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Process relevant screening of cellulolytic organisms for consolidated bioprocessing

BACKGROUND: Although the biocatalytic conversion of cellulosic biomass could replace fossil oil for the production of various compounds, it is often not economically viable due to the high costs of cellulolytic enzymes. One possibility to reduce costs is consolidated bioprocessing (CBP), integrating...

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Autores principales: Antonov, Elena, Schlembach, Ivan, Regestein, Lars, Rosenbaum, Miriam A., Büchs, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402656/
https://www.ncbi.nlm.nih.gov/pubmed/28450887
http://dx.doi.org/10.1186/s13068-017-0790-4
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author Antonov, Elena
Schlembach, Ivan
Regestein, Lars
Rosenbaum, Miriam A.
Büchs, Jochen
author_facet Antonov, Elena
Schlembach, Ivan
Regestein, Lars
Rosenbaum, Miriam A.
Büchs, Jochen
author_sort Antonov, Elena
collection PubMed
description BACKGROUND: Although the biocatalytic conversion of cellulosic biomass could replace fossil oil for the production of various compounds, it is often not economically viable due to the high costs of cellulolytic enzymes. One possibility to reduce costs is consolidated bioprocessing (CBP), integrating cellulase production, hydrolysis of cellulose, and the fermentation of the released sugars to the desired product into one process step. To establish such a process, the most suitable cellulase-producing organism has to be identified. Thereby, it is crucial to evaluate the candidates under target process conditions. In this work, the chosen model process was the conversion of cellulose to the platform chemical itaconic acid by a mixed culture of a cellulolytic fungus with Aspergillus terreus as itaconic acid producer. Various cellulase producers were analyzed by the introduced freeze assay that measures the initial carbon release rate, quantifying initial cellulase activity under target process conditions. Promising candidates were then characterized online by monitoring their respiration activity metabolizing cellulose to assess the growth and enzyme production dynamics. RESULTS: The screening of five different cellulase producers with the freeze assay identified Trichoderma reesei and Penicillium verruculosum as most promising. The measurement of the respiration activity revealed a retarded induction of cellulase production for P. verruculosum but a similar cellulase production rate afterwards, compared to T. reesei. The freeze assay measurement depicted that P. verruculosum reaches the highest initial carbon release rate among all investigated cellulase producers. After a modification of the cultivation procedure, these results were confirmed by the respiration activity measurement. To compare both methods, a correlation between the measured respiration activity and the initial carbon release rate of the freeze assay was introduced. The analysis revealed that the different initial enzyme/cellulose ratios as well as a discrepancy in cellulose digestibility are the main differences between the two approaches. CONCLUSIONS: With two complementary methods to quantify cellulase activity and the dynamics of cellulase production for CBP applications, T. reesei and P. verruculosum were identified as compatible candidates for the chosen model process. The presented methods can easily be adapted to screen for suitable cellulose degrading organisms for various other applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0790-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-54026562017-04-27 Process relevant screening of cellulolytic organisms for consolidated bioprocessing Antonov, Elena Schlembach, Ivan Regestein, Lars Rosenbaum, Miriam A. Büchs, Jochen Biotechnol Biofuels Research BACKGROUND: Although the biocatalytic conversion of cellulosic biomass could replace fossil oil for the production of various compounds, it is often not economically viable due to the high costs of cellulolytic enzymes. One possibility to reduce costs is consolidated bioprocessing (CBP), integrating cellulase production, hydrolysis of cellulose, and the fermentation of the released sugars to the desired product into one process step. To establish such a process, the most suitable cellulase-producing organism has to be identified. Thereby, it is crucial to evaluate the candidates under target process conditions. In this work, the chosen model process was the conversion of cellulose to the platform chemical itaconic acid by a mixed culture of a cellulolytic fungus with Aspergillus terreus as itaconic acid producer. Various cellulase producers were analyzed by the introduced freeze assay that measures the initial carbon release rate, quantifying initial cellulase activity under target process conditions. Promising candidates were then characterized online by monitoring their respiration activity metabolizing cellulose to assess the growth and enzyme production dynamics. RESULTS: The screening of five different cellulase producers with the freeze assay identified Trichoderma reesei and Penicillium verruculosum as most promising. The measurement of the respiration activity revealed a retarded induction of cellulase production for P. verruculosum but a similar cellulase production rate afterwards, compared to T. reesei. The freeze assay measurement depicted that P. verruculosum reaches the highest initial carbon release rate among all investigated cellulase producers. After a modification of the cultivation procedure, these results were confirmed by the respiration activity measurement. To compare both methods, a correlation between the measured respiration activity and the initial carbon release rate of the freeze assay was introduced. The analysis revealed that the different initial enzyme/cellulose ratios as well as a discrepancy in cellulose digestibility are the main differences between the two approaches. CONCLUSIONS: With two complementary methods to quantify cellulase activity and the dynamics of cellulase production for CBP applications, T. reesei and P. verruculosum were identified as compatible candidates for the chosen model process. The presented methods can easily be adapted to screen for suitable cellulose degrading organisms for various other applications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0790-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-24 /pmc/articles/PMC5402656/ /pubmed/28450887 http://dx.doi.org/10.1186/s13068-017-0790-4 Text en © The Author(s) 2017 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Antonov, Elena
Schlembach, Ivan
Regestein, Lars
Rosenbaum, Miriam A.
Büchs, Jochen
Process relevant screening of cellulolytic organisms for consolidated bioprocessing
title Process relevant screening of cellulolytic organisms for consolidated bioprocessing
title_full Process relevant screening of cellulolytic organisms for consolidated bioprocessing
title_fullStr Process relevant screening of cellulolytic organisms for consolidated bioprocessing
title_full_unstemmed Process relevant screening of cellulolytic organisms for consolidated bioprocessing
title_short Process relevant screening of cellulolytic organisms for consolidated bioprocessing
title_sort process relevant screening of cellulolytic organisms for consolidated bioprocessing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402656/
https://www.ncbi.nlm.nih.gov/pubmed/28450887
http://dx.doi.org/10.1186/s13068-017-0790-4
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