Tom performance was maintained when dietary CP was lowered to 84% of NRC (1994) recommendations and 0.1% L-Thr was supplemented to the diet, yet breast meat yields were reduced by over 6% (Kidd et al. 1997). Reductions in diet CP along with increases in supplemental AA in the current study created considerable economic savings.
Generally, as a guide, for each 1% reduction in dietary CP, estimated NH3 losses are reduced by 10% in swine and poultry (Aarnink et al., 1993; Jacob et al., 1994; Sutton et al., 1997; Kay and Lee, 1997). As animals are fed closer to true N requirements, further reductions in dietary CP may result in less pronounced reduction in N excretion and NH3 losses.
Results from this study indicate that feeding 110% NRC (1994) recommendations for AA did not result in improvements in tom performance or breast meat yield. Similarly, Moran et al. (1995) noted no improvements in performance or breast meat yields in turkeys fed 110 vs. 115% of NRC (1994) CP recommendations. In contrast, Noy and Sklan (2004) noted that toms fed 105 to 110% of NRC (1994) recommendations for AA were heavier to 9 wk of age vs. those fed 95 or 100%. Cumulative differences from 9 to 19 wk of age, however, were not apparent between treatments. Direct comparisons with the Noy and Sklan (2004) report are difficult due to differences in study phase duration (4 wk in current study vs. 3 wk) and diet energy density (up to 150 kcal/kg more in current study).
In review of experimental control diets containing corn and SBM (48% CP) from 1985 to 2002, Applegate et al. (2003) noted that average N excretion of turkey toms was 43.2% of fed N (minimum = 25%; maximum = 52.2%). Notably, most of these studies, however, were conducted with relatively young (0 to 3 wk) birds. Nevertheless in the current experiment, apparent N excretion from 0 to 20 wk of age averaged 54.9% of fed N due in part to N emission via ammonia. Wu-Haan et al. (2007) noted that in measuring emissions from poultry, 99.7% of NH3, NO, and NO2 emissions were as NH3. Therefore, the overwhelming majority of unaccounted for N likely was emitted as NH3 in this study. The correlation of N intake and pen N excretion was significant (P
0.05; data not shown), yet N intake only accounted for 29% of pen N excretion. A portion of this may be accounted for through number of dietary supplemental AA. Although not significant, the difference in apparent excretion rate due to number of supplemental AA added to the diet was nearly 2.7 percentage units lower for toms fed 3 vs. 2 supplemental AA (P
0.097). Other factors such as NH3 volatilization rate, litter moisture, litter microbial load, or a combination of factors may account for the remainder of the variation in N remaining within the litter.
In conclusion, this experiment demonstrates that diets containing AA formulations above NRC (1994) recommendations do not provide any additional performance or pectoralis major yield benefits, yet result in considerable increases in N intake (7.3%), excretion (7%), and feed cost ($0.48 per 20-wk tom). In addition, formulation with 3 supplemental AA, thereby reducing SBM inclusion, can result in a considerable reduction in N consumed (8.4%), excreted (10.8%), and feed cost ($0.37 per 20-wk tom).
| ACKNOWLEDGMENTS |
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Received for publication September 7, 2007. Accepted for publication November 24, 2007.
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