Separation of ovotransferrin and ovomucoid from chicken egg white

• Published in: Poultry science Vol. 93; no. 4; pp. 1010 - 1017
• Main Authors: Abeyrathne, E D N S, Lee, H Y, Ahn, D U
• Format: Journal Article
• Language: English
• Published: England 01-04-2014
• Subjects: Animals; Blotting, Western; Chemical Precipitation; Chickens; Conalbumin - chemistry; Conalbumin - isolation & purification; Egg White - chemistry; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay; Ethanol - chemistry; Food Handling - economics; Food Handling - methods; Ovomucin - chemistry; Ovomucin - isolation & purification; acidic salt; ethanol precipitation; purity; ovomucoid; ovotransferrin; yield
• ISSN: 0032-5791
• DOI: 10.3382/ps.2013-03649

Ovotransferrin and ovomucoid were separated using 2 methods after extracting the ovotransferrin- and ovomucoid-containing fraction from egg white. Diluted egg white (2×) was added to Fe(3+) and treated with 43% ethanol (final concentration). After centrifugation, the supernatant was collected and treated with either a high-level ethanol (61% final concentration) or an acidic salt combination (2.5% ammonium sulfate and 2.5% citric acid) to separate ovotransferrin and ovomucoid. For the high-level of ethanol method, ovotransferrin was precipitated using 61% ethanol. After centrifugation, the precipitant was dissolved in 9 vol. of distilled water and the residual ethanol in the solution was removed using ultrafiltration. The supernatant, mainly containing ovomucoid, was diluted with 4 vol. of water, had ethanol removed, and was then concentrated and used as the ovomucoid fraction. For the acidic salt precipitation method, the ethanol in the supernatant was removed first. The ethanol-free solution was then concentrated and treated with a 2.5% ammonium sulfate and 2.5% citric acid combination. After centrifugation, the precipitant was used as the ovotransferrin and the supernatant as the ovomucoid fraction. The ovomucoid fraction from both of the protocols was further purified by heating at 65°C for 20 min and the impurities were removed by centrifugation. The yields of ovomucoid and ovotransferrin were >96 and >92%, respectively. The purity of ovomucoid was >89% and that of the ovotransferrin was >88%. The ELISA results confirmed that the activity of the separated ovotransferrin was >95%. Both of the protocols separated ovotransferrin and ovomucoid effectively and the methods were simple, fast, and easy to scale up.