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PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003

Among the different tools which can be studied and managed to tailor-make polyhydroxyalkanoates (PHAs) and enhance their production, bacterial strain and carbon substrates are essential. The assimilation of carbon sources is dependent on bacterial strain’s metabolism and consequently cannot be disso...

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Autores principales: Thomas, Tatiana, Sudesh, Kumar, Bazire, Alexis, Elain, Anne, Tan, Hua Tiang, Lim, Hui, Bruzaud, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175313/
https://www.ncbi.nlm.nih.gov/pubmed/32244900
http://dx.doi.org/10.3390/bioengineering7010029
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author Thomas, Tatiana
Sudesh, Kumar
Bazire, Alexis
Elain, Anne
Tan, Hua Tiang
Lim, Hui
Bruzaud, Stéphane
author_facet Thomas, Tatiana
Sudesh, Kumar
Bazire, Alexis
Elain, Anne
Tan, Hua Tiang
Lim, Hui
Bruzaud, Stéphane
author_sort Thomas, Tatiana
collection PubMed
description Among the different tools which can be studied and managed to tailor-make polyhydroxyalkanoates (PHAs) and enhance their production, bacterial strain and carbon substrates are essential. The assimilation of carbon sources is dependent on bacterial strain’s metabolism and consequently cannot be dissociated. Both must wisely be studied and well selected to ensure the highest production yield of PHAs. Halomonas sp. SF2003 is a marine bacterium already identified as a PHA-producing strain and especially of poly-3-hydroxybutyrate (P-3HB) and poly-3-hydroxybutyrate-co-3-hydroxyvalerate (P-3HB-co-3HV). Previous studies have identified different genes potentially involved in PHA production by Halomonas sp. SF2003, including two phaC genes with atypical characteristics, phaC1 and phaC2. At the same time, an interesting adaptability of the strain in front of various growth conditions was highlighted, making it a good candidate for biotechnological applications. To continue the characterization of Halomonas sp. SF2003, the screening of carbon substrates exploitable for PHA production was performed as well as production tests. Additionally, the functionality of both PHA synthases PhaC1 and PhaC2 was investigated, with an in silico study and the production of transformant strains, in order to confirm and to understand the role of each one on PHA production. The results of this study confirm the adaptability of the strain and its ability to exploit various carbon substrates, in pure or mixed form, for PHA production. Individual expression of PhaC1 and PhaC2 synthases in a non-PHA-producing strain, Cupriavidus necator H16 PHB¯4 (DSM 541), allows obtaining PHA production, demonstrating at the same time, functionality and differences between both PHA synthases. All the results of this study confirm the biotechnological interest in Halomonas sp. SF2003.
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spelling pubmed-71753132020-04-28 PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003 Thomas, Tatiana Sudesh, Kumar Bazire, Alexis Elain, Anne Tan, Hua Tiang Lim, Hui Bruzaud, Stéphane Bioengineering (Basel) Article Among the different tools which can be studied and managed to tailor-make polyhydroxyalkanoates (PHAs) and enhance their production, bacterial strain and carbon substrates are essential. The assimilation of carbon sources is dependent on bacterial strain’s metabolism and consequently cannot be dissociated. Both must wisely be studied and well selected to ensure the highest production yield of PHAs. Halomonas sp. SF2003 is a marine bacterium already identified as a PHA-producing strain and especially of poly-3-hydroxybutyrate (P-3HB) and poly-3-hydroxybutyrate-co-3-hydroxyvalerate (P-3HB-co-3HV). Previous studies have identified different genes potentially involved in PHA production by Halomonas sp. SF2003, including two phaC genes with atypical characteristics, phaC1 and phaC2. At the same time, an interesting adaptability of the strain in front of various growth conditions was highlighted, making it a good candidate for biotechnological applications. To continue the characterization of Halomonas sp. SF2003, the screening of carbon substrates exploitable for PHA production was performed as well as production tests. Additionally, the functionality of both PHA synthases PhaC1 and PhaC2 was investigated, with an in silico study and the production of transformant strains, in order to confirm and to understand the role of each one on PHA production. The results of this study confirm the adaptability of the strain and its ability to exploit various carbon substrates, in pure or mixed form, for PHA production. Individual expression of PhaC1 and PhaC2 synthases in a non-PHA-producing strain, Cupriavidus necator H16 PHB¯4 (DSM 541), allows obtaining PHA production, demonstrating at the same time, functionality and differences between both PHA synthases. All the results of this study confirm the biotechnological interest in Halomonas sp. SF2003. MDPI 2020-03-20 /pmc/articles/PMC7175313/ /pubmed/32244900 http://dx.doi.org/10.3390/bioengineering7010029 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Thomas, Tatiana
Sudesh, Kumar
Bazire, Alexis
Elain, Anne
Tan, Hua Tiang
Lim, Hui
Bruzaud, Stéphane
PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
title PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
title_full PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
title_fullStr PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
title_full_unstemmed PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
title_short PHA Production and PHA Synthases of the Halophilic Bacterium Halomonas sp. SF2003
title_sort pha production and pha synthases of the halophilic bacterium halomonas sp. sf2003
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175313/
https://www.ncbi.nlm.nih.gov/pubmed/32244900
http://dx.doi.org/10.3390/bioengineering7010029
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