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Interactions between dietary carbohydrate and nitrogen and digestion in sheep

Published online by Cambridge University Press:  27 March 2009

J. D. Oldham
Affiliation:
University of Nottingham, School of Agriculture, Sutton Bonington, Loughborough, Leics. LE12 5RD
P. J. Buttery
Affiliation:
University of Nottingham, School of Agriculture, Sutton Bonington, Loughborough, Leics. LE12 5RD
H. Swan
Affiliation:
University of Nottingham, School of Agriculture, Sutton Bonington, Loughborough, Leics. LE12 5RD
D. Lewis
Affiliation:
University of Nottingham, School of Agriculture, Sutton Bonington, Loughborough, Leics. LE12 5RD

Summary

Rumen fermentation, duodenal digesta flow and N balance were studied in three sheep fed diets which contained urea or fishmeal as nitrogen supplement and either barley straw, barley + corn starch or molassed wheat straw (60% molasses) as carbo-hydrate source.

The molar composition of rumen volatile fatty acids (VFA) with straw diets was high in acetate (64–68%), with barley diets high in propionate (32–36%) and with molasses diets high in butyrate (28–34%). Rumen ammonia concentrations (RAC) were low and constant with fishmeal diets (< 10 mM) but varied with carbohydrate source with urea diets. RAC was very high (24 mM) after feeding molasses + urea.

With barley and molasses diets 73–75% of digestible dry matter (DDM) was digested in the stomach, but only 54–59% with ground and pelleted straw diets. For all diets less N passed the duodenum than was eaten. The lowest daily duodenal N passage was with molasses + urea. Daily urinary N output was highest (P < 0·01) for this diet and nitrogen balance lowest.

Daily intakes of amino acids differed widely between diets but differences in duodenal passage were not so great. Molasses + urea provided the lowest values for daily duodenal amino acid flow. The amino acid content of duodenal N (mM amino acid/16 g N) was relatively constant despite broad variation between diets. Digesta alanine and valine (mM/16 g N) were higher for barley than for straw diets (P < 0·05). Digesta methionine (mM/16 g N) was lower for fishmeal than for urea diets (P < 0·01).

Very little sucrose reached the duodenum with any diet.

It was concluded that the form of energy-yielding nutrient inuflenced duodenal N flow by affecting ammonia-N capture in the rumen, but that the amino acid content of duodenal N was little affected. The interaction between molasses and urea was not beneficial to efficient use of urea-N in this work when molasses was the major carbohydrate component of the diet.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1977

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References

Agricultural Research Council (1965). Nutrient Requirements of Farm Livestock. No. 3. Ruminants. London: H.M.S.O.Google Scholar
Annison, E. F. (1954). Some observations on volatile fatty acids in the sheep's rumen. Biochemical Journal 57, 400–5.CrossRefGoogle ScholarPubMed
Armstrong, D. G. & Annison, E. F. (1973). Amino acid requirements and amino acid supply in the sheep. Proceedings of the Nutrition Society 32, 107–13.CrossRefGoogle ScholarPubMed
Ashwell, G. (1957). Colorimetric analysis of sugars. In Methods in Enzymology, vol. III (ed. Colowick, S. P. and Kaplan, N. O.), p. 73. London: Academic Press.Google Scholar
Association of Official Agricultural Chemists (1965). Official Methods of Analysis, 10th ed.Washington: A.O.A.C.Google Scholar
Beever, D. E., Coelho da Silva, J. F., Prescott, J. H. D. & Armstrong, D. G. (1972). The effect in sheep of physical form and stage of growth on the sites of digestion of a dried grass. 1. Sites of digestion of organic matter, energy and carbohydrate. British Journal of Nutrition 28, 347–56.CrossRefGoogle ScholarPubMed
Beever, D. E., Thomson, D. J. & Harrison, D. G. (1971). The effects of drying and the comminution of red clover on its subsequent digestion by sheep. Proceedings of the Nutrition Society 30, 86–7 A.Google ScholarPubMed
Bidmead, D. S. & Ley, F. J. (1958). Quantitative amino acid analysis of food proteins by means of a single ion-exchange column. Biochimica et Biophysica Acta 29, 562–7.CrossRefGoogle ScholarPubMed
Bond, J. & Rumsey, T. S. (1973). Liquid molasses–urea or biuret (NPN) food supplements for beef cattle; wintering performance, ruminal differences and feeding patterns. Journal of Animal Science 37, 593–8.CrossRefGoogle Scholar
Broster, W. H. & Oldham, J. D. (1977). Protein quantity and quality for the UK dairy cow. In Nutrition and the Climatic Environment (ed. Haresign, W., Swan, H. and Lewis, D.), pp. 123–54. London: Butterworths.Google Scholar
Chamberlain, D. G., Thomas, P. C. & Wilson, A. G. (1976). Efficiency of bacterial protein synthesis in the rumen of sheep receiving a diet of sugar beet pulp and barley. Journal of the Science of Food and Agriculture 27, 231–8.CrossRefGoogle ScholarPubMed
Clarke, J., Geerken, C. M., Preston, T. R. & Zamora, A. (1973). Molasses as an energy source in low fibre diets for milk production. 3. The effect of varying the molasses: grain ratio in a low fibre basal diet. Cuban Journal of Agricultural Science 7, 155–67.Google Scholar
Clarke, E. M. W., Ellinger, G. M. & Phillipson, A. T. (1966). The influence of diet on the nitrogenous components passing to the duodenum and through the lower ileum of sheep. Proceedings of the Royal Society B 166, 6379.Google Scholar
Conway, E. J. (1957). Microdiffusion Analysis and Volumetric Error, 4th ed.London: Crosby Lockwood.Google Scholar
Eadie, J. M., Hyldgaard-Jensen, J., Mann, S. O., Reid, R. S. & Whitelaw, F. G. (1970). Observations on the microbiology and biochemistry of the rumen in cattle given different quantities of a pelleted barley ration. British Journal of Nutrition 24, 157–77.CrossRefGoogle ScholarPubMed
Erwin, E. S., Marco, G. J. & Emery, E. M. (1961). Volatile fatty acid analyses of blood and rumen fluid by gas chromatography. Journal of Dairy Science 44, 1768–71.CrossRefGoogle Scholar
Harrop, C. J. F. (1974). Nitrogen metabolism in the ovine stomach. 4. Nitrogenous components of the abomasal secretions. Journal of Agricultural Science, Cambridge 83, 249–57.CrossRefGoogle Scholar
Hatch, C. F. & Beeson, W. M. (1972). Effect of different levels of cane molasses on nitrogen and energy utilisation in urea rations for steers. Journal of Animal Science 35, 854–8.CrossRefGoogle ScholarPubMed
Ishaque, M., Rook, J. A. F. & Thomas, P. C. (1971). Relationship between the pattern of ruminal fermentation and the flow of materials to the duodenum in sheep receiving a diet of barley, flaked maize and ground hay. Proceedings of the Nutrition Society 30, 12 A.Google Scholar
Jackson, P., Rook, J. A. F. & Towers, K. G. (1971). The physical form of a barley grain and barley straw diet and nitrogen metabolism in sheep. Proceedings of the Nutrition Society 30, 1A.Google ScholarPubMed
Jollés, P. (1967). Relationship between chemical structure and biological activity of hen egg-white lysozyme and lysozymes of different species. Proceedings of the Royal Society B 167, 350–64.Google ScholarPubMed
Kempthorne, P. (1952). The Design and Analysis of Experiments. New York: Wiley.CrossRefGoogle Scholar
Koval, M. P. (1974). (Effect of urea and readily fermentable carbohydrates on nitrogen metabolism in fattening bullocks.) Khimiya v Sel'skom Khozyaistve 12, 866–7 (through Nutrition Abstracts and Reviews (1975) 45, 1057).Google Scholar
Leibholz, J. & Hartmann, P. E. (1972). Nitrogen metabolism in sheep. 1. The effect of protein and energy intake on the flow of digesta into the duodenum and on the digestion and absorption of nutrients. Australian Journal of Agricultural Research 23, 1059–72.CrossRefGoogle Scholar
Leng, R. A. & Preston, T. R. (1976). Sugar cane for cattle production. Present constraints, perspectives and research priorities. Tropical Animal Production 1, 122.Google Scholar
Lewis, D., Hill, K. J. & Annison, E. F. (1957). Studies on the portal blood of sheep. I. Absorption of ammonia from the rumen of the sheep. Biochemical Journal 66, 587–92.CrossRefGoogle ScholarPubMed
Ling, J. R. (1976). Nitrogen metabolism in the rumen. Ph.D. thesis University of Nottingham.Google Scholar
Marty, R. J. & Preston, T. R. (1970). Molar proportions of short-chain volatile fatty acids (VFA) produced in the rumen of cattle given high-molasses diets. Revista Cubana de Ciencia Agricola 4, 183–6.Google Scholar
Miller, E. L. (1973). Evaluation of foods as sources of nitrogen and amino acids. Proceedings of the Nutrition Society 32, 7984.CrossRefGoogle ScholarPubMed
Moore, S. (1963). On the determination of cystine as cysteic acid Journal of Biological Chemistry 238, 235–7.CrossRefGoogle Scholar
Nicholson, J. W. E. & Sutton, J. D. (1969). The effect of diet composition and level of feeding on digestion in the stomach and intestines of sheep. British Journal of Nutrition 23, 585–91.CrossRefGoogle ScholarPubMed
Nolan, J. V. & Leng, R. A. (1972). Dynamic aspects of ammonia and urea metabolism in sheep. British Journal of Nutrition 27, 177–94.CrossRefGoogle ScholarPubMed
Oldham, J. D. & Ling, J. R. (1977). Measurement of the rate of flow of digesta passing through the duodenum of sheep. British Journal of Nutrition 37, 333–43.CrossRefGoogle ScholarPubMed
Ørskov, E. R., Fraser, C. & McDonald, I. (1971). Digestion of concentrates in sheep. 2. The effect of urea or fishmeal supplementation of barley diets on the apparent digestion of protein, fat, starch and ash in the rumen, the small intestine and the large intestine, and calculation of volatile fatty acid production. British Journal of Nutrition 25, 243–62.CrossRefGoogle Scholar
Satter, L. D. & Slyter, L. L. (1974). Effect of ammonia concentration on rumen microbial protein production in vitro. British Journal of Nutrition 32, 199208.CrossRefGoogle ScholarPubMed
Sutton, J. D. (1968). The fermentation of soluble carbohydrates in rumen contents of cows fed diets containing a large proportion of hay. British Journal of Nutrition 22, 689712.CrossRefGoogle ScholarPubMed
Sutton, J. D. (1969), The fermentation of soluble carbohydrates in rumen contents of cows given diets containing a large proportion of flaked maize. British Journal of Nutrition 23, 567–83.CrossRefGoogle ScholarPubMed
Thompson, F. & Lamming, G. E. (1972). The flow of digesta, dry matter and starch to the duodenum in sheep given rations containing straw of variable particle size. British Journal of Nutrition 28, 391403.CrossRefGoogle Scholar
Thomson, D. J., Beever, D. E., Coelho da Silva, J. F. & Armstrong, D. G. (1972). The effect in sheep of physical form on the sites of digestion of a dried lucerne diet. 1. Sites of organic matter, energy and carbohydrate digestion. British Journal of Nutrition 28, 3141.CrossRefGoogle ScholarPubMed
Wakeling, A. E. (1970). The amino acid requirements of ruminants. Ph.D. thesis, University of Nottingham.Google Scholar
Weller, R. A. & Pilgrim, A. F. (1974). Passage of protozoa and volatile fatty acids from the rumen of the sheep and from a continuous in vitro fermentation system. British Journal of Nutrition 32, 341–51.CrossRefGoogle ScholarPubMed
Whitelaw, F. G., Eadie, J. M., Mann, S. O. & Reid, R. S. (1972). Some effects of rumen ciliate protozoa in cattle given restricted amounts of a barley diet. British Journal of Nutrition 27, 425–37.CrossRefGoogle ScholarPubMed