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Cultivation technology development of Rhodothermus marinus DSM 16675

This work presents an evaluation of batch, fed-batch, and sequential batch cultivation techniques for production of R. marinus DSM 16675 and its exopolysaccharides (EPSs) and carotenoids in a bioreactor, using lysogeny broth (LB) and marine broth (MB), respectively, in both cases supplemented with 1...

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Autores principales: Ron, Emanuel Y. C., Sardari, Roya R. R., Anthony, Richard, van Niel, Ed W. J., Hreggvidsson, Gudmundur O., Nordberg-Karlsson, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801211/
https://www.ncbi.nlm.nih.gov/pubmed/31522265
http://dx.doi.org/10.1007/s00792-019-01129-0
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author Ron, Emanuel Y. C.
Sardari, Roya R. R.
Anthony, Richard
van Niel, Ed W. J.
Hreggvidsson, Gudmundur O.
Nordberg-Karlsson, Eva
author_facet Ron, Emanuel Y. C.
Sardari, Roya R. R.
Anthony, Richard
van Niel, Ed W. J.
Hreggvidsson, Gudmundur O.
Nordberg-Karlsson, Eva
author_sort Ron, Emanuel Y. C.
collection PubMed
description This work presents an evaluation of batch, fed-batch, and sequential batch cultivation techniques for production of R. marinus DSM 16675 and its exopolysaccharides (EPSs) and carotenoids in a bioreactor, using lysogeny broth (LB) and marine broth (MB), respectively, in both cases supplemented with 10 g/L maltose. Batch cultivation using LB supplemented with maltose (LB(malt)) resulted in higher cell density (OD(620) = 6.6) than use of MB(malt) (OD(620) = 1.7). Sequential batch cultivation increased the cell density threefold (OD(620) = 20) in LB(malt) and eightfold (OD(620) = 14) in MB(malt). In both single and sequential batches, the production of carotenoids and EPSs using LB(malt) was detected in the exponential phase and stationary phase, respectively, while in MB(malt) formation of both products was detectable in both the exponential and stationary phases of the culture. Heteropolymeric EPSs were produced with an overall volumetric productivity (Q(E)) of 0.67 (mg/L h) in MB(malt) and the polymer contained xylose. In LB, Q(E) was lower (0.1 mg/L h) and xylose could not be detected in the composition of the produced EPSs. In conclusion, this study showed the importance of a process design and medium source for production of R. marinus DSM 16675 and its metabolites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00792-019-01129-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-68012112019-11-01 Cultivation technology development of Rhodothermus marinus DSM 16675 Ron, Emanuel Y. C. Sardari, Roya R. R. Anthony, Richard van Niel, Ed W. J. Hreggvidsson, Gudmundur O. Nordberg-Karlsson, Eva Extremophiles Original Paper This work presents an evaluation of batch, fed-batch, and sequential batch cultivation techniques for production of R. marinus DSM 16675 and its exopolysaccharides (EPSs) and carotenoids in a bioreactor, using lysogeny broth (LB) and marine broth (MB), respectively, in both cases supplemented with 10 g/L maltose. Batch cultivation using LB supplemented with maltose (LB(malt)) resulted in higher cell density (OD(620) = 6.6) than use of MB(malt) (OD(620) = 1.7). Sequential batch cultivation increased the cell density threefold (OD(620) = 20) in LB(malt) and eightfold (OD(620) = 14) in MB(malt). In both single and sequential batches, the production of carotenoids and EPSs using LB(malt) was detected in the exponential phase and stationary phase, respectively, while in MB(malt) formation of both products was detectable in both the exponential and stationary phases of the culture. Heteropolymeric EPSs were produced with an overall volumetric productivity (Q(E)) of 0.67 (mg/L h) in MB(malt) and the polymer contained xylose. In LB, Q(E) was lower (0.1 mg/L h) and xylose could not be detected in the composition of the produced EPSs. In conclusion, this study showed the importance of a process design and medium source for production of R. marinus DSM 16675 and its metabolites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00792-019-01129-0) contains supplementary material, which is available to authorized users. Springer Japan 2019-09-14 2019 /pmc/articles/PMC6801211/ /pubmed/31522265 http://dx.doi.org/10.1007/s00792-019-01129-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Paper
Ron, Emanuel Y. C.
Sardari, Roya R. R.
Anthony, Richard
van Niel, Ed W. J.
Hreggvidsson, Gudmundur O.
Nordberg-Karlsson, Eva
Cultivation technology development of Rhodothermus marinus DSM 16675
title Cultivation technology development of Rhodothermus marinus DSM 16675
title_full Cultivation technology development of Rhodothermus marinus DSM 16675
title_fullStr Cultivation technology development of Rhodothermus marinus DSM 16675
title_full_unstemmed Cultivation technology development of Rhodothermus marinus DSM 16675
title_short Cultivation technology development of Rhodothermus marinus DSM 16675
title_sort cultivation technology development of rhodothermus marinus dsm 16675
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801211/
https://www.ncbi.nlm.nih.gov/pubmed/31522265
http://dx.doi.org/10.1007/s00792-019-01129-0
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