Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity

Lysozyme obtained from PC2 hyperimmune egg whites, originating from hens immunized with a complex of bacterial and fungal antigens, was purified by ion exchange chromatography on Amberlite FPC 3500 resin. The purity of lysozyme was analysed by polyacrylamide gel electrophoresis in denaturing system...

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Main Authors: Viorica Chiurciu, Teodora Supeanu, Ioana Alina Dimulescu, Cristina Urducea, Lucica Sima, Victoras I. Iordanescu, Mariana Oporanu
Format: Article
Language:English
Published: Romanian National Association of the Veterinary Products Manufacturers 2020-06-01
Series:Medicamentul Veterinar
Subjects:
Online Access:http://www.veterinarypharmacon.com/docs/2187-2020_VD_14(1)_ART_8_ENG.pdf
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spelling doaj-e649a3de71484cefbc683278545d0b772021-06-02T12:55:04ZengRomanian National Association of the Veterinary Products ManufacturersMedicamentul Veterinar1843-95272069-24632020-06-011418693Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activityViorica Chiurciu 0Teodora Supeanu1Ioana Alina Dimulescu2Cristina Urducea3Lucica Sima4Victoras I. Iordanescu5Mariana Oporanu6Romvac Company S.A. RomaniaRomvac Company S.A. RomaniaRomvac Company S.A. RomaniaRomvac Company S.A. RomaniaRomvac S.A. RomaniaRomvac Company S.A. RomaniaRomvac Company S.A. RomaniaLysozyme obtained from PC2 hyperimmune egg whites, originating from hens immunized with a complex of bacterial and fungal antigens, was purified by ion exchange chromatography on Amberlite FPC 3500 resin. The purity of lysozyme was analysed by polyacrylamide gel electrophoresis in denaturing system (SDS-PAGE). Based on the migration pattern of the molecular marker, the presence of a single band with a molecular mass of 14.1 kDa was found. The agar gel immunodiffusion test (AGID) showed the presence of lysozyme which was tested in dilutions from 1/2 to 1/32 as compared to standard lysozyme (Sigma) and that obtained from eggs from chickens free of specific germs (SPF) and conventional (CV). The immunological identity between the standard lysozyme and the PC2 lysozyme was established by the AGID test. The PC2 lysozyme showed agglutination reactions with flaky clumps in the presence of Micrococcus lysodeikticus cultures and with granular clumps in the presence of Staphylococcus aureus cultures. The antimicrobial activity of lysozyme was intense against Gram-positive bacteria and less intense against Gram-negatives. The concentration of lysozyme was assessed by the lysoplate method against a Micrococcus lysodeikticus culture. Mean values (x̄ ± ds) of purified lysozyme were obtained, ranging between 12.5 mg/mL and 14,0 mg/mL. Lythic units (mg/mL) were determined in immunologically active products containing lysozyme (gels, emulsions, solutions, powders). The mean values (x̄ ± ds) were between 49.0±0.34 and 60.5±0.84. This study suggests that PC2 lysozyme exhibits an immunologic activity with an important role in the mechanisms of non-specific defense of organisms. http://www.veterinarypharmacon.com/docs/2187-2020_VD_14(1)_ART_8_ENG.pdflysozymepurificationion exchange chromatographyamberlite fpc 3500micrococcus lysodeikticuslysoplate method
collection DOAJ
language English
format Article
sources DOAJ
author Viorica Chiurciu
Teodora Supeanu
Ioana Alina Dimulescu
Cristina Urducea
Lucica Sima
Victoras I. Iordanescu
Mariana Oporanu
spellingShingle Viorica Chiurciu
Teodora Supeanu
Ioana Alina Dimulescu
Cristina Urducea
Lucica Sima
Victoras I. Iordanescu
Mariana Oporanu
Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity
Medicamentul Veterinar
lysozyme
purification
ion exchange chromatography
amberlite fpc 3500
micrococcus lysodeikticus
lysoplate method
author_facet Viorica Chiurciu
Teodora Supeanu
Ioana Alina Dimulescu
Cristina Urducea
Lucica Sima
Victoras I. Iordanescu
Mariana Oporanu
author_sort Viorica Chiurciu
title Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity
title_short Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity
title_full Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity
title_fullStr Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity
title_full_unstemmed Lysozyme – bioactive component of the hyperimmune egg PC2: characterization, purification and antimicrobial activity
title_sort lysozyme – bioactive component of the hyperimmune egg pc2: characterization, purification and antimicrobial activity
publisher Romanian National Association of the Veterinary Products Manufacturers
series Medicamentul Veterinar
issn 1843-9527
2069-2463
publishDate 2020-06-01
description Lysozyme obtained from PC2 hyperimmune egg whites, originating from hens immunized with a complex of bacterial and fungal antigens, was purified by ion exchange chromatography on Amberlite FPC 3500 resin. The purity of lysozyme was analysed by polyacrylamide gel electrophoresis in denaturing system (SDS-PAGE). Based on the migration pattern of the molecular marker, the presence of a single band with a molecular mass of 14.1 kDa was found. The agar gel immunodiffusion test (AGID) showed the presence of lysozyme which was tested in dilutions from 1/2 to 1/32 as compared to standard lysozyme (Sigma) and that obtained from eggs from chickens free of specific germs (SPF) and conventional (CV). The immunological identity between the standard lysozyme and the PC2 lysozyme was established by the AGID test. The PC2 lysozyme showed agglutination reactions with flaky clumps in the presence of Micrococcus lysodeikticus cultures and with granular clumps in the presence of Staphylococcus aureus cultures. The antimicrobial activity of lysozyme was intense against Gram-positive bacteria and less intense against Gram-negatives. The concentration of lysozyme was assessed by the lysoplate method against a Micrococcus lysodeikticus culture. Mean values (x̄ ± ds) of purified lysozyme were obtained, ranging between 12.5 mg/mL and 14,0 mg/mL. Lythic units (mg/mL) were determined in immunologically active products containing lysozyme (gels, emulsions, solutions, powders). The mean values (x̄ ± ds) were between 49.0±0.34 and 60.5±0.84. This study suggests that PC2 lysozyme exhibits an immunologic activity with an important role in the mechanisms of non-specific defense of organisms.
topic lysozyme
purification
ion exchange chromatography
amberlite fpc 3500
micrococcus lysodeikticus
lysoplate method
url http://www.veterinarypharmacon.com/docs/2187-2020_VD_14(1)_ART_8_ENG.pdf
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