Hostname: page-component-848d4c4894-nr4z6 Total loading time: 0 Render date: 2024-05-26T22:09:16.731Z Has data issue: false hasContentIssue false

Replacement of zinc sulphate by microbial phytase for piglets given a maize-soya-bean meal diet

Published online by Cambridge University Press:  09 March 2007

C. Jondrevillea*
Affiliation:
Institut National de la Recherche Agronomique, Unité Mixte de Recherches INRA-Agrocampus Rennes d'Elevage, Nutrition Animale et Humaine, 35590 Saint-Gilles, France
R. Hayler
Affiliation:
BASF AG, E-MME/A Rheincenter 5. OG, 67056 Ludwigshafen, Germany
D. Feuerstein
Affiliation:
BASF AG, E-MME/A Rheincenter 5. OG, 67056 Ludwigshafen, Germany
Get access

Abstract

Forty-eight pigs, weaned at 27 days of age at an average body weight of 7·55 kg were used in a 19-day experiment to investigate the influence of microbial phytase on zinc utilization and to calculate equivalency values of zinc as sulphate for microbial phytase. Eight experimental diets were formulated: a maize-soya-bean meal basal diet containing 30 mg of zinc per kg supplemented with 10, 25, 40 or 100 mg of zinc from sulphate (ZnSO4, 7H2O) per kg or with 100, 250, 500 or 750 units (U) of microbial phytase (3- phytase from Aspergillus niger, Natuphos ®) per kg. The dietary supplies of calcium and phosphorus were adjusted accounting for the release of these elements by microbial phytase. The copper concentration in the diets was 11 mg/kg. Pigs were given the basal diet for a 7-day adjustment period prior to the 19-day experimental period. At the end of the experiment, bone ash, phosphorus and calcium concentrations as well as plasma and liver copper concentrations were independent of the diet (P > 0·10). The zinc status of piglets was assessed through plasma alkaline phosphatase activity (APA) and zinc concentration, bone zinc concentration and liver zinc concentration. Plasma zinc, plasma APA and bone zinc increased linearly (P < 0·001) and quadratically (P < 0·01, P < 0·001 and P < 0·001, respectively) with zinc added. These parameters also increased linearly (P < 0·001) and quadratically (P < 0·05, P < 0·001 and P < 0·05, respectively) with phytase added. Liver zinc increased quadratically (P < 0·05) with zinc added and tended to increase linearly with phytase added (P = 0·077). Linear and non-linear response equations of indicators of zinc status to zinc added and phytase added were developed and used to calculate zinc equivalency values of phytase. Non-linear models were linear plateau models for zinc added and exponential models for phytase added. Plasma APA, plasma zinc and bone zinc were maximized when zinc added reached 43, 54 and 56 mg/kg of diet, respectively. The mean function of equivalency of zinc as sulphate (Zn, mg/kg of diet) for microbial phytase (Phyt, U per kg of diet) was Zn = 49·9 − 58·3 e−0·00233Phyt. From this equation it is calculated that 250, 500, and 750 U of 3-phytase from Aspergillus niger can avoid the addition of 17, 32 and 40 mg of zinc as sulphate in a piglet diet. Zinc ingested and, in turn, zinc excreted, may be proportionately reduced by almost 0·30 by replacing 30 mg of zinc as sulphate by 500 U of phytase as Natuphos ® in a piglet maize and soya-bean meal diet formulated to contain 100 mg of zinc per kg.

Keywords

Type
Research Article
Copyright
Copyright © British Society of Animal Science 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adeola, O., Lawrence, B. V., Sutton, A. L. and Cline, T. R. 1995. Phytase-induced changes in mineral utilization in zinc-supplemented diets for pigs. Journal of Animal Science 73: 33843391.CrossRefGoogle ScholarPubMed
Davies, N. T. and Nightingale, R. 1975. The effects of phytate on intestinal absorption and secretion of zinc, and whole body retention of zinc, copper, iron and manganese in rats. British Journal of Nutrition 34: 243258.CrossRefGoogle ScholarPubMed
Engelen, A. J., Heeft, F. C. van der, Randsdorp, P. H. G. and Smit, E. L. C. 1994. Simple and rapid determination of phytase activity. Journal of AOAC International 77: 760764.CrossRefGoogle ScholarPubMed
Hill, D. A., Peo, E. R. Jr, Lewis, A. J. and Crenshaw, J. D. 1986. Zinc-amino acid complexes for swine. Journal of Animal Science 63: 121130.CrossRefGoogle ScholarPubMed
Institut National de la Recherche Agronomique. 1989. L'alimentation des animaux monogastriques: porc, lapin, volailles. INRA, Paris.Google Scholar
Institut National de la Recherche Agronomique – Association Française de Zootechnie. 2004. Tables of composition and nutritional value of feed materials. Pigs, poultry, cattle, sheep, goats, rabbits, horses, fish (ed. Sauvant, D., Perez, J. M. and Tran, G.), INRA-AFZ, Paris.CrossRefGoogle Scholar
Jondreville, C., Revy, P. S. and Dourmad, J. Y. 2003. Dietary means to better control the environmental impact of copper and zinc by pigs from weaning to slaughter. Livestock Production Science 84: 147156.CrossRefGoogle Scholar
Kornegay, E. T. 2001. Digestion of phosphorus and other nutrients: the role of phytases and factors influencing their activity. In Enzymes in farm animal nutrition (ed. Bedford, M. R. and Partridge, G. G.), pp. 237271. CAB International, Wallingford.CrossRefGoogle Scholar
Kornegay, E. T. and Qian, H. 1996. Replacement of inorganic phosphorus by microbial phytase for young pigs fed on a maize-soyabean-meal diet. British Journal of Nutrition 76: 563578.Google Scholar
Lei, X. G., Ku, P. K., Miller, E. R., Ullrey, D. E. and Yokoyama, M. T. 1993. Supplemental microbial phytase improves bioavailability of dietary zinc to weanling pigs. Journal of Nutrition 123: 11171123.Google ScholarPubMed
Miller, E. R., Luecke, R. W., Ullrey, D. E., Baltzer, B. V., Bradley, B. L. and Hoefer, J. A. 1968. Biochemical, skeletal and allometric changes due to zinc deficiency in the baby pig. Journal of Nutrition 95: 278286.Google Scholar
Mills, C. F. 1985. Dietary interactions involving the trace elements. Annual Reviews of Nutrition 5: 173193.CrossRefGoogle ScholarPubMed
National Research Council. 1998. Nutrient requirements of swine, 10th edition. NRC, National Academy Press, Washington, DC.Google Scholar
Oberleas, D. and Harland, F. 1996. Impact of phytic acid on nutrient availability. In Phytase in animal nutrition and waste management (ed. Coelho, M. B. and Kornegay, E. T.), pp. 7784. BASF, Mount Olive, NJ.Google Scholar
Oberleas, D., Muhrer, M. E. and O'Dell, B. L. 1962. Effects of phytic acid on zinc availability and parakeratosis in swine. Journal of Animal Science 21: 5761.CrossRefGoogle Scholar
Oberleas, D., Muhrer, M. E. and O'Dell, B. L. 1966. Dietary metal-complexing agents and zinc availability in the rat. Journal of Nutrition 90: 5662.CrossRefGoogle ScholarPubMed
O'Dell, B. L. and Savage, J. E. 1960. Effect of phytic acid on zinc availability. Proceedings of the Society for Experimental Biology and Medicine 103: 304306.CrossRefGoogle ScholarPubMed
Pallauf, J., Höhler, D. and Rimbach, G. 1992. Effect of microbial phytase supplementation to a maize-soya-diet on the apparent absorption of Mg, Fe, Cu, Mn and Zn and parameters of Zn-status in piglets. Journal of Animal Physiology and Animal Nutrition 68: 19.Google Scholar
Pallauf, J., Rimbach, G., Pippig, S., Schindler, B., Höhler, D. and Most, E. 1994. Dietary effect of phytogenic phytase and an addition of microbial phytase to a diet based on field beans, wheat, peas and barley on the utilization of phosphorus, calcium, magnesium, zinc and protein in piglets. Zeitschrift für Ernährungswissenschaft 33: 128135.Google Scholar
Rapp, C., Lantzsch, H. J. and Drochner, W. 2001. Hydrolysis of phytic acid by intrinsic plant or supplemented microbial phytase (Aspergillus niger) in the stomach and small intestine of minipigs fitted with re-entrant cannulas. 3. Hydrolysis of phytic acid (IP6) and occurrence of hydrolysis products (IP5, IP4, IP3 and IP2). Journal of Animal Physiology and Animal Nutrition 85: 420430.CrossRefGoogle ScholarPubMed
Revy, P. S., Jondreville, C., Dourmad, J. Y. and Nys, Y. 2004. Effect of zinc supplemented as either an organic or an inorganic source and of microbial phytase on zinc and other minerals utilisation by weanling pigs. Animal Feed Science and Technology 116: 93112.CrossRefGoogle Scholar
Revy, P. S., Jondreville, C., Dourmad, J. Y. and Nys, Y. 2005. Assessment of dietary zinc requirement of weaned piglets fed diets with or without microbial phytase. Journal of Animal Physiology and Animal Nutrition In press.Google Scholar
Schell, T. C. and Kornegay, E. T. 1996. Zinc concentration and performance of weanling pigs fed pharmacological levels of zinc from ZnO, Zn-methionine, Zn-lysine or ZnSO4. Journal of Animal Science 74: 15841593.CrossRefGoogle ScholarPubMed
Simons, P. C. M., Versteegh, H. A. J., Jongbloed, A. W., Kemme, P. A., Slump, P., Bos, K. D., Wolters, M. G. E., Beudeker, R. F. and Verschoor, G. J. 1990. Improvement of phosphorus availability by microbial phytase in broilers and pigs. British Journal of Nutrition 64: 525540.Google Scholar
Statistical Analysis Systems Institute. 2000. Software package version 8·1. SAS Institute, Cary, NC.Google Scholar
Underwood, E. J. and Suttle, N. F. 1999. The mineral nutrition of livestock, third edition. CAB International, NY.Google Scholar
Wedekind, K. J., Lewis, A. J., Giesemann, M. A. and Miller, P. S. 1994. Bioavailability of zinc from inorganic and organic sources for pigs fed corn-soybean meal diets. Journal of Animal Science 72: 26812689.CrossRefGoogle ScholarPubMed
Wise, A. and Gilburt, D. 1982. In vitro competition between calcium phytate and the soluble fraction of rat small intestine contents for cadmium, copper and zinc. Toxicology Letters 11: 4954.CrossRefGoogle ScholarPubMed
Yi, Z., Kornegay, E. T., Ravindran, V., Lindemann, M. D. and Wilson, J. H. 1996. Effectiveness of Natuphos phytase in improving the bioavailabilities of phosphorus and other nutrients in soybean meal-based semipurified diets for young pigs. Journal of Animal Science 74: 16011611.CrossRefGoogle ScholarPubMed
Zacharias, B., Ott, H. and Drochner, W. 2003. The influence of dietary microbial phytase and copper on copper status in growing pigs. Animal Feed Science and Technology 106: 139148.CrossRefGoogle Scholar