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METABOLISM AND NUTRITION |





* Faculty of Animal Science and Technology, Gansu Agricultural University, Lanzhou, China, 730070;
Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing, China, 100081;
Danisco Animal Nutrition, Marlborough, Wiltshire, SN8 1XN, United Kingdom; and
Danisco Animal Nutrition, Science Park III, Singapore, 117525
1 Corresponding author: lifd{at}gsau.edu.cn
| ABSTRACT |
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Key Words: phytase nutrient digestibility layer
| INTRODUCTION |
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The efficacy of phytase on performance and Ca and P digestibility in layers fed a corn- and soybean-based diet has been well established by Van der Klis et al. (1997), Lim et al. (2003), Panda et al. (2005), and Wu et al. (2006). However, only 2 studies have reported the effect of phytase supplementation on the digestibility of amino acids. Jalal et al. (1999) reported that supplementation of phytase in corn and soybean meal diets for layers resulted in significant improvements in the digestibility of Met, Cys, Ala, and Glu. In contrast, Snow et al. (2003) studied the effects of phytase on amino acid digestibility in molted laying hens from the age of 78 to 81 wk and found that phytase supplementation of diets based on corn, soybean meal, and meat and bone meal, with 0.25% dietary non-phytate P (NPP) and 3.55% Ca, did not affect hen performance and amino acid digestibility, although an interaction between feed type and phytase on the digestibility of amino acids was detected. Because there is limited information on the effect of phytase on the digestion and utilization of nutrients, especially energy and amino acids, the application of phytase in layer feed has not been optimized according to the diet type and phytate level in the diets. Given the diversity of feed ingredients in layer diets in the Asia-Pacific region, improvements in nutrient digestion similar to those seen in broilers are expected in layers, especially when a large proportion of by-products are included in the layer diet formulation. The current study examined the effect of phytase on feed intake, egg production, eggshell quality, and the digestion of P, Ca, energy, and amino acids in layers fed corn-, soybean-, and by-product-based diets.
| MATERIALS AND METHODS |
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The experiment included 5 dietary treatments. The positive control diet was similar to the commercial diet specifications used in China, but the nutrient specification was lower than that recommended by the NRC (1994). Negative control diets were formulated from the positive control diet, with Ca, P, and NPP levels reduced by 0.12, 0.14, and 0.13%, respectively. The other 3 diets were the negative control diet supplemented with phytase A (derived from Aspergillus niger) or phytases B and C (both derived from Escherichia coli), each at 300 phytase units/ kg of feed. The reductions of Ca and P in the negative control diet and the dose rates of phytases were recommended by the phytase suppliers and are applied by feed producers commercially. The diet formulation is listed in Table 1
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A total of 320 Hy-Line brown layers at 23 wk of age were allocated randomly into 5 treatments, with 8 replicates per treatment and 8 layers per replicate. All birds were housed in 3-layered cages and offered feed and water ad libitum. During the experimental period, birds received 16 h/d of manipulated lighting and ventilation at a natural ambient temperature of 30 to 37°C. Egg production and the health status of layers were observed as the adjustment period for 1 wk before the experiment commenced. The experimental diets were fed for 6 wk. Experimental birds were handled with care to avoid unnecessary discomfort, and all experiments were approved by the University of Gansu Agricultural University Animal Care and Use Committee. Feed intake, laying rate, and egg weight were recorded daily for each replicate. In the last week of the trial, all eggs were collected over 3 d for each replicate, and then 20 eggs from each replicate were selected randomly to measure eggshell quality. At the end of the 6-wk experiment, all diets were removed from the feeders and replaced with the respective diets containing the indigestible marker SiO2. Three days later, 6 birds in each replicate were euthanized and a section of ileum was removed by cutting from the ileocecal junction to Meckels diverticulum. A 50-mL syringe full of room-temperature deionized water was inserted into one end of the ileum and the digesta was carefully flushed out of the gut into a 10-cm-diameter Petri dish. The digesta from each replicate was pooled and freeze-dried for laboratory analysis.
Chemical Analysis
The ileal digestibility coefficients of nutrients were determined by using the inert indicator method (SiO2). The concentrations of CP and P in samples were determined according to AOAC (1990) procedures (methods 976.05 and 964.06, respectively). Indicator concentrations of samples were measured according to Van Keulen and Young (1977). The data on gross energy were determined by an oxygen bomb calorimeter (Model 1281, Parr Corp., Moline, IL), and Ca by a polarized Zeeman atomic absorption spectrophotometer (Model Z-8200, Hitachi Corp., Tokyo, Japan). Amino acids were determined by an automatic amino acid analyzer (Model S433D, Sykam Corp., Eresing, Germany) after hydrolyzing the samples in 6 M glass-distilled HCl containing 0.1% phenol for 24 h at 110°C in sealed tubes, with 2 replicates per sample. Methionine was determined in samples that had been oxidized with performic acid prior to acid hydrolysis, according to the procedure of Moore (1963), with the exception that the excess performic acid was removed by lyophilization after dilution with water.
Eggshell Quality Measurements
Eggshell hardness was measured by using a texture analyzer (Model P25, TA-XTZi Corp., Surrey, United Kingdom). The egg was laid flat on the pan of the texture analyzer and squeezed, and the shell hardness was recorded. Eggshell thickness was measured with a micrometer (Model 232, Zonechain Corp., Shanghai, China) as the average thickness of the rounded end, pointed end, and middle of the egg, excluding the inner membrane.
Statistical Analysis
Experimental data were analyzed by the ANOVA module of SPSS 10.0 software (SPSS, 1999). Significant differences were analyzed by Fishers least significant differences test at a P < 0.05 level of significance.
| RESULTS |
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| DISCUSSION |
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Supplementation of the low-Ca and low-P diet with phytases restored the performance of layers compared with the negative control diet. These results are in agreement with those of Panda et al. (2005), Lim et al. (2003), and Roland et al. (2003). Panda et al. (2005) reported that the addition of phytase to corn and soybean diets containing 0.12% NPP improved the egg production and eggshell quality of layers to the level of those fed diets containing 0.18 to 0.30% NPP. However, Rao et al. (2003) reported that adding phytase to a diet with 3.25% Ca and 0.28% NPP did not improve the performance and retention of Ca and P in the bone and serum of White Leghorn layers, suggesting that 0.28% NPP is adequate for laying hens. The comparison of egg production among phytase treatments and with the positive control group in the current study also revealed that phytase numerically improved egg production. This might have been due to the total nutrient intake, which was higher in the phytase A and B groups but not in the phytase C group compared with the positive control. In addition to the difference in feed intake, phytase can overcome the adverse effects of phytate on endogenous excretion, as shown in broilers, and can reduce the maintenance requirement of chickens fed a phytase diet (Cowieson et al., 2004), resulting in more nutrients for production.
Egg weight was not affected by phytase supplementation in the current study, a result supported by Carlos and Edwards (1998) and Jalal and Scheideler (2001). However, several published reports previously demonstrated that supplementation of phytase generally enhanced the egg production of birds, coupled with egg weight (Um and Paik, 1999; Silversides et al., 2006), which was associated with the dietary NPP level (Wu et al., 2006). We also noted that in the current study, the dietary levels of Ca and P and supplementation of phytase significantly improved eggshell thickness, but not eggshell hardness. The increase in shell thickness was not reflected in shell hardness. Although the exact reason is unknown, this result is in agreement with that reported by Um and Paik (1999), who suggested that the association between eggshell hardness and thickness was not inevitable. Shell thickness mainly depends on Ca aggregations as calcium carbonate, whereas shell hardness mainly depends on the texture, composed of Ca carbonate, organic materials, and trace minerals (Chowdhury and Smith, 2002; Mabe et al., 2003; Nakano et al., 2003).
Supplementation with phytase A, B, and C did not significantly improve the ileal digestible energy, but with the phytase C treatment the digestible energy was numerically improved by 0.49 MJ/kg. An improvement in energy by applying phytase also was reported in broilers by Ravindran et al. (2006) and Cowieson et al. (2006b). Such improvement in the energy value is a reflection of the increase in digestibility of organic nutrients, including protein, fat, and starch. However, the improvement is often small and statistical significance is difficult to reach because of the large variation among individual birds or replications and other systematic experimental error.
The supplementation of phytase significantly improved the digestion of amino acids in the current study. Theoretically, the impact of phytate on the digestion of N in birds mainly results from the phytate-protein complexes existing in feedstuffs or being formed de novo in the gastrointestinal tract under acidic conditions, consequently restricting the contact of phytase to its substrate and the digestion of refractory complexes by pepsin (Selle et al., 2000). The addition of phytase in the poultry diet partially prevents the formation of phytate-protein complexes by the prior hydrolysis of phytate, and thus increases the digestibility of protein. In the current study, adding phytase to a low-Ca and low-P corn-, soybean-, and by-product-based diet improved the ileal digestibility of amino acids by approximately 5%, with the magnitude being variable among amino acids. Ravindran et al. (2006) and Cowieson et al. (2006b) also reported that phytase could enhance the digestibility of amino acids by 1.0 to 15.7% in broilers. However, Jalal et al. (1999) and Snow et al. (2003) studied the effect of phytase on the digestibility of amino acids and found inconsistent results. Jalal et al. (1999) reported that the digestibility coefficients of Met, Cys, Ala, and Glu were significantly improved by phytase in a corn-soybean meal diet, but Snow et al. (2003) found that only the digestibility of Cys was significantly affected in a corn-, soybean-, and meat and bone meal-based diet. Importantly, in the current study phytase supplementation improved the digestibility coefficient of Met by 3%. This result is consistent with findings in broilers (Camden et al., 2001; Rutherfurd et al., 2002, 2004; Ravindran et al., 2006). Cowieson et al. (2006a) observed that phytate depressed the digestibility of sulfur amino acids more severely than the digestibility of other amino acids, suggesting that Met + Cys may be affected to a greater extent by phytate than the other amino acids.
There were no significant differences in layer performance and in the digestibility of nutrients by layers among the 3 phytase treatments in the current study. It is well understood that phytases derived from different organisms have different biochemical characteristics, such as pH profile and resistance to endogenous protease degradation, which determine their bioefficacy (Kumar et al., 2003). Increasing evidence indicates that the bacterial phytases are more effective in poultry. Augspurger et al. (2003) reported that bacterial phytase derived from E. coli liberated more P in broilers than 2 recombinant fungal phytases. Rodriguez et al. (1999) and Igbasan et al. (2000) and Kumar et al. (2003) reported that E. coli phytase was more resistant to pepsin activity than fungal phytases. Although the digestible energy data showed that phytase C (derived from E. coli) tended to be more effective than the other phytases, the results were inconclusive. More studies with diets of a lower P level are required to identify the differences in bioefficacy among these phytases.
In summary, the results of the current study demonstrated that supplementation of phytase at 300 phytase units/kg of feed in diets containing a high level of byproducts with a reduced P level restored the performance of layers to the level of a P-adequate positive control. The ileal digestibility of P, N, Ca, and amino acids was improved by phytase compared with the negative control diet, as reported in broilers. The outcomes of this study will enable layer farmers to use phytase more effectively for maximum profitability.
| ACKNOWLEDGMENTS |
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Received for publication February 15, 2007. Accepted for publication August 4, 2007.
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