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Query: EC:3.1.3.8 (phytase)
 1,997 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

One of the myoinositol trisphosphates produced by the phytase-myoinositol hexakisphosphate (InsP6) reaction is Ins(2,4,5)P3. That Ins(2,4,5)P3 can elicit Ca2+ mobilization from intracellular stores in plants [Samanta, S., Dalal, B., Biswas, S., & Biswas, B.B.(1993) Biochem. Biophys. Res. Commun. 191,427] prompted us to elucidate the mechanism. The InsP3 [Ins(1,4,5)P3/Ins(2,4,5)P3]-phytase complex has been found to interact with the receptor for InsP3 in vitro forming a ternary complex, and a nanomolar concentration of InsP3 is required. For enzymatic cleavage of InsP3 by phytase, micromolar concentrations are needed, and the affinities of the phytase for different myoinositol phosphates have been found to depend upon the number of phosphate groups present in the substrate. Fraction accessibility of tryptophan residues to a neutral fluorescence quencher, acrylamide in free and myoinositol phosphates bound phytase, as determined by Stern-Volmer plot, records a progressive decrease starting from InsP6 to InsP with the notable exceptions of both Ins (1,4,5)P3 and Ins(2,4,5)P3. This deviation from the trend of change in the accessibility of tryptophan residues in myoinositol phosphate bound phytase is recorded from the fact that there is a high affinity (dissociation constant of the nanomolar order) and noncatalytic binding site in phytase for the two isomers of InsP3. In the nanomolar range of concentrations, both isomers of InsP3 bind to a second site of phytase having about 40-fold higher affinity than the normal substrate binding site. InsP3, when bound to noncatalytic site in phytase is not hydrolyzed but induces a significant change in the conformation of phytase as assayed from the relative accessibility of tryptophan residues. This conformational change in phytase is recognized by the receptor for InsP3, because in absence of InsP3 no interaction between the receptor and phytase is detected. However, InsP3-phytase complex is a better elicitor of Ca2+ efflux from microsomal/vacuolar fractions than free InsP3. This is further confirmed by the fact that when Ins(1,3,4)P3-phytase complex can elicit Ca2+ efflux from intracellular stores, Ins(1,3,4)P3 per se is minimally effective.
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PMID:Interaction of myoinositoltrisphosphate-phytase complex with the receptor for intercellular Ca2+ mobilization in plants. 866 92

Three groups of individually housed albino rats (n = 6, initial average weight = 47 g) were fed diets based on egg white and cornstarch (basal diet 8 g Ca, 5.2 g P, 0.76 g Mg, 100 mg Zn, 100 mg Fe, 50 mg Mn, 7 mg Cu, and 5 mg Cd per kilogram diet) over a 4-week period. Group I (controls) was fed the basal diet free of phytic acid (PA) and microbial phytase. In groups II and III cornstarch was replaced by 0.5% PA from NaPA (molar PA/Zn ratio approximately 5). In group III, 2,000 U of microbial phytase from Aspergillus niger per kilogram diet was added. Live weight gain, zinc status (zinc in plasma, femur, liver, and testes; activity of the plasma alkaline phosphatase), and apparent absorption of zinc, iron, copper, and manganese remained unchanged by the different dietary treatments. The apparent phosphorus absorption was highest in the phytase group. PA decreased and microbial phytase improved the apparent absorption of calcium and magnesium. Liver cadmium concentration, total liver and kidney cadmium content, as well as fractional liver and kidney cadmium accumulation in rats fed the diet containing PA were significantly higher than those in the controls. Phytase supplementation lowered liver and kidney cadmium accumulation. Differences in calcium and magnesium bioavailability due to PA and microbial phytase may be one factor in the alteration of tissue cadmium accumulation.
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PMID:Effect of phytic acid and microbial phytase on Cd accumulation, Zn status, and apparent absorption of Ca, P, Mg, Fe, Zn, Cu, and Mn in growing rats. 867 72

2 x 6 pigs continuously housed in metabolic cages from 25-100 kg weight were fed N-reduced diets based on barley, maize and soybean meal. Diet I (control) contained in FM (fresh matter) 0.56%, 0.48% and 0.46% P (feeding phases A: 25-50 kg, B: 50-75 kg, C: 75-100 kg weight) and 0.76%, 0.71% and 0.68% Ca. Diet II was low in P (0.46%, 0.40%, 0.32%) and Ca (0.69%, 0.62%, 0.52%) and 800 U Aspergillus-phytase per kg were added. Analyzed cadmium concentrations in diet I were 23.4, 19.9 and 13.7 micrograms/kg FM and 20.6, 14.9 and 12.7 micrograms/kg FM in diet II respectively. At 100 kg weight in both treatment groups low cadmium concentrations in liver (11.8 vs. 17.3 micrograms Cd/kg FM) and kidneys (59.6 vs. 102 micrograms Cd/kg FM) were found. Contrary to findings for rats fed semisynthetic diets enriched with high CdCl2 levels, phytase supplementation to the P- and Ca-reduced pig diet with a low Cd concentration significantly enhanced liver and kidney cadmium accumulation. Differences in dietary Cd levels, the binding form of Cd in the diets and the duration of the experimental trials may partially explain the differences found between rats and pigs. Complex interactions between cadmium and various elements, especially calcium, might also have additionally influenced the carry over of cadmium in the present study. Irrespective of the dietary treatment, liver and kidney cadmium concentrations in both groups were considerably lower than maximal permitted values.
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PMID:Effect of microbial phytase on cadmium accumulation in pigs. 898 14

This experiment was conducted to measure the nutritional and metabolic responses of pigs fed diets with continuous supplementation of microbial and cereal phytase from weaning to finishing, and to determine the feasibility of complete replacement of inorganic P addition by supplemental phytase in swine diets. Forty-eight Landrace x Hampshire x Meishan pigs were divided into four groups. In phase 1 (10 to 50 kg BW), pigs in Groups 1, 2, 3, and 4 were fed a low-P, corn-soybean meal basal diet (BD), the BD plus microbial phytase (A. ficuum) at 1,200 units/kg, the BD plus 10% wheat bran (230 units of cereal phytase/kg), and the BD + .24% inorganic P (calcium phosphate), respectively. In phase 2 (51 to 90 kg BW), these pigs were fed a similar BD or the BD plus 1,000 microbial phytase units/kg, 20% wheat bran, or .20% inorganic P, respectively. Repeated measures included growth performance, P, Ca, and N balance, metatarsal and metacarpal bone strength, serum concentration of inorganic P, Ca, and 1,25-dihydroxycholecalciferol, and serum alkaline phosphatase activity. Pigs fed the BD supplemented with microbial phytase and pigs fed the BD supplemented with inorganic P showed almost identical responses for all variables. Pigs fed the BD supplemented with cereal phytase also had responses for various measures that were similar to those of pigs fed microbial phytase or inorganic P, except for some differences in serum inorganic P concentrations and bone strength in phase 1. Because of improvements in apparent digestibility of dietary P and N, fecal excretion of these two nutrients was reduced by 31 to 62% (P < .05) in pigs fed the BD supplemented with phytase compared with pigs fed inorganic P. It is physiologically feasible and environmentally advantageous to replace inorganic P with microbial or cereal phytase in corn-soybean meal diets for this type of pig through the entire growing-finishing period.
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PMID:Supplemental phytases of microbial and cereal sources improve dietary phytate phosphorus utilization by pigs from weaning through finishing. 911 Feb 15

A 17-wk study was conducted to evaluate the effects of supplementing laying hen diets with a commercially produced microbial phytase. Hy-Line W-36 pullets (21 wk of age) were randomly allocated to 1 of 10 diets in a factorial arrangement of five levels of nonphytate phosphorus (0.1 to 0.5% NPP) and two levels of phytase (0 and 300 U/kg feed). Dietary metabolizable energy, protein, and calcium were maintained at 2,816 kcal/kg, 16.6%, and 4%, respectively. Criteria evaluated included egg production, feed consumption, egg weight, egg specific gravity, mortality, and various bone quality parameters. Feeding 0.1% NPP without supplemental phytase decreased egg production (hen-housed) 8.1% over the entire study and 29.6% over the last 4 wk, relative to other diets without supplemental phytase. Similarly, feed consumption of hens fed 0.1% NPP without phytase decreased 5.8% over 17 wk and 13.0% over the last 4 wk. Egg production and feed consumption were maintained at the level of other treatments without phytase when the 0.1% NPP diet was supplemented with phytase (82.1% and 82.4 g per hen per d, respectively). Egg weights and egg specific gravity decreased and mortality increased when hens consumed 0.1% NPP without phytase. Supplementing the 0.1% NPP diet with phytase completely corrected these adverse effects. No deficiency symptoms were observed in hens fed diets containing 0.2 to 0.5% NPP. Phytase supplementation of these diets gave no further improvements in performance.
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PMID:Performance of commercial laying hens fed various phosphorus levels, with and without supplemental phytase. 925 Nov 48

The extracellular activity of Aspergillus niger phytase at the end of the growth phase was 132 nkat/mL in a laboratory bioreactor. The purified enzyme has molar mass approximately 100 kDa, pH optimum at 5.0, temperature optimum at 55 degrees C and high pH and temperature stability. The Km for dodecasodium phytate, calcium phytate and 4-nitrophenyl phosphate are 0.44, 0.45 and 1.38 mmol/L, respectively. The enzyme is noncompetively inhibited by inorganic monophosphate (Ki = 2.85 mmol/L) and by Cu2+, Zn2+, Hg2+, Sn2+, Cd2+ ions and strongly by F- ones; it is activated by Ca2+, Mg2+ and Mn2+ ions. The substrate specificity of phytase is broad with the highest affinity to calcium phytate.
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PMID:Characterization of phytase produced by Aspergillus niger. 944 82

The Bacillus subtilis strain VTT E-68013 was chosen for purification and characterization of its excreted phytase. Purified enzyme had maximal phytase activity at pH 7 and 55 degrees C. Isolated enzyme required calcium for its activity and/or stability and was readily inhibited by EDTA. The enzyme proved to be highly specific since, of the substrates tested, only phytate, ADP, and ATP were hydrolyzed (100, 75, and 50% of the relative activity, respectively). The phytase gene (phyC) was cloned from the B. subtilis VTT E-68013 genomic library. The deduced amino acid sequence (383 residues) showed no homology to the sequences of other phytases nor to those of any known phosphatases. PhyC did not have the conserved RHGXRXP sequence found in the active site of known phytases, and therefore PhyC appears not to be a member of the phytase subfamily of histidine acid phosphatases but a novel enzyme having phytase activity. Due to its pH profile and optimum, it could be an interesting candidate for feed applications.
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PMID:Isolation, characterization, molecular gene cloning, and sequencing of a novel phytase from Bacillus subtilis. 960 17

Crossbred weanling pigs (an equal number of barrows and gilts) with an average initial weight of 7.4 (Exp. 1) or 9.6 kg (Exp. 2) were used in two 4-wk experiments (Exp. 1, n = 96; Exp. 2, n = 96) to investigate the effects of added phytase or citric acid on performance, rib mineralization, gastric pH, and digestibility measurements. A corn-soybean meal-based diet low in Ca and P was used in both experiments. In Exp. 1, three citric acid levels (0, 1.5, or 3.0%) and four phytase levels (0, 250, 500, or 750 U/kg) were used in a 3 x 4 factorial arrangement of treatments. In Exp. 2, two citric acid levels (0 or 2.0%) and three phytase levels (0, 250, or 500 U/kg) were used in a 2 x 3 factorial arrangement of treatments. Phosphorus was maintained at .33 and .34% in Exp. 1 and 2, respectively. Calcium was maintained at a 2.5:1 ratio with total available P (available P plus the estimated released phytate P by phytase) in Exp. 1 and at a level of .44% in Exp. 2. In both experiments, BW and feed consumption were measured weekly, and pen fecal samples were collected twice daily for 5 d during wk 4. At the end of wk 4, the barrow in each pen was killed following a fast-refeed-fast (22-1-2 h) regimen for collection of 10th ribs and stomach digesta. In Exp. 1 and 2, phytase addition did not affect (P > .05) performance but linearly increased (P < .05) rib shear force, shear energy, dry bone weight, ash weight, ash percentage, and Ca and P digestibilities. Addition of citric acid in both experiments reduced dietary pH and stomach digesta pH (P < .05). The addition of citric acid improved (P < .05) ADG, feed efficiency, and Ca digestibility in Exp. 1, but it had no effect on performance and Ca digestibility in Exp. 2. In summary, the additions of citric acid and phytase to weanling pig diets were each beneficial, but no synergistic effects were observed.
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PMID:The effects of microbial phytase, citric acid, and their interaction in a corn-soybean meal-based diet for weanling pigs. 969 Jun 44

A feeding trial was performed using 4 x 60 day-old chickens (Ross 208 cockerels) raised up to 42 days of age to determine whether exogenous phytase addition increases phosphorus utilisation by broiler chickens, and to assess its effects on some production traits as well as on the ash content and mechanical stability of the tibia. The chickens' feed consisted of maize, wheat, soybean meal, fish meal, yeast, and fat powder. The basic feed was supplemented with inorganic phosphorus in groups A and B. In groups C and D, the amount of the inorganic phosphorus supplement (DCP) was decreased by 50%, at the same calcium/phosphorus ratio. The 50% reduction of inorganic phosphorus supplementation represents a 20% decrease of total phosphorus. To the diets of groups B and D a phytase enzyme preparation (Phytase Novo CT) was added. The calculated exogenous phytase activity was 600 FYT/kg feed. The decrease of inorganic phosphorus did not cause significant differences in the daily weight gain but lowered the feed conversion rate by 10%. Calcium and phosphorus excretion decreased by 18% and 15%, and the breaking strength of the tibia was also lower. Phytase supplementation of the feed at a lower rate of inorganic phosphorus supplementation did not cause changes in the body weight gain but improved the feed conversion rate by 5.6%. Phosphorus and calcium output decreased by 21% and 11%, respectively, but chemical composition and mechanical stability of the tibia were unaltered.
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PMID:Effects of phytase supplementation on calcium and phosphorus output, production traits and mechanical stability of the tibia in broiler chickens. 970 26

Three experiments were conducted with 96 growing Landrace x Yorkshire x Duroc crossbreds to determine the collective effectiveness of cereal phytase from wheat middlings, microbial phytase, and citric acid in improving phytate-P bioavailability in corn-soy diets. In Exp. 1, 40 gilts (7 wk old) were fed five diets for 8 wk. Diets 1, 2, and 3 were low-P, corn-soybean meal diets (CSB) + 0, .1, or .2% inorganic P (Pi) as calcium phosphate, respectively. Diet 4 was a similar corn-soy diet that included 15% wheat middlings (461 cereal phytase U/kg). Diet 5 was the CSB + microbial phytase (1,200 U/kg; Natuphos, BASF, Mount Olive, NJ). In Exp. 2, 16 barrows (8 wk old) were fed two diets for 6 wk. Diet 1 was the same as Diet 3 of Exp. 1 (.2% Pi). Diet 2 was Diet 4 of Exp. 1 + microbial phytase (300 U/kg). In Exp. 3, 40 barrows and gilts (6 wk old) were fed four diets for 6 wk. Diets 1 and 2 were the same as those in Exp. 2. Diet 3 was Diet 2 of Exp. 2 + 1.5% citric acid. Diet 4 was similar to Diet 3 but contained 10 instead of 15% wheat middlings. In Exp. 1, pigs fed the low-P, CSB (Diet 1) had lower (P < .05) ADG, ADFI, plasma Pi concentration, bone strength, and mobility score than pigs of the other four treatments. Measurements for pigs fed the 15% wheat middlings diet were not significantly different from those of pigs fed the CSB + .1% Pi or microbial phytase. In Exp. 2, ADG (P=.06) during wk 1 to 3 and gain:feed ratio (P < .02) and plasma Pi concentration (P < .005) during all weeks favored pigs fed the CSB + .2% Pi compared with the other diet including 15% wheat middlings. In Exp. 3, identical ADG during all weeks and similar plasma Pi concentrations at wk 4 and 6 were observed between pigs fed the two citric acid diets (Diets 3 and 4) and the CSB + .2% Pi (Diet 1). Pigs fed Diet 4 (10% wheat middlings) had even higher (P < .02) gain:feed ratio during wk 1 to 3 than those fed Diet 1. It seems feasible to completely replace calcium phosphate with 10 to 15% wheat middlings, 300 U microbial phytase/ kg, and 1.5% citric acid in the corn-soy diets for growing pigs.
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PMID:Adding wheat middlings, microbial phytase, and citric acid to corn-soybean meal diets for growing pigs may replace inorganic phosphorus supplementation. 981 6


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