You are here

Influence of soybean oil and fermented algae soluble lipid complex on productivity and quality of laying hen eggs

The studies examined the effects of soybean oil and various doses of a watersoluble lipid complex in a standard diet consisting of corn, soybean meal, sunflower meal, wheat germ and bran, limestone, monocalcium phosphate, table salt, baking soda, L-lysine, choline chloride, DL-methionine, L-threonine, adsorbent, and a vitamin and mineral mixture. During the experiment, egg productivity, feed consumption, live weight, physiological condition and safety of the controlled livestock were monitored. The eggs obtained during the experiment were weighed, morphometric indicators were determined (egg mass, mass of albumen, yolk, shell and its thickness and strength, shape index, viscosity coefficient, pH of albumen and yolk, refractive index). The content of total lipids and vitamins A and E was determined in the egg yolk. As a result of the research, it was found that the egg-laying process in all experimental groups began at 115 days and at 140 days of age the productivity was 39,50–42,35 %. The peak of egg productivity occurred at 200 days and was 95,30–96,80 % and was maintained at a high level until 320 days of age (94,50–95,75 %). On average, for the entire period of the experiment, which lasted until the age of 450 days, egg production was 84,23–85,79 %. The highest productivity was in the III experimental group, which received 1,0–1,3 % of the fermented water-soluble lipid complex. Morphometric indicators of eggs in all experimental groups were approximately at the unit level and were within the normal range. At the age of the most intensive egg laying, the mass of eggs was 60,15–61,85 g. The highest mass of eggs was in the III and IV groups, which received 1,0–1,6 % of the fermented watersoluble lipid complex. During the experimental period, 15,97–17,09 kg of egg mass per head was obtained from laying hens. The content of total lipids, vitamins A and E was higher in the III experimental group, by 8,10; 5,81 and 10,71 %, respectively. The live weight of laying hens corresponded to the recommendations for keeping laying hens Loman LSL-classic. Therefore, adding a fermented water-soluble lipid complex instead of soybean oil is appropriate and economically beneficial, since its cost is 24 % lower.

Keywords: laying hens, egg production, morphometric indicators, soybean oil, water-soluble lipid complex, egg yolk, total lipids, vitamins A, E.

  1. Wang, J., Chi, Y., Cheng, Y., Zhao, Y. (2018). Physicochemical properties, in vitro digestibility and antioxidant activity of dry-heated egg white protein. Food Chemistry, 246, pp. 18–25.
  2. Hida, A., Hasegawa, Y., Mekata, Y., Usuda, M., Masuda, Y., Kawano, H. (2012). Effects of egg white protein supplementation on muscle strength and serum free amino acid concentrations. Nutrients, 4 (10), pp. 1504–1517.
  3. Evenepoel, P., Geypens, B., Luypaerts, A., Hiele, M., Ghoos, Y., Rutgeerts, P. (1998). Digestibility of cooked and raw egg protein in humans as assessed by stable isotope techniques. Journal of Nutrition, 128 (10), pp. 1716–1722.
  4. Siddik, M.A.B., Moghaddam, M.Z., Hegde, V., Shin, A. (2019). Branched-chain amino acid metabolism is impaired in mice and humans with Alzheimer's disease (OR27-04-19). Current Develop ments in Nutrition, 3.
  5. Marchesini, G., Marzocchi, R., Noia, M., Bianchi, G. (2005). Branched-chain amino acid supplementation in patients with liver diseases. Journal of Nutrition, 135 (6), pp. 1596–1601.
  6. Molema, F., Gleich, F., Burgard, P., van der Ploeg, A.T., Summar, M.L., Chapman, K.A. (2019). Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branchedchain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment. Molecular Genetics and Metabolism, 126 (4), pp. 397–405.
  7. Holeček, M. (2018). Branched-chain amino acids in health and disease: Metabolism, alterations in blood plasma, and as supplements. Nutrition & Metabolism, 15 (1), 33 p.
  8. Dasarathy, S., Hatzoglou, M.B. (2018). Hyperammonemia and proteostasis in cirrhosis. Current Opinion in Clinical Nutrition and Metabolic Care. 21 (1), 30 p.
  9. Kulyk M.F., Kravtsiv R.Y., Obertyukh Yu.V. (2003). Feed, evaluation, use of livestock products, ecology: a guide. Vinnytsia: PP Publishing House "Tezis", 334 p. (In Ukrainian).
  10. Zhu, Y., Vanga, S.K., Wang, J., Raghavan, V. (2018). Impact of food processing on the structural and allergenic properties of egg white. Trends in Food Science & Technology, 78, pp. 188–196.
  11. Farjami, T., Madadlou, A., Labbafi, M. (2016). Modulating the textural characteristics of whey protein nanofibril gels with different concentra tions of calcium chloride. Journal of Dairy Research, 83 (1), pp. 109–114.
  12. Ibatulin, I.I., Chygrin, A.I. (2013). 2013: Workshop on feeding farm animals: textbook. Zhytomyr: «Polissya», 441 p. (In Ukrainian).
  13. Selvaraj, R.K., Cherian, G. (2004). Dietary n-3 fatty acids reduce the delayed hypersensitivity reaction and antibody production more than n-6 fatty acids in broiler birds. Eur. J. Lipid Sci. Technol., 106 (1), pp. 3–10.
  14. Laye, S., Nadjar, A., Joffre, C., Bazinet, R.P. (2018). Anti-infl ammatory effects of omega-3 fatty acids in the brain: physiological mechanisms and relevance to pharmacology. Pharmacol. Rev., 70 (1), pp. 12–38.
  15. Yang, X., Guo, Y., He, X., Yuan, J., Yang, Y., Wang, Z. (2008). Growth performance and immune responses in chickens after challenge with lipopolysaccharide and modulation by dietary different oils. Animal, 2 (2), pp. 216–223.
  16. Lawlor, J.B., Gaudette, N., Dickson, T., House, J.D. (2010). Fatty acid profile and sensory characteristics of table eggs from laying hens fed diets containing microencapsulated fish oil. Anim. Feed Sci. Technol., 156 (3–4), pp. 97–103.
  17. Carragher, J.F., Muhlhausler, B.S., Geier, M.S., House, J.D., Hughes, R.J., Gibson, R.A. (2016). Effect of dietary ALA on growth rate, feed conversion ratio, mortality rate and breast meat omega-3 LCP- UFA content in broiler chickens. Anim. Prod. Sci., 56 (5), pp. 815–823.
  18. Sijben, J.W., Klasing, K.C., Schrama, J.W., Parmentier, H.K., van der Poel, J.J., Savelkoul, H.F. (2003). Early in vivo cytokine genes expression in chickens after challenge with Salmonella typhimurium lipopolysaccharide and modulation by dietary n--3 polyunsaturated fatty acids. Dev. Comp. Immunol., 27 (6–7), pp. 611–619.
  19. Ding, X., Yu, Y., Su, Z., Zhang, K. (2017). Effects of essential oils on performance, egg quality, nutrient digestibility and yolk fatty acid profile in laying hens. Anim. Nutr., 3, pp. 127–131. PubMed
  20. Vakili, R., Majidzadeh Heravi, R. (2016). Performance and egg quality of laying hens fed diets supplemented with herbal extracts and flaxseed. Poult. Sci. J., 4, pp. 107–116.
  21. Ding, X., Yu, Y., Su, Z., Zhang, K. (2017). Effects of essential oils on performance, egg quality, nutrient digestibility and yolk fatty acid profile in laying hens. Anim. Nutr., 3, pp. 127–131. PubMed
  22. Bontempo V., Comi M., Jiang X.R., Rebucci R., Caprarulo V., Giromini C., Gottardo D., Fusi E., Stella S., Tirloni E., Cattaneo D., Baldi, A. (2018). Evaluation of a synthetic emulsifier product supplementation on broiler chicks. Anim. Feed Sci. Technol., 240, pp. 157–164.
  23. Boontiam, W., Hyun, Y.K., Jung, B.,  Kim, Y.Y. (2019). Effects of lysophospholipid supplementation to reduced energy, crude protein, and amino acid diets on growth performance, nutrient digestibility, and blood profiles in broiler chickens. Poult. Sci., 98, pp. 6693–6701. DOI:10.3382/ps/pex005.
  24. Boontiam, W., Jung, B., Kim, Y.Y. (2017). Effects of lysophospholipid supplementation to lower nutrient diets on growth performance, intestinal morphology, and blood metabolites in broiler chickens. Poult. Sci., 96, pp. 593–601. DOI:10.3382/ps/pew269.
  25. Farjami, T., Babaei, J., Nau, F., Dupont, D., Madadlou, A. (2021). Effects of thermal, non-thermal and emulsifi cation processes on the gastrointestinal digestibility of egg white proteins. Trends Food Sci. Technol., 107, pp. 45–56.
  26. Haetinger, V.S., Dalmoro, Y.K., Godoy, G.L., Lang, M.B., de Souza, O.F., Aristimunha, P., Stefanello, C. (2021). Optimizing cost, growth performance, and nutrient absorption with a bio-emulsifier based on lysophospholipids for broiler chickens. Poult. Sci., 100. DOI:10.1016/j.psj.2021.101025.
  27. Zhao, P.Y., Kim, I.H. (2017). Effect of diets with different energy and lysophospholipids levels on performance, nutrient metabolism, and body composition in broilers. Poult. Sci., 96. pp. 1341–1347. DOI:10.3382/ps/pew469.
  28. Kyryliv, Ya.I., Ratych, I.B. (2003). Quality assessment of compound feeds for poultry and poultry products. Lviv, 241p. (In Ukrainian).
  29. Vlizlo, V.V., Fedoruk, R.S., Ratych, I.B. (2012). Laboratory research methods in biology, animal husbandry and veterinary medicine: a reference book. Lviv: SPOLOM, 764 p. (In Ukrainian).
  30. Neijat, M., Suh, M., Neufeld, J., House, J.D. (2016). Increasing levels of dietary hempseed products leads to differential responses in the fatty acid profiles of egg yolk, liver and plasma of laying hens. Lipids, 51 (5), pp. 615–633.
  31. Neijat, M., Ojekudo, O., House, J.D. (2016). Effect of flaxseed oil and microalgae DHA on the production performance, fatty acids and total lipids of egg yolk and plasma in laying hens. Prostaglandins Leukot. Essent. Fatty Acids., 115, pp. 77–88.
  32. Neijat, M., Eck, P., House, J.D. (2017). Impact of dietary precursor ALA versus preformed DHA on fatty acid profi les of eggs, liver and adipose tissue and expression of genes associated with hepatic lipid metabolism in laying hens. Prostaglandins Leukot. Essent. Fatty Acids., 119, pp. 1–17.
  33. Fraeye, I., Bruneel, C., Lemahieu, C., Buyse, J., Muylaert, K., Foubert, I. (2012). Dietary enrichment of eggs with omega-3 fatty acids: a review. Food Res. Int., 48 (2), pp. 961–969.
  34. Hall, J.A., Jha, S., Skinner, M.M., Cherian, G. (2007). Maternal dietary n-3 fatty acids alter immune cell fatty acid composition and leukotriene production in growing chicks. Prostaglandins Leukot. Essent. Fatty Acids., 76 (1), pp. 19–28.
  35. Mousavi, A., Mahdavi, A.H., Riasi, A., Soltani-Ghombavani, M. (2017). Synergetic effects of essential oils mixture improved egg quality traits, oxidative stability and liver health indices in laying hens fed fi sh oil. Anim. Feed Sci. Technol., 234, pp. 162–172.
  36. Zivkovic, A.M., Telis, N., German, J.B., Hammock, B.D. (2011). Dietary omega-3 fatty acids aid in the modulation of infl ammation and metabolic health. Calif. Agric. (Berkeley), 65 (3), 106 p.
  37. Eilati, 1.1.1.E., Small, C.C., McGee, S.R., Kurrey, N.K., Hales, D.B. (2013). Anti-inflammatory effects of fish oil in ovaries of laying hens target pros taglandin pathways. Lipids Health Dis, 12 (1), 152 p.
  38. Eilati, E., Bahr, J.M., Hales, D.B. (2013). Long term consumption of flaxseed enriched diet decreased ovarian cancer incidence and prostaglandin E2 in hens. Gynecol. Oncol., 130 (3), pp. 620–628.
  39. Gakhar, N., Goldberg, E., Jing, M., Gibson, R., House, J.D. (2012). Effect of feeding hemp seed and hemp seed oil on laying hen performance and egg yolk fatty acid content: evidence of their safety and efficacy for laying hen diets. Poult. Sci., 91 (3), pp. 701–711.
  40. Cachaldora, P., Garcia-Rebollar, P., Alvarez, C., De Blas, J.C., Mendez, J. (2006). Effect of type and level of fish oil supplementation on yolk fat composition and n-3 fatty acids retention efficiency in laying hens. Br. Poult. Sci., 47 (1), pp. 43–49.
AttachmentSize
PDF icon protsaylo_1_2026_.pdf515.25 KB