Evaluation of Phytase Enzyme with Chicks Fed Basal Diets Containing Different Soybean Meal Samples

Soybean meal contains approximately 0.62% total P of which 0.4% can be phytate P, which is considered less biologically available for poultry than other forms of P. Soybean meal is a key ingredient in poultry feeds and information is needed about the range of phytate P and nonphytate P in different soybean meals. The phytate P content of soybeans may vary due to climatic conditions, soil type and soybean variety. Previous research has shown that phytate P can be hydrolyzed in the gastrointestinal tract providing available P by adding a commercial phytase enzyme to poultry feed. The extent of phytate hydrolysis by dietary supplementation of phytase has been shown to vary depending on the type of dietary ingredients such as corn, soybean meal, canola meal, and wheat. Research is needed to determine if different commercially available soybean meals respond in a similar manner to a feed added phytase. Twenty-five soybean meal samples were collected from active soybean crushing plants in the United States and 18 of the samples were selected to evaluate the effect of a microbial phytase on phytate P disappearance using 5-d bioassays. The range of analyzed values in soybean meal samples for total P, phytate P, Ca, protein, and neutral detergent fiber (NDF) were 0.59 to 0.87, 0.32 to 0.42, 0.28 to 0.54, 40.44 to 51.69, and 7.78 to 16.09%, respectively. Bioassay results indicate that body weight, feed consumption, and feed conversion ratio improved significantly (P < 0.05) in some of the groups fed diets with enzyme compared with groups fed the same diet with no added enzyme. The range of total P retention and phytate P disappearance for groups fed diets with no enzyme were 21.35 to 48.41 and 13.64 to 37.13%, respectively. The addition of phytase increased total P retention and phytate P disappearance from 56.81 to 68.62 and 76.18 to 94.08%, respectively. The results indicate no correlation among components (total P, phytate P, Ca, protein, and NDF) of soybean meal samples, percentage of phytate P disappearance, and percentage of total P retention for groups fed diets with and without added phytase.     

Relationship between mineral availabilities and dietary phytate in animals

A large amount of phosphorus (P) in corn and soybean meal is in the form of phytate that is poorly available to monogastric animals. It leads to the presence of large amounts of P in manure, which contributes to the P pollution problem. The fermentation of soybean meal with Aspergillus usamii almost completely degraded phytate and improved P availability in chicks. Although dietary yeast phytase increased P absorption and availability in pigs, its efficacy was less than that of Aspergillus niger phytase. It was suggested that the lesser efficacy of yeast phytase resulted from its lower stability against pepsin. Phytate suppresses zinc availability in monogastric animals. Zinc availability was improved by the substitution of regular soybean meal with fermented soybean meal and by the supplementation with Aspergillus niger phytase in pigs. It has been considered that phytate is easily degraded in the rumen and the availability of phytate P is high in ruminants. However, 20% of phytate in oilseed meals was not degraded in the rumen of sheep. Additionally, heating and formaldehyde treatments with oilseed meals suppressed ruminal degradation of phytate and approximately half of phytate escaped from ruminal degradation in the treated oilseed meals.     

Consequences of calcium interactions with phytate and phytase for poultry and pigs

Despite increasing practical experience and cascades of scientific reports on exogenous microbial phytases, several issues associated with their use remain unresolved because of the ambiguous and, at times, conflicting data that has been generated. One possible cause of these inconsistent outcomes is dietary calcium (Ca) levels, which are mainly derived from limestone. Thus the purpose of this review is to examine Ca interactions with dietary phytate and phytases, particularly exogenous, microbial phytases, and their consequences for poultry and pigs. The polyanionic phytate molecule has a tremendous capacity to chelate cations and form insoluble Ca–phytate complexes, which are refractory to phytase activity. Thus Ca–phytate complex formation along the gastrointestinal tract, where one phytate (IP₆) molecule binds up to five Ca atoms, assumes importance and approximately one third of dietary Ca may be bound to phytate in digesta. Consequently, phytate limits the availability of both P and Ca as a result of insoluble Ca–phytate complex formation, the extent of which is driven by gut pH and molar ratios of the two components. It is accepted that Ca–phytate complexes are mainly formed in the small intestine where they have a substantial negative influence on the efficacy of mucosal phytase. However, exogenous phytases are mainly active in more proximal segments of the gut and lower pH levels, so their efficacy should not be influenced by Ca–phytate complexes in the small intestine. There is, however, data to indicate that Ca and phytate interactions occur under acidic conditions with the formation of soluble and insoluble Ca–phytate species, which could negatively impact on exogenous phytase efficacy. Also, Ca will tend to elevate gut pH because of limestone's very high acid binding capacity, which will favour Ca–phytate interactions and may influence the activity of exogenous phytases depending on their pH activity spectrum. The de novo formation of binary protein–phytate complexes that are refractory to pepsin hydrolysis may be fundamental to the negative impact of phytate on the digestibility of protein/amino acids. However, high dietary Ca levels may disrupt protein–phytate complex formation by interacting with both phytate and protein even at acidic pH levels, thereby influencing the outcomes of phytase amino acid digestibility assays. Finally, it is increasingly necessary to define the Ca and nonphytate-P requirements of pigs and poultry offered phytase-supplemented diets.     

Brewer's yeast efficiently degrades phytate phosphorus in a corn-soybean meal diet during soaking treatment

Microbes such as yeast and Aspergillus are known to produce phytase, and Aspergillus phytase has been used as a feed additive for improving phytate-phosphorus bioavailability in monogastric animals. We measured phytase activity in some by-products from fermented food and beverage productions by yeast and Aspergillus . The phytase activity was as high as 3577 and 2225 PU/kg DM in raw and dried brewer's yeasts, respectively. On the other hand, the phytase activity was approximately 400 PU/kg DM in white-wine yeast and red-wine yeast. The phytase activity was further low in natto (fermented soybean) residue, soy sauce cake, rice brewer's grain and the activity was not detected in dried corn-barley distiller's grain with soluble and sweet-potato distiller's residue. The stability of phytase against pepsin was much lower in the brewer's yeast than in an Aspergillus phytase preparation. On the other hand, the addition of raw brewer's yeast effectively degraded phytate phosphorus in a corn-soybean meal diet during soaking. These results suggest that phytase in the examined by-products is not suitable for the phytase source of conventional diets, but that the soaking treatment with a raw brewer's yeast is an alternative method for improving phytate-phosphorus bioavailability in corn-soybean meal diets for pigs.     

Comparative enzymatic hydrolysis of phytate in various animal feedstuff with two different phytases

Bacillus amyloliquefaciens DS11 phytase (DS11 phytase) and Aspergillus ficuum phytase (AF phytase) activities were investigated by measuring the release of phosphate from phytate in animal feedstuff such as wheat bran, corn meal, soybean meal and rice flour at pH 5 and 7. In all the tested feedstuff, the enzymatic activity of DS11 phytase was more active at pH 7, but that of AF phytase was more active at pH 5. From these results, the phytate in the gastrointestinal tract could be degraded in the small intestine or stomach by DS11 or AF phytase, respectively. In conclusion, the results presented in this paper indicated that different combination ratios of DS11 and AF phytase, depending on the kind of feedstuff, might effectively induce more enzymatic activity both in the stomach and small intestine in terms of the pH of the gastrointestinal tract.     

The effect of microbial phytase on ileal phosphorus and amino acid digestibility in the broiler chicken

1. The study aimed to assess the effect of a commercially available microbial phytase on phytate phosphorus and total phosphorus content at the terminal ileum as well as true ileal amino acid digestibility. 2. Five diets, each containing a different plant-based feedstuff, were supplemented with microbial phytase and fed, along with a non-supplemented corresponding diet, to 28-d-old broiler chickens, Chromic oxide was used as an indigestible marker. Ileal contents were collected and analysed, along with the diets, for total phosphorus, phytate phosphorus and amino acids. 3. Endogenous phosphorus determined at the terminal ileum was 272 +/- 108 mg/kg food dry matter (mean +/- SE). Endogenous ileal amino acid flows ranged from 58 +/- 10 mg/kg food dry matter for methionine to 568 +/- 47 mg/kg food dry matter for glutamic acid. 4. Supplementation with microbial phytase resulted in a significantly greater phytate P disappearance from the terminal ileum for rice bran (17% units), but not for soyabean meal, maize, wheat or rapeseed meal. Similarly total phosphorus digestibility was significantly (P < 0.05) higher when microbial phytase was added to the rice-bran-based diet but not for any of the other feedstuffs. 5. Amino acid digestibility was significantly greater in the presence of microbial phytase for all the amino acids examined in wheat, for several of the amino acids each in maize and rapeseed meal and for one amino acid in rice bran and soyabean meal. The average increase in amino acid digestibility for those amino acids affected, was 13, 6, 10, 7 and 12% units for wheat, maize, rapeseed meal, rice bran and soyabean meal, respectively. 6. It appears that microbial phytase improves phosphorus digestibility and amino acid digestibility for certain plant-based feedstuffs.     

Ileal digestibility of amino acids,phosphorus, phytate and energy in pigs fed sorghum‐based diets supplemented with phytase and Pancreatin®

The effects of phytase supplementation on the apparent ileal digestibility (AID) of amino acids (AA) have been inconsistent. Two experiments evaluated the effect of providing a mixture of pancreatic enzymes (Pancreatin^®) to growing pigs fed sorghum–soybean meal diets supplemented with phytase on the AID of AA, energy, and phosphorus (P), as well as the ileal digestibility (ID) of phytate; there were four periods per experiment. In Experiment 1, eight pigs (BW 22.1 ± 1.3 kg) were fitted with a T‐cannula at the distal ileum. Each period consisted of 9 days; 7 days for diet adaptation, and 2 days for digesta collection. Treatments (T) were: (i) basal sorghum–soybean meal diet, (ii) basal diet plus Pancreatin^®, (iii) basal diet plus phytase and (iv) basal diet plus phytase and Pancreatin^®. Phytase increased the digestibilities of phytate and P (p < 0.001), but did not affect the AID of AA and energy (p > 0.10). Except for methionine (p = 0.07), Pancreatin^® did not affect the AID of AA. Phytase and Pancreatin^® did not interact (p > 0.10). Experiment 2 was similar to Experiment 1, but Pancreatin^® was infused into duodenum. Pancreatin^® infusion did not affect the AID of AA (p > 0.10); and tended to reduce (p = 0.09) the AID of lysine. Phytase × Pancreatin^® interactions were not observed (p > 0.10). In conclusion, phytase and Pancreatin^® did not improve the AID of AA in growing pigs fed sorghum–soybean meal diets indicating that phytates did not affect AA digestibility.     

Total and water-soluble phosphorus excretion from swine fed low-phytate soybeans

A study was conducted to evaluate the impact of feeding soybean meal (SBM) from low-phytate (LP) or traditional phytate (TP) soybeans on performance and excretions from growing swine. Ninety-six crossbred barrows (initial BW = 18 +/- 0.3 kg) were allocated by BW to 24 pens and fed 1 of 4 treatment diets: TP SBM without supplemental phytase; TP SBM plus 500 phytase units of phytase/kg, as-fed basis [Ronozyme P (CT) 2500; DSM Nutritional Products, Basel, Switzerland]; LP SBM (USDA-ARS breeding line CX1834-1) without supplemental phytase, and LP SBM plus phytase. All diets within a feeding phase were formulated to be isocaloric and have similar available Lys and nonphytin P content. Pens were assigned randomly to treatments at the beginning of each of the 4 feeding phases. An indigestible marker was added to the mash feed. Individual pig weights and fecal samples were collected, and feed disappearance by pen was recorded weekly. No phytase inclusion or SBM source effects were observed for pen ADG, ADFI, or G:F (P > 0.05). Total tract apparent digestibility of DM and OM was not different among treatment groups (P > 0.05). Apparent digestibility of P was greater for pigs fed diets containing the LP SBM (48.9 vs. 42.4%; P < 0.01) and less when diets included phytase (44.3 vs. 47.0%; P < 0.0001). Total P (tP) and water-soluble P (WSP) excreted were affected by dietary treatment (tP: 20.0, 18.0, 16.8, and 13.8 g/kg of feces DM, P < 0.01; and WSP: 10.9, 10.1, 9.1, and 8.5 g/kg, P < 0.01, for TP SBM without supplemental phytase, TP SBM plus 500 phytase units of phytase/kg, LP SBM without supplemental phytase, and LP SBM plus phytase diets, respectively). Inclusion of phytase decreased tP and WSP excreted (P < 0.01), as did use of LP SBM (P < 0.01). Diet effects on the fraction of excreted tP that was WSP were observed (P < 0.01); however, there was not a significant effect of SBM source. Inclusion of exogenous phytase in diets increased the proportion of tP that was excreted as WSP from 55% in diets without phytase to 59% in diets containing phytase. The findings suggest that there is a need for LP soybeans as a dietary component to minimize environmental impacts.     

The presence of inositol phosphates in gastric pig digesta is affected by time after feeding a nonfermented or fermented liquid wheat- and barley-based diet

The objective was to quantify the retention of digesta and evaluate the degradation of phytate or inositol hexakisphosphate (InsP(6)) and lower inositol phosphates (InsP?, InsP?, InsP?, and InsP?) in the stomach at different times after feeding pigs a fermented liquid diet with microbial phytase or a nonfermented diet with or without microbial phytase. Six barrows fitted with gastric cannulas were used. The experiment was a 3 × 3 Latin square with 3 pigs fed 3 diets during 3 wk in 2 replicates. Each experimental period lasted for 7 d, comprising 3 d of adaptation and 4 d of total collection of gastric digesta. For each pig, the digesta was collected once daily at 1, 2, 3, or 5 h after feeding the morning meal. A basal wheat- and barley-based diet was steam-pelleted at 90°C. The dietary treatments were a nonfermented basal diet (NF-BD), the NF-BD with microbial phytase (750 phytase units of phytase/kg, as-fed basis; NF-BD + phytase), and the NF-BD + phytase fermented for 17.5 h (F-BD + phytase). Gastric InsP?-P was not detected at all in pigs fed F-BD + phytase because of complete InsP? degradation during fermentation of the feed before feeding. Gastric InsP?-P decreased over time (P < 0.05) in pigs fed NF-BD and NF-BD + phytase. The decreases were 45, 54, 56, and 61 percentage points greater at 1, 2, 3, and 5 h, respectively, in pigs fed NF-BD + phytase compared with NF-BD. However, substantial amounts of InsP? still passed into the small intestine in pigs fed NF-BD + phytase, especially within the first hour (estimated to 17% of InsP?-P intake). The accumulation of lower inositol phosphates in gastric digesta was very small for all treatments and at all times because of a rapid and almost complete degradation. In conclusion, phytase addition to the nonfermented diet increased the degradation of gastric InsP?. However, considerable amounts of intact InsP? still passed into the small intestine because of a shortage of time for InsP? degradation in the stomach. Therefore, to increase the apparent digestibility of plant P in dry wheat- and barley-based diets, the development of phytases that can degrade InsP? effectively immediately after ingestion of the feed at an initial gastric pH from 6.5 to 5.0 is needed. Feeding F-BD + phytase compensated for the shortage of time because the InsP? degradation was completed during fermentation before feeding. The degradation of InsP? to InsP? is the bottleneck for plant P utilization in pigs because the degradation of the lower inositol phosphates is rapid and almost complete.     

Phytate in pig and poultry nutrition

Phosphorus (P) is primarily stored in the form of phytates in plant seeds, thus being poorly available for monogastric livestock, such as pigs and poultry. As phytate is a polyanionic molecule, it has the capacity to chelate positively charged cations, especially calcium, iron and zinc. Furthermore, it probably compromises the utilization of other dietary nutrients, including protein, starch and lipids. Reduced efficiency of utilization implies both higher levels of supplementation and increased discharge of the undigested nutrients to the environment. The enzyme phytase catalyses the stepwise hydrolysis of phytate. In respect to livestock nutrition, there are four possible sources of this enzyme available for the animals: endogenous mucosal phytase, gut microfloral phytase, plant phytase and exogenous microbial phytase. As the endogenous mucosal phytase in monogastric organisms appears incapable of hydrolysing sufficient amounts of phytate‐bound P, supplementation of exogenous microbial phytase in diets is a common method to increase mineral and nutrient absorption. Plant phytase activity varies greatly among species of plants, resulting in differing gastrointestinal phytate hydrolysis in monogastric animals. Besides the supplementation of microbial phytase, processing techniques are alternative approaches to reduce phytate contents. Thus, techniques such as germination, soaking and fermentation enable activation of naturally occurring plant phytase among others. However, further research is needed to tap the potential of these technologies. The main focus herein is to review the available literature on the role of phytate in pig and poultry nutrition, its degradation throughout the gut and opportunities to enhance the utilization of P as well as other minerals and nutrients which might be complexed by phytates.     

Phytase dose effects in practically formulated diets that vary in ingredient composition on feed manufacturing and broiler performance

Considering approaches to efficiently produce broiler chickens, an experiment was conducted to describe the manufacturing and feeding effects of a corn, soybean meal, and wheat based diet with varying levels of corn distillers dried grains with solubles (DDGS) and commercial phytase. Treatments were arranged in a 3 × 2 factorial randomized complete block design varying in phytase (zero, 1,000, and 6,000 FTU/kg) and DDGS inclusion (zero or 5%). Phytase inclusion decreased dietary non-phytate phosphorous (nPP) and total Calcium (Ca) in formulation by 0.12 and 0.1%, respectively. Diets were steam conditioned at 82°C for 10 s, extruded through a 4.7 × 38 mm pellet die, and fed as crumbles (starter and grower) or pellets (finisher). Ten replicate pens of straight-run Hubbard × Cobb 500 chicks consumed one of 6 dietary treatments for 38 days. Phytase improved feed conversion ratio (FCR) in the starter period (P = 0.05), but benefits were not apparent in the grower or finisher periods. Phytase and formulation main effects interacted to affect overall FCR (P = 0.05), demonstrating a 0.05 decrease in FCR when birds were fed a diet containing a super-dose of phytase and without DDGS relative to diets containing a super-dose of phytase and DDGS. The DDGS likely provided reduced nutrient availability relative to their nutrient values used for diet formulation or provided non-starch polysaccharides (NSP) at a level that decreased bird performance. Based on tibia ash measures, performance improvement associated with the super-dose of phytase was likely associated with reducing phytate phosphorus gastrointestinal irritation rather than meeting bird phosphorus requirement.     

Utilization of distillers dried grains with solubles and phytase in sow lactation diets to meet the phosphorus requirement of the sow and reduce fecal phosphorus concentration

Two experiments were completed to determine the potential for using distillers dried grains with solubles (DDGS) in diets with or without phytase to provide available P, energy, and protein to highly productive lactating sows without increasing their fecal P. In Exp. 1, the dietary treatments were as follows: (1) corn and soybean meal with 5% beet pulp (BP) or (2) corn and soybean meal with 15% DDGS (DDGS). Besides containing similar amounts of fiber, diets were isonitrogenous (21% CP, 1.2% Lys) and isophosphorus (0.8% P). Sixty-one sows were allotted to dietary treatments at approximately 110 d of gestation (when they were placed in farrowing crates) based on genetics, parity, and date of farrowing. Sows were gradually transitioned to their lactation diet. On d 2 of lactation, litters were cross-fostered to achieve 11 pigs/litter. Sows and litters were weighed on d 2 and 18. Fecal grab samples were collected on d 7, 14, and 18 of lactation. Dietary treatment did not affect the number of pigs weaned (10.9 vs. 10.8) or litter weaning weight. On d 14, DDGS sows had less fecal P concentration than BP sows (28.3 vs. 32.8 mg/g; P = 0.04). Fecal Ca of sows fed DDGS decreased for d 7, 14, and 18 (55.6, 51.4, and 47.1 mg/g of DM, respectively; P = 0.05) but not for BP sows. In Exp. 2, the dietary treatments were as follows: (1) corn and soybean meal (CON), (2) CON + 500 phytase units of Natuphos/kg diet, as fed (CON + PHY), (3) corn and soybean meal with 15% DDGS and no phytase (DDGS), or (4) DDGS + 500 FTU of Natuphos/kg of diet, as fed (DDGS + PHY). Sows (n = 87) were managed as described for Exp 1. Litter BW gain (46.0, 46.3, 42.1, and 42.2 kg; P = 0.25) and sow BW loss (8.1, 7.2, 7.4, and 6.3 kg for CON, CON + PHY, DDGS, and DDGS + PHY, respectively; P = 0.97) were not affected by dietary treatment. Fecal P concentration did not differ among dietary treatments but was reduced at d 14 and 18 compared with d 7 (P = 0.001). However, fecal phytate P concentration was decreased by the addition of DDGS when DDGS and DDGS + PHY were compared with the CON sows except on d 7 (P < 0.05). Sows fed CON diet had greater fecal phytate P than sows fed DDGS, and sows fed DDGS + PHY had less fecal phytate P than sows fed DDGS with no phytase (P = 0.001). Although these experiments were only carried out for 1 lactation, these results indicate that highly productive sows can sustain lactation performance with reduced fecal phytate P when fed DDGS and phytase in lactation diets.     

Phytase improves iron bioavailability for hemoglobin synthesis in young pigs.

Dietary phytase supplementation improves bioavailabilities of phytate-bound minerals such as P, Ca, and Zn to pigs, but its effect on Fe utilization is not clear. The efficacy of phytase in releasing phytate-bound Fe and P from soybean meal in vitro and in improving dietary Fe bioavailability for hemoglobin repletion in young, anemic pigs was examined. In Exp. 1, soybean meal was incubated at 37 degrees C for 4 h with either 0, 400, 800, or 1,200 units (U) of phytase/kg, and the released Fe and P concentrations were determined. In Exp. 2, 12 anemic, 21-d-old pigs were fed either a strict vegetarian, high-phytate (1.34%) basal diet alone, or the diet supplemented with 50 mg Fe/kg diet (ferrous sulfate) or phytase at 1,200 U/kg diet (Natuphos, BASF, Mt. Olive, NJ) for 4 wk. In Exp. 3, 20 anemic, 28-d-old pigs were fed either a basal diet with a moderately high phytate concentration (1.18%) and some animal protein or the diet supplemented with 70 mg Fe/kg diet, or with one of two types of phytase (Natuphos or a new phytase developed in our laboratory, 1,200 U/kg diet) for 5 wk. In Exp. 2 and 3, diets supplemented with phytase contained no inorganic P. In Exp. 1, free P concentrations in the supernatant increased in a phytase dose-dependent fashion (P<.05), whereas free Fe concentrations only increased at the dose of 1,200 U/kg (P<.10). In Exp. 2 and 3, dietary phytase increased hemoglobin concentrations and packed cell volumes over the unsupplemented group; these two measures, including growth performance, were not significantly different than those obtained with dietary supplemental Fe. In conclusion, both sources of phytase effectively degraded phytate in corn-soy diets and subsequently released phytate-bound Fe from the diets for hemoglobin repletion in young, anemic pigs.     

Influence of a novel consensus bacterial 6-phytase variant on mineral digestibility and bone ash in young growing pigs fed diets with different concentrations of phytate-bound phosphorus

A 20-d experiment was conducted to test the hypothesis that phytase increases nutrient digestibility, bone ash, and growth performance of pigs fed diets containing 0.23%, 0.29%, or 0.35% phytate-bound P. Within each level of phytate, five diets were formulated to contain 0, 500, 1,000, 2,000, or 4,000 phytase units (FTU)/kg of a novel phytase (PhyG). Three reference diets were formulated by adding a commercial Buttiauxella phytase (PhyB) at 1,000 FTU/kg to diets containing 0.23%, 0.29%, or 0.35% phytate-bound P. A randomized complete block design with 144 individually housed pigs (12.70 ± 4.01 kg), 18 diets, and 8 replicate pigs per diet was used. Pigs were adapted to diets for 15 d followed by 4 d of fecal collection. Femurs were collected on the last day of the experiment. Results indicated that diets containing 0.35% phytate-bound P had reduced (P < 0.01) digestibility of Ca, P, Mg, and K compared with diets containing less phytate-bound P. Due to increased concentration of total P in diets with high phytate, apparent total tract digestible P and bone ash were increased by PhyG to a greater extent in diets with 0.29% or 0.35% phytate-bound P than in diets with 0.23% phytate-bound P (interaction, P < 0.05). At 1,000 FTU/kg, PhyG increased P digestibility and bone P more (P < 0.05) than PhyB. The PhyG increased (P < 0.01) pig growth performance, and pigs fed diets containing 0.35% or 0.29% phytate-bound P performed better (P < 0.01) than pigs fed the 0.23% phytate-bound P diets. In conclusion, the novel phytase (i.e., PhyG) is effective in increasing bone ash, mineral digestibility, and growth performance of pigs regardless of dietary phytate level.     

Effects of level of supplemental phytase on ileal digestibility of amino acids, calcium, and phosphorus in dehulled soybean meal for growing pigs.

Ileally cannulated pigs were used to assess the effects of four dietary levels of microbial phytase (Natuphos) on the apparent and true digestibility of Ca, P, CP, and AA in dehulled soybean meal. Fourteen pigs (25 kg initial BW) were surgically fitted with T-cannulas at the terminal ileum and assigned to diets in a replicated 7 x 7 Latin square design. Following a 14-d recovery, four diets consisting of 30.5% soybean meal with 0, 500, 1,000, or 1,500 units of phytase/kg of diet were fed. Diets 5 (1.05% lysine, 0.90% Ca, and 0.75% P) and 6 (1.05% lysine, 0.90% Ca, and 0.75% P) contained 35.25% soybean meal and 27.0% soy protein concentrate, respectively. Diet 7 (0.37% lysine, 0.03% Ca, and 0.05% P) was a low-CP, casein-based diet used to estimate the nonspecific endogenous losses of Ca, P, CP, and AA in order to estimate the true digestibility of these nutrients. All diets contained cornstarch and dextrose and were fortified with vitamins and minerals. Chromic oxide was used as an indigestible indicator. The diets were fed daily at 9% of metabolic BW (BW0.75). Apparent and true ileal digestibility of P increased quadratically (P < 0.01) and true digestibility of Ca increased linearly (P < 0.07) with increasing levels of phytase. Apparent digestibility of Ca was unaffected (P = 0.15) by phytase level. Apparent and true ileal digestibility of CP and most AA increased slightly with the addition of 500 units of phytase/kg of diet, but not at higher levels of phytase supplementation (in most cases, cubic effect, P < 0.05). Apparent and true ileal nutrient digestibility coefficients were unaffected by soybean meal source (Diet 1 vs Diet 5), except for arginine and Ca. The apparent and true digestibility coefficients for most of the AA tended (P < 0.10) to be lower in diets containing soy protein concentrate vs the common source of soybean meal used in Diet 5, but ileal digestibilities of Ca and P were unaffected (P = 0.15). In this study, supplemental microbial phytase did not improve the utilization of AA provided by soybean meal but was an effective means of improving Ca and P utilization by growing swine fed soybean meal-based diets.     

Influence of phytate level on broiler performance and the efficacy of 2 microbial phytases from 0 to 21 days of age

Phytate is an antinutrient in animal feeds, reducing the availability and increasing the excretion of nutrients. Phytases are widely used to mitigate the negative influences of phytate. This trial was designed to compare the efficacy of 2 Escherichia coli-derived phytases on broiler performance and bone ash as influenced by dietary phytate level. A total of 1,024 Arbor Acres male broilers were used with 8 replicate pens of 16 birds/pen. Experimental diets were based on low available phosphorus (avP; 1.8 g/kg) with low (6.40 g/kg) or high (10.65 g/kg) phytate. The low-avP diets were then supplemented with mono-dicalcium phosphate to increase the avP level to 4.5 g/kg, 500 phytase units/kg of phytase A, or 500 phytase units/kg of phytase B to create 8 experimental diets. Feed intake, BW gain, FCR, and livability were influenced by a P source × phytase interaction. Feed intake, BW gain, and livability were reduced and FCR was higher in broilers fed low-avP diets, particularly in the presence of high phytate. Phytase A or phytase B improved feed intake, BW gain, and FCR, particularly in the high-phytate diet. However, broilers fed phytase A ate more and were heavier than broilers fed phytase B. Tibia ash was lowest in broilers fed the low-avP diet and highest in broilers fed the diet supplemented with mono-dicalcium phosphate. Phytase increased tibia ash, and broilers fed phytase A had an increase in tibia ash compared with broilers fed phytase B. In conclusion, high dietary phytate reduced broiler performance. Phytase A and phytase B improved bone ash and growth performance, especially in the high-phytate diets. However, phytase A was more efficacious than phytase B, regardless of the level of phytate.     

Sampling duration and freezing temperature influence the analysed gastric inositol phosphate composition of pigs fed diets with different levels of phytase

This experiment was conducted to determine the effects of time and freezing temperature during sampling on gastric phytate (myo-inositol [MYO] hexakisphosphate [InsP₆]), lower inositol phosphates (InsP_2–5) and MYO concentrations in pigs fed diets containing different levels of phytase. Forty pigs were fed 1 of 4 wheat-barley diets on an ad libitum basis for 28 d. The diets comprised a nutritionally adequate positive control (PC), a similar diet but with Ca and P reduced by 1.6 and 1.24 g/kg, respectively (NC), and the NC supplemented with 500 (NC + 500) or 2,000 (NC + 2000) FTU phytase/kg. At the end of the experiment, chyme were collected from the stomach, thoroughly mixed and 2 subsamples (30 mL) were frozen immediately: one snap-frozen at −79 °C and the other at −20 °C. The remaining chyme were left to sit at room temperature (20 °C) and further subsamples were collected and frozen as above at 5, 10 and 15 min from the point of mixing. There were linear reductions in gastric InsP₆ concentration over time during sampling (P < 0.001), irrespective of diet or freezing temperature. Moreover, InsP₆ concentration was influenced by a diet × freezing temperature interaction (P < 0.05), with less InsP₆ measured in chyme frozen at −20 °C than at −79 °C; however, this difference was greater in the control diets than the phytase supplemented diets. Freezing chyme at −79 °C recovered more ∑InsP_2–5 + MYO than freezing at −20 °C in pigs fed phytase supplemented diets; however, this difference was not apparent in the diets without phytase (diet × freezing temperature, P < 0.01). It can be concluded that significant phytate hydrolysis occurs in the gastric chyme of pigs during sampling and processing, irrespective of supplementary phytase activity. Therefore, to minimise post-slaughter phytate degradation and changes in the gastric inositol phosphate profile, chyme should be snap-frozen immediately after collection.     

Degradation of phytate in the gut of pigs--pathway of gastro-intestinal inositol phosphate hydrolysis and enzymes involved.

The present study gives an overview on the whole mechanism of phytate degradation in the gut and the enzymes involved. Based on the similarity of the human and pigs gut, the study was carried out in pigs as model for humans. To differentiate between intrinsic feed phytases and endogenous phytases hydrolysing phytate in the gut, two diets, one high (control diet) and the other one very low in intrinsic feed phytases (phytase inactivated diet) were applied. In the chyme of stomach, small intestine and colon inositol phosphate isomers and activities of phytases and alkaline phosphatases were determined. In parallel total tract phytate degradation and apparent phosphorus digestibility were assessed. In the stomach chyme of pigs fed the control diet, comparable high phytase activity and strong phytate degradation were observed. The predominant phytate hydrolysis products were inositol phosphates, typically formed by plant phytases. For the phytase inactivated diet, comparable very low phytase activity and almost no phytate degradation in the stomach were determined. In the small intestine and colon, high activity of alkaline phosphatases and low activity of phytases were observed, irrespective of the diet fed. In the colon, stronger phytate degradation for the phytase inactivated diet than for the control diet was detected. Phytate degradation throughout the whole gut was nearly complete and very similar for both diets while the apparent availability of total phosphorus was significantly higher for the pigs fed the control diet than the phytase inactivated diet. The pathway of inositol phosphate hydrolysis in the gut has been elucidated.     

Digestibility of phosphorus by growing pigs of fermented and conventional soybean meal without and with microbial phytase

An experiment was conducted to test the hypothesis that the apparent total tract digestibility (ATTD) and the standardized total tract digestibility (STTD) of P in fermented soybean meal (FSBM) are greater than in conventional soybean meal (SBM-CV) when fed to growing pigs. Four diets were formulated to contain FSBM or SBM-CV and either 0 or 800 units/kg of microbial phytase. The only sources of P in these diets were FSBM and SBM-CV. A P-free diet to estimate basal endogenous losses of P was also formulated. Thirty barrows (initial BW: 14.0 ± 2.3 kg) were placed in metabolism cages and allotted to 5 diets in a randomized complete block design with 6 pigs per diet. Feces were collected for 5 d after a 5-d adaptation period. All samples of ingredients, diets, and feces were analyzed for P, and values for ATTD and STTD of P were calculated. Results indicated that the basal endogenous P losses were 187 mg/kg of DMI. As phytase was added to the diet, the ATTD and STTD of P increased (P < 0.01) from 60.9 to 67.5% and from 65.5 to 71.9%, respectively, in pigs fed FSMB. Likewise, addition of phytase to SBM-CV increased (P < 0.01) the ATTD and STTD of P from 41.6 to 66.2% and from 46.1 to 71.4%, respectively. The ATTD and STTD of P were greater (P < 0.01) in FSBM than in SBM-CV when no phytase was used, but that was not observed when phytase was added to the diet (soybean meal × phytase interaction, P < 0.01). In conclusion, the ATTD and STTD of P in FSBM was greater than SBM-CV when no microbial phytase was added, but when phytase was added to the diets, no differences between FSBM and SBM-CV were observed in the ATTD and STTD of P.     

小麦日粮中木聚糖酶和植酸酶对肉仔鸡生长和养分消化率的影响

432只艾维因肉仔鸡用于研究小麦基础日粮中添加木聚糖酶(320FXU/kg)或添加750U/kg植酸酶降低日粮中0.08％的非植酸磷后,对生长性能、日粮表观代谢能、粗蛋白和植酸磷表观消化率的影响。试验结果表明:无论是单一添加木聚糖酶或植酸酶,还是同时添加这两种酶,都能提高1-6周龄肉仔鸡的增重和饲料转化率,降低死亡率。添加木聚糖酶可提高肉仔鸡小麦日粮的表观代谢能2.14％,增加氮的存留量2.58％。750U/kg的植酸酶完全可以降低肉仔鸡小麦日粮中0.08％非植酸磷。添加植酸酶的处理组可提高植酸磷的表观消化率43.25％,减少植酸磷排泄量55.0％。植酸酶和木聚糖酶对全期饲料转化率和植酸磷的表观消化率表现有明显的正互作效应(P<0.05)。