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Creation of a functional hyperthermostable designer cellulosome

BACKGROUND: Renewable energy has become a field of high interest over the past decade, and production of biofuels from cellulosic substrates has a particularly high potential as an alternative source of energy. Industrial deconstruction of biomass, however, is an onerous, exothermic process, the cos...

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Autores principales: Kahn, Amaranta, Moraïs, Sarah, Galanopoulou, Anastasia P., Chung, Daehwan, Sarai, Nicholas S., Hengge, Neal, Hatzinikolaou, Dimitris G., Himmel, Michael E., Bomble, Yannick J., Bayer, Edward A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394049/
https://www.ncbi.nlm.nih.gov/pubmed/30858881
http://dx.doi.org/10.1186/s13068-019-1386-y
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author Kahn, Amaranta
Moraïs, Sarah
Galanopoulou, Anastasia P.
Chung, Daehwan
Sarai, Nicholas S.
Hengge, Neal
Hatzinikolaou, Dimitris G.
Himmel, Michael E.
Bomble, Yannick J.
Bayer, Edward A.
author_facet Kahn, Amaranta
Moraïs, Sarah
Galanopoulou, Anastasia P.
Chung, Daehwan
Sarai, Nicholas S.
Hengge, Neal
Hatzinikolaou, Dimitris G.
Himmel, Michael E.
Bomble, Yannick J.
Bayer, Edward A.
author_sort Kahn, Amaranta
collection PubMed
description BACKGROUND: Renewable energy has become a field of high interest over the past decade, and production of biofuels from cellulosic substrates has a particularly high potential as an alternative source of energy. Industrial deconstruction of biomass, however, is an onerous, exothermic process, the cost of which could be decreased significantly by use of hyperthermophilic enzymes. An efficient way of breaking down cellulosic substrates can also be achieved by highly efficient enzymatic complexes called cellulosomes. The modular architecture of these multi-enzyme complexes results in substrate targeting and proximity-based synergy among the resident enzymes. However, cellulosomes have not been observed in hyperthermophilic bacteria. RESULTS: Here, we report the design and function of a novel hyperthermostable “designer cellulosome” system, which is stable and active at 75 °C. Enzymes from Caldicellulosiruptor bescii, a highly cellulolytic hyperthermophilic anaerobic bacterium, were selected and successfully converted to the cellulosomal mode by grafting onto them divergent dockerin modules that can be inserted in a precise manner into a thermostable chimaeric scaffoldin by virtue of their matching cohesins. Three pairs of cohesins and dockerins, selected from thermophilic microbes, were examined for their stability at extreme temperatures and were determined stable at 75 °C for at least 72 h. The resultant hyperthermostable cellulosome complex exhibited the highest levels of enzymatic activity on microcrystalline cellulose at 75 °C, compared to those of previously reported designer cellulosome systems and the native cellulosome from Clostridium thermocellum. CONCLUSION: The functional hyperthermophilic platform fulfills the appropriate physico-chemical properties required for exothermic processes. This system can thus be adapted for other types of thermostable enzyme systems and could serve as a basis for a variety of cellulolytic and non-cellulolytic industrial objectives at high temperatures. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1386-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-63940492019-03-11 Creation of a functional hyperthermostable designer cellulosome Kahn, Amaranta Moraïs, Sarah Galanopoulou, Anastasia P. Chung, Daehwan Sarai, Nicholas S. Hengge, Neal Hatzinikolaou, Dimitris G. Himmel, Michael E. Bomble, Yannick J. Bayer, Edward A. Biotechnol Biofuels Research BACKGROUND: Renewable energy has become a field of high interest over the past decade, and production of biofuels from cellulosic substrates has a particularly high potential as an alternative source of energy. Industrial deconstruction of biomass, however, is an onerous, exothermic process, the cost of which could be decreased significantly by use of hyperthermophilic enzymes. An efficient way of breaking down cellulosic substrates can also be achieved by highly efficient enzymatic complexes called cellulosomes. The modular architecture of these multi-enzyme complexes results in substrate targeting and proximity-based synergy among the resident enzymes. However, cellulosomes have not been observed in hyperthermophilic bacteria. RESULTS: Here, we report the design and function of a novel hyperthermostable “designer cellulosome” system, which is stable and active at 75 °C. Enzymes from Caldicellulosiruptor bescii, a highly cellulolytic hyperthermophilic anaerobic bacterium, were selected and successfully converted to the cellulosomal mode by grafting onto them divergent dockerin modules that can be inserted in a precise manner into a thermostable chimaeric scaffoldin by virtue of their matching cohesins. Three pairs of cohesins and dockerins, selected from thermophilic microbes, were examined for their stability at extreme temperatures and were determined stable at 75 °C for at least 72 h. The resultant hyperthermostable cellulosome complex exhibited the highest levels of enzymatic activity on microcrystalline cellulose at 75 °C, compared to those of previously reported designer cellulosome systems and the native cellulosome from Clostridium thermocellum. CONCLUSION: The functional hyperthermophilic platform fulfills the appropriate physico-chemical properties required for exothermic processes. This system can thus be adapted for other types of thermostable enzyme systems and could serve as a basis for a variety of cellulolytic and non-cellulolytic industrial objectives at high temperatures. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1386-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-28 /pmc/articles/PMC6394049/ /pubmed/30858881 http://dx.doi.org/10.1186/s13068-019-1386-y 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. 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
Kahn, Amaranta
Moraïs, Sarah
Galanopoulou, Anastasia P.
Chung, Daehwan
Sarai, Nicholas S.
Hengge, Neal
Hatzinikolaou, Dimitris G.
Himmel, Michael E.
Bomble, Yannick J.
Bayer, Edward A.
Creation of a functional hyperthermostable designer cellulosome
title Creation of a functional hyperthermostable designer cellulosome
title_full Creation of a functional hyperthermostable designer cellulosome
title_fullStr Creation of a functional hyperthermostable designer cellulosome
title_full_unstemmed Creation of a functional hyperthermostable designer cellulosome
title_short Creation of a functional hyperthermostable designer cellulosome
title_sort creation of a functional hyperthermostable designer cellulosome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394049/
https://www.ncbi.nlm.nih.gov/pubmed/30858881
http://dx.doi.org/10.1186/s13068-019-1386-y
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