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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)

Two generations of red cells (embryonic and definitive), different types of haemoglobins, and special organic phosphates involved in the control of haemoglobin oxygenation (2:3-bisphosphoglycerate, BPG, and inositol-5-phosphate, IP5), have been found progressively during development of the chick. Levels of both organic phosphates, as well as activities of the enzymes involved in BPG synthesis (2:3-bisphosphoglycerate synthase, BPGM) and IP5 formation (phytase), were studied in the erythrocyte populations from embryo, young and adult chickens. Measurement of specific activities of BPGM and phytase in the two subpopulations present in young chickens showed that these phosphates could be specifically and predominantly formed in these two red cell populations.
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PMID:Synthesis and levels of organic phosphates in erythrocytes during avian development: specific formation of BPG and IP5 in two distinct populations from young chicks. 609 74

The effects of whole wheat bran and its components on the absorption of nonheme dietary iron were measured using a double isotope technique in human volunteers. When 12 g bran was added to a light meal, absorption decreased by 51 to 74%; this inhibitory effect of bran was shown for meals of both high and low iron availability. Inhibition was not explained by monoferric phytate, the major form of iron in bran, because labeled iron from monoferric phytate was absorbed at least as well as the common pool of nonheme dietary iron. Furthermore, removal of phytate from bran by endogenous phytase did not in itself alter the inhibitory effect of the bran on iron absorption. Studies in which dephytinized bran was separated into a soluble, phosphate-rich fraction and an insoluble, high-fiber fraction indicated that the soluble fraction was more inhibitory than the insoluble fraction.
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PMID:The inhibitory effect of bran on iron absorption in man. 626 27

An enzyme which liberates Pi from myo-inositol hexaphosphate (phytic acid) was shown to be present in culture filtrates of Bacillus subtilis. It was purified until it was homogeneous by ultracentrifugation, but it still showed two isozymes on polyacrylamide gel electrophoresis. The enzyme differed from other previously known phytases in its metal requirement and in its specificity for phytate. It had a specific requirement for Ca2+ for its activity. The enzyme hydrolyzed only phytate and had no action on other phosphate esters tested. This B. subtilis phytase is the only known phytate-specific phosphatase. The products of hydrolysis of phytate by this enzyme were Pi and myo-inositol monophosphate. The enzyme showed optimum activity at pH 7.5. It was inhibited by Ba2+, Sr2+, Hg2+, Cd2+, and borate. Its activity was unaffected by urea, diisopropylfluorophosphate, arsenate, fluoride, mercaptoethanol, trypsin, papain, and elastase.
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PMID:Purification and properties of phytate-specific phosphatase from Bacillus subtilis. 628 90

In mammals, bisphosphoglycerate-synthase activity, whose assay methods are previously discussed, increases gradually along erythropoiesis, leading to a consequent enhancement of 2,3-bisphosphoglycerate formation. Avian erythrocytes, on the other hand, contain inositol-pentaphosphate as major organic phosphate starting from egg eclosion, which substitutes embrionary ATP and 2,3-BPG in the regulatory function. The IHP of phytase and the disappearance of 2,3-BPG synthesis, also inhibitor of enzyme activity, should be considered responsible for IPP accumulation.
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PMID:[Metabolism of the organic phosphate regulators of oxygenation in cells of the erythrocyte series in birds and mammals]. 629 20

An in vitro method was developed to predict inorganic P release from maize-soyabean poultry feeds containing supplemental phytase (EC 3.1.3.8), and to quantify the effect of acid phosphatase (EC 3.1.3.2), fungal protease (EC 3.4.23.6) and Aspergillus niger cellulase (EC 3.2.1.4) on phytate dephosphorylation. Pepsin (EC 3.4.23.1) and pancreatin digestion periods were preceded by a 30 min pre-incubation at pH 5.25 to simulate digestion in the crop of poultry. Pancreatin digestion was carried out in dialysis tubing, with a ratio of about 1:25 (v/v) between the digesta and dialysing medium, to simulate gradient absorption from the duodenum. The feed:water ratio was kept within physiological limits and a constant proportion of feed weight to digestive enzymes was maintained. There was a linear response to increasing dosages of phytase up to 1000 phytase units (FTU)/kg feed, and to increasing phosphate concentration in feeds. In vivo validation was performed with growing turkeys (1-3 weeks) fed on diets containing 12 g Ca/kg and 0, 500 or 1000 FTU phytase/kg in a factorial arrangement with 0, 1, 2 or 3 g supplemental phosphate/kg (from KH2PO4). After a simple transformation (variable/in vitro P = f (in vitro P)), amounts of P hydrolysed from feed samples by in vitro digestions correlated with 3-week body-weight gain (R 0.986, P < 0.0001), toe ash (R 0.952, P < 0.0001), feed intake (R 0.994, P < 0.0001) and feed efficiency (R 0.992, P < 0.0001). The dephosphorylating ability of phytase in vitro was significantly enhanced (P < 0.05) by the addition of acid phosphatase. Fungal acid protease and Aspergillus niger cellulase also enhanced the dephosphorylation process in vitro.
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PMID:An in vitro procedure for studying enzymic dephosphorylation of phytate in maize-soyabean feeds for turkey poults. 754 27

Three experiments involving 162 pigs were conducted to assess the efficacy of phytase (Natuphos; BASF, Mount Olive, NJ) in low-P, corn-soybean meal-based diets. The phytase was produced by a recombinant Aspergillus niger. The phytase supplement contained 5,000 phytase units (PTU)/g. In Exp. 1 (66 pigs) and 2 (60 pigs), growing-finishing pigs were fed fortified corn-soybean meal diets formulated to be adequate (.50%), marginal (.425%), or inadequate (.35%) in P during the growing phase (23 to 60 kg BW) followed by adequate (.40%), marginal (.35%), or inadequate (.30%) P, respectively, during the finishing phase (to 104 kg BW). Dicalcium phosphate was the source of supplemental P. In addition, the low-P sequence (.35/.30% P) was supplemented with phytase at 250, 500, or 1,000 PTU/kg. Rate and efficiency of gain decreased linearly (P < .01) and bone breaking strength decreased quadratically (P < .01) as the concentration of P was decreased in the diets. Responses in growth and bone traits to increasing levels of phytase activity in the low-P diet were linear (P < .01). The highest level of phytase in the low-P diet restored growth rate and bone breaking strength to levels that approached or met those of pigs fed the adequate P diet.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Efficacy of a recombinant-derived phytase in improving the bioavailability of phosphorus in corn-soybean meal diets for pigs. 759 84

Two experiments involving 115 pigs were conducted to assess the efficacy of a microbial phytase (Allzyme Phytase; Alltech, Nicholasville, KY) produced by Aspergillus niger in low-P, corn-soybean meal-based diets. The phytase supplement contained 50 phytase units/g and 1.43% P. In Exp. 1, growing-finishing pigs were fed fortified corn-soybean meal diets formulated to be adequate (.50%) or inadequate (.30%) in P during the growing phase (38 to 57 kg BW) followed by adequate (.40%) or inadequate (.30%) P, respectively, during the finishing phase (to 101 kg BW). Dicalcium phosphate was the source of supplemental P. Half the diets were supplemented with phytase at 500 phytase units/kg. Rate and efficiency of gain and bone breaking strength were decreased (P < .01) when the low-P diet was fed. Adding phytase to the low-P diet restored performance and bone breaking strength (P < .01) to levels that approached those of pigs fed the adequate-P diet. In Exp. 2, growing pigs (13 kg BW), were fed a low-P (.32% total P; .048% available P) based diet supplemented with graded levels of monosodium phosphate to provide 0, .075, and .15% added P or with phytase to supply 250, 500, 1,000, or 2,000 phytase units/kg. Chromic oxide was included as an indigestible marker for determining apparent absorption and fecal excretion of P. Performance and bone strength increased linearly with added monosodium phosphate (P < .01) and with increasing levels of supplemental phytase (P < .05). A portion of these increases from phytase was attributed to the P supplied by the phytase mix (.007, .014, .028, .057%, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Efficacy of low-activity, microbial phytase in improving the bioavailability of phosphorus in corn-soybean meal diets for pigs. 760 78

Four acid phosphatase (phosphomonoesterase E.C.3.1.3.2) genes were cloned by polymerase chain reaction (PCR). These were pho3, pho5 and pho11 from Saccharomyces cerevisiae and the gene for a phosphate-respressible acid phosphatase from Aspergillus niger. The individual genes were subcloned into an A. oryzae expression vector downstream from a starch-inducible alpha-amylase promoter and the resulting expression constructs were transformed into a mutant strain of A. oryzae, AO7. Southern hybridization analysis confirmed that the acid phosphatase genes had been integrated into the host genome with estimates of integrated copy numbers ranging from 2 to 20 for individual transformants. Northern hybridization analysis of total RNA from individual transformants revealed the presence of a single transcript of the expected size of 1.8 kb. Production of recombinant protein was induced by the addition of 30 g L-1 of soluble starch in the fermentation media. Active acid phosphatases, not present in control cultures, were detected in the supernatant fractions of transformant cultures by acid phosphatase activity staining of non-denaturing polyacrylamide gels. The ability of the recombinant acid phosphatases to hydrolyze phytate was assessed by referenced phytase (myoinositol hexakisphosphate phosphohydrolase E.C. 3.1.3.8) activity assay procedures. A two- to six-fold increase in phytase activity was measured in transformants compared to control, untransformed A. oryzae. Sufficient quantities of A. niger and pho5 recombinant acid phosphatases were generated from large-scale fermentations to assess the efficacy of these enzymes as phytate-degrading enzymes when included in poultry diets.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Molecular cloning, expression and evaluation of phosphohydrolases for phytate-degrading activity. 761 16

A high phytic acid diet (barley, wheat, soya bean meal, 4 g P/kg, of that 2/3 phytate P) without added phytase, with phytase supplement (1000 U/kg diet) or with supplementary phosphate (2,2g P/kg diet) was examined with 3 x 12 weaned piglets. The high dietary P level due to phosphate addition, significantly improved body weight gain and feed:gain ratio. The phytase effect on these criteria was small. The phytase but more the supplementary phosphate increased P concentration of serum. In case of phytase addition pigs had 10% less ash P and Ca in the rib than animals of phosphate group. In the group without phytase or P addition the ash, P and Ca concentration of bone were decreased by 20%.
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PMID:[Evaluation of Aspergillus niger phytase and dietary phosphate in weaned piglets. 1. Growth, blood serum and bone status]. 766 74

A high phytic acid diet (barley, wheat, soya bean meal, 4 g P/kg diet, of that 2/3 phytate P) without added phytase, with phytase supplement (1000 U/kg diet) or with supplementary phosphate (2.2 g P/kg diet) was examined with 3 x 12 weaned piglets. The three diets contained 8 g Ca/kg. At the end of experiment 6 pigs/group were slaughtered. In animal body (as empty body) the content and gain of ash, P, Ca, protein and fat were detected. P supplementation and supplementary phytase had no effect on dry matter, protein and fat content of animal body. The enzyme but more the supplementary phosphate increased mineralization of skeleton and made the animal body higher in ash, P and Ca content. Piglets without supplementary phytase and P gained 1.1 g P daily. Phytase increased daily P gain by 0.5 g (P < 0.05), the phosphate by 1.4 g (P < 0.001). The daily Ca gain was 1.7; 2.8 and 5.1 g in the different groups. A piglet (body weight 20 kg) with sufficient P and Ca in the diet gains 5 g P and 10 g Ca per kg body weight gain (empty body).
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PMID:[Evaluation of Aspergillus niger phytase and phosphate in weaned piglets. 2. Content and gain of fat, energy, ash, Ca and P in the animal body]. 766 82


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