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Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches

Herein, enhancements of the yield and antimicrobial activity duration of the bacteriocin avicin A were accomplished using fractional factorial design (FFD) and layered double hydroxide (LDH) nanoparticles. Firstly, potential factors affecting bacteriocin production were selected for preliminary stud...

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Autores principales: Fahim, Hazem A., Rouby, Waleed M. A. El, El-Gendy, Ahmed O., Khairalla, Ahmed S., Naguib, Ibrahim A., Farghali, Ahmed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587769/
https://www.ncbi.nlm.nih.gov/pubmed/28878272
http://dx.doi.org/10.1038/s41598-017-10157-9
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author Fahim, Hazem A.
Rouby, Waleed M. A. El
El-Gendy, Ahmed O.
Khairalla, Ahmed S.
Naguib, Ibrahim A.
Farghali, Ahmed A.
author_facet Fahim, Hazem A.
Rouby, Waleed M. A. El
El-Gendy, Ahmed O.
Khairalla, Ahmed S.
Naguib, Ibrahim A.
Farghali, Ahmed A.
author_sort Fahim, Hazem A.
collection PubMed
description Herein, enhancements of the yield and antimicrobial activity duration of the bacteriocin avicin A were accomplished using fractional factorial design (FFD) and layered double hydroxide (LDH) nanoparticles. Firstly, potential factors affecting bacteriocin production were selected for preliminary study. By a 2(5-1) FFD, high pH was shown to have a positive effect on avicin A yield, while temperature and duration of incubation, as well as peptone nitrogen sources all had negative effects. The highest bacteriocin production and activity (2560 BU/ml) were observed after 30 h of incubation at 30 °C, with pH adjustment at 7, and in the presence of 2 g mannitol as carbon source and 2.2 g peptone as nitrogen source. Secondly, avicin A nanocomposites with different LDH precursors were tested. Only avicin A-ZnAl-CO(3) LDH demonstrated a potent antimicrobial activity against Lactobacillus sakei LMGT 2313 that lasted for at least 24 days, as compared to the values of 6 and 15 days observed with the free avicin A that has been stored at room temperature and at 4 °C, respectively. In conclusion, avicin A production and stability can be improved by manipulating the growth conditions and media composition, together with conjugation to LDHs.
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spelling pubmed-55877692017-09-13 Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches Fahim, Hazem A. Rouby, Waleed M. A. El El-Gendy, Ahmed O. Khairalla, Ahmed S. Naguib, Ibrahim A. Farghali, Ahmed A. Sci Rep Article Herein, enhancements of the yield and antimicrobial activity duration of the bacteriocin avicin A were accomplished using fractional factorial design (FFD) and layered double hydroxide (LDH) nanoparticles. Firstly, potential factors affecting bacteriocin production were selected for preliminary study. By a 2(5-1) FFD, high pH was shown to have a positive effect on avicin A yield, while temperature and duration of incubation, as well as peptone nitrogen sources all had negative effects. The highest bacteriocin production and activity (2560 BU/ml) were observed after 30 h of incubation at 30 °C, with pH adjustment at 7, and in the presence of 2 g mannitol as carbon source and 2.2 g peptone as nitrogen source. Secondly, avicin A nanocomposites with different LDH precursors were tested. Only avicin A-ZnAl-CO(3) LDH demonstrated a potent antimicrobial activity against Lactobacillus sakei LMGT 2313 that lasted for at least 24 days, as compared to the values of 6 and 15 days observed with the free avicin A that has been stored at room temperature and at 4 °C, respectively. In conclusion, avicin A production and stability can be improved by manipulating the growth conditions and media composition, together with conjugation to LDHs. Nature Publishing Group UK 2017-09-06 /pmc/articles/PMC5587769/ /pubmed/28878272 http://dx.doi.org/10.1038/s41598-017-10157-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fahim, Hazem A.
Rouby, Waleed M. A. El
El-Gendy, Ahmed O.
Khairalla, Ahmed S.
Naguib, Ibrahim A.
Farghali, Ahmed A.
Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches
title Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches
title_full Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches
title_fullStr Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches
title_full_unstemmed Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches
title_short Enhancement of the productivity of the potent bacteriocin avicin A and improvement of its stability using nanotechnology approaches
title_sort enhancement of the productivity of the potent bacteriocin avicin a and improvement of its stability using nanotechnology approaches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587769/
https://www.ncbi.nlm.nih.gov/pubmed/28878272
http://dx.doi.org/10.1038/s41598-017-10157-9
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