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Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid

BACKGROUND: Hyaluronic acid, a natural polymer with wide applications in biomedicine and cosmetics, is mainly produced by Streptococcal fermentation at industrial scale. In the present study, chemical random mutagenesis was used for development of Streptococcus equisimilis group G mutant strains wit...

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Autores principales: Jafari, Bahareh, Keramati, Malihe, Ahangari Cohan, Reza, Atyabi, Seyed Mohammad, Hosseinzadeh, Sara Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute of Iran 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841222/
https://www.ncbi.nlm.nih.gov/pubmed/36437793
http://dx.doi.org/10.52547/ibj.3789
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author Jafari, Bahareh
Keramati, Malihe
Ahangari Cohan, Reza
Atyabi, Seyed Mohammad
Hosseinzadeh, Sara Ali
author_facet Jafari, Bahareh
Keramati, Malihe
Ahangari Cohan, Reza
Atyabi, Seyed Mohammad
Hosseinzadeh, Sara Ali
author_sort Jafari, Bahareh
collection PubMed
description BACKGROUND: Hyaluronic acid, a natural polymer with wide applications in biomedicine and cosmetics, is mainly produced by Streptococcal fermentation at industrial scale. In the present study, chemical random mutagenesis was used for development of Streptococcus equisimilis group G mutant strains with high HA productivity. METHODS: The optimum of the pH of culture condition and cultivation time for HA production by wild strain group G were assessed. At first, two rounds of mutation at different concentrations of NTG was used for mutagenesis. Then, the nonhemolytic and hyaluronidase-negative mutants were screened on the blood and HA agar. HA productivity and molecular weight were determined by carbazole assay, agarose gel electrophoresis and specific staining. Moreover, stability of the high producer mutants was evaluated within 10 generations. RESULTS: The results showed that the wild-type strain produced 1241 ± 2.1 µg/ml of HA at pH 5.5 and 4 hours of cultivation, while the screened mutants showed a 16.1-45.5% increase in HA production. Two mutant strains, named Gm2-120-21-3 (2470 ± 8.1 µg/ml) and Gm2-120-21-4 (2856 ± 4.2 µg/ml), indicated the highest titer and a consistent production. The Mw of HA for the mutants was less than 160 kDa, considering as a low Mw HA. CONCLUSION: The mutant strains producing a low polydisperse, as well as low Mw of HA with high titer might be regarded as potential industrial strains for HA production after further safety investigations.
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spelling pubmed-98412222023-01-24 Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid Jafari, Bahareh Keramati, Malihe Ahangari Cohan, Reza Atyabi, Seyed Mohammad Hosseinzadeh, Sara Ali Iran Biomed J Full Length BACKGROUND: Hyaluronic acid, a natural polymer with wide applications in biomedicine and cosmetics, is mainly produced by Streptococcal fermentation at industrial scale. In the present study, chemical random mutagenesis was used for development of Streptococcus equisimilis group G mutant strains with high HA productivity. METHODS: The optimum of the pH of culture condition and cultivation time for HA production by wild strain group G were assessed. At first, two rounds of mutation at different concentrations of NTG was used for mutagenesis. Then, the nonhemolytic and hyaluronidase-negative mutants were screened on the blood and HA agar. HA productivity and molecular weight were determined by carbazole assay, agarose gel electrophoresis and specific staining. Moreover, stability of the high producer mutants was evaluated within 10 generations. RESULTS: The results showed that the wild-type strain produced 1241 ± 2.1 µg/ml of HA at pH 5.5 and 4 hours of cultivation, while the screened mutants showed a 16.1-45.5% increase in HA production. Two mutant strains, named Gm2-120-21-3 (2470 ± 8.1 µg/ml) and Gm2-120-21-4 (2856 ± 4.2 µg/ml), indicated the highest titer and a consistent production. The Mw of HA for the mutants was less than 160 kDa, considering as a low Mw HA. CONCLUSION: The mutant strains producing a low polydisperse, as well as low Mw of HA with high titer might be regarded as potential industrial strains for HA production after further safety investigations. Pasteur Institute of Iran 2022-11 2022-10-30 /pmc/articles/PMC9841222/ /pubmed/36437793 http://dx.doi.org/10.52547/ibj.3789 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Length
Jafari, Bahareh
Keramati, Malihe
Ahangari Cohan, Reza
Atyabi, Seyed Mohammad
Hosseinzadeh, Sara Ali
Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid
title Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid
title_full Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid
title_fullStr Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid
title_full_unstemmed Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid
title_short Development of Streptococcus equisimilis Group G Mutant Strains with Ability to Produce Low Polydisperse and Low-Molecular-Weight Hyaluronic Acid
title_sort development of streptococcus equisimilis group g mutant strains with ability to produce low polydisperse and low-molecular-weight hyaluronic acid
topic Full Length
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841222/
https://www.ncbi.nlm.nih.gov/pubmed/36437793
http://dx.doi.org/10.52547/ibj.3789
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