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Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture
BACKGROUND AND OBJECTIVES: Cell-immobilization is used to maintain microbial culture to produce metabolites in repeated-batch or continuous fermentations, thereby reducing the time and resources spent on delivering mass production of microbe. The technique also enables shortening of the detoxificati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867643/ https://www.ncbi.nlm.nih.gov/pubmed/36721513 http://dx.doi.org/10.18502/ijm.v14i4.10236 |
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author | Rakhshandeh, Hakimeh Shamsaddini Bafti, Mehrdad Familsatarian, Behnaz Nooshadokht, Maryam Khazaeli, Payam Raiesi, Omid Amirheidari, Bagher |
author_facet | Rakhshandeh, Hakimeh Shamsaddini Bafti, Mehrdad Familsatarian, Behnaz Nooshadokht, Maryam Khazaeli, Payam Raiesi, Omid Amirheidari, Bagher |
author_sort | Rakhshandeh, Hakimeh |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Cell-immobilization is used to maintain microbial culture to produce metabolites in repeated-batch or continuous fermentations, thereby reducing the time and resources spent on delivering mass production of microbe. The technique also enables shortening of the detoxification phase and the amount of formaldehyde required due to low incidence of viable bacteria in the extract. MATERIALS AND METHODS: A solution of sodium alginate containing Clostridium perfringens cells was dropped into stirring CaCl solution via a sterile syringe needle. Optimizations resulted in reasonably uniform beads containing C. perfringens. Beads were externally stabilized by poly L-lysine, followed by immersion in a solution of Na-alginate to coat them with a new layer of alginate forming an alginate-PLL-alginate cortex. RESULTS: This study proved successful in immobilizing C. perfringens cells inside uniform alginate microspheres. Cell loading and cell propagation inside the beads were measured. The cell loaded beads were cultivable in liquid media producing 550 minimum lethal doses per milliliter (MLD/ml) in a 72 h. CONCLUSION: The research paved the way for further investigations to optimize and establish an efficient bacterial encapsulation method. Thus, it seems possible to produce toxins from beads engulfing C. perfringens on larger scales via repeated-batch or continuous fermentation processes. |
format | Online Article Text |
id | pubmed-9867643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-98676432023-01-30 Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture Rakhshandeh, Hakimeh Shamsaddini Bafti, Mehrdad Familsatarian, Behnaz Nooshadokht, Maryam Khazaeli, Payam Raiesi, Omid Amirheidari, Bagher Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Cell-immobilization is used to maintain microbial culture to produce metabolites in repeated-batch or continuous fermentations, thereby reducing the time and resources spent on delivering mass production of microbe. The technique also enables shortening of the detoxification phase and the amount of formaldehyde required due to low incidence of viable bacteria in the extract. MATERIALS AND METHODS: A solution of sodium alginate containing Clostridium perfringens cells was dropped into stirring CaCl solution via a sterile syringe needle. Optimizations resulted in reasonably uniform beads containing C. perfringens. Beads were externally stabilized by poly L-lysine, followed by immersion in a solution of Na-alginate to coat them with a new layer of alginate forming an alginate-PLL-alginate cortex. RESULTS: This study proved successful in immobilizing C. perfringens cells inside uniform alginate microspheres. Cell loading and cell propagation inside the beads were measured. The cell loaded beads were cultivable in liquid media producing 550 minimum lethal doses per milliliter (MLD/ml) in a 72 h. CONCLUSION: The research paved the way for further investigations to optimize and establish an efficient bacterial encapsulation method. Thus, it seems possible to produce toxins from beads engulfing C. perfringens on larger scales via repeated-batch or continuous fermentation processes. Tehran University of Medical Sciences 2022-08 /pmc/articles/PMC9867643/ /pubmed/36721513 http://dx.doi.org/10.18502/ijm.v14i4.10236 Text en Copyright © 2022 The Authors. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Rakhshandeh, Hakimeh Shamsaddini Bafti, Mehrdad Familsatarian, Behnaz Nooshadokht, Maryam Khazaeli, Payam Raiesi, Omid Amirheidari, Bagher Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture |
title | Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture |
title_full | Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture |
title_fullStr | Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture |
title_full_unstemmed | Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture |
title_short | Immobilization of Clostridium perfringens type D in calcium alginate beads: toxin production mimics free cell culture |
title_sort | immobilization of clostridium perfringens type d in calcium alginate beads: toxin production mimics free cell culture |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867643/ https://www.ncbi.nlm.nih.gov/pubmed/36721513 http://dx.doi.org/10.18502/ijm.v14i4.10236 |
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