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Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO
BACKGROUND: With increasing concerns over global warming and depletion of fossil-fuel reserves, it is attractive to develop innovative strategies to assimilate CO(2), a greenhouse gas, into usable organic carbon. Cell-free systems can be designed to operate as catalytic platforms with enzymes that o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501267/ https://www.ncbi.nlm.nih.gov/pubmed/28694846 http://dx.doi.org/10.1186/s13068-017-0861-6 |
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author | Satagopan, Sriram Sun, Yuan Parquette, Jon R. Tabita, F. Robert |
author_facet | Satagopan, Sriram Sun, Yuan Parquette, Jon R. Tabita, F. Robert |
author_sort | Satagopan, Sriram |
collection | PubMed |
description | BACKGROUND: With increasing concerns over global warming and depletion of fossil-fuel reserves, it is attractive to develop innovative strategies to assimilate CO(2), a greenhouse gas, into usable organic carbon. Cell-free systems can be designed to operate as catalytic platforms with enzymes that offer exceptional selectivity and efficiency, without the need to support ancillary reactions of metabolic pathways operating in intact cells. Such systems are yet to be exploited for applications involving CO(2) utilization and subsequent conversion to valuable products, including biofuels. The Calvin–Benson–Bassham (CBB) cycle and the enzyme ribulose 1,5-bisphosphate carboxylase/oxygenase (RubisCO) play a pivotal role in global CO(2) fixation. RESULTS: We hereby demonstrate the co-assembly of two RubisCO-associated multienzyme cascades with self-assembled synthetic amphiphilic peptide nanostructures. The immobilized enzyme cascades sequentially convert either ribose-5-phosphate (R-5-P) or glucose, a simpler substrate, to ribulose 1,5-bisphosphate (RuBP), the acceptor for incoming CO(2) in the carboxylation reaction catalyzed by RubisCO. Protection from proteolytic degradation was observed in nanostructures associated with the small dimeric form of RubisCO and ancillary enzymes. Furthermore, nanostructures associated with a larger variant of RubisCO resulted in a significant enhancement of the enzyme’s selectivity towards CO(2), without adversely affecting the catalytic activity. CONCLUSIONS: The ability to assemble a cascade of enzymes for CO(2) capture using self-assembling nanostructure scaffolds with functional enhancements show promise for potentially engineering entire pathways (with RubisCO or other CO(2)-fixing enzymes) to redirect carbon from industrial effluents into useful bioproducts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0861-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5501267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55012672017-07-10 Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO Satagopan, Sriram Sun, Yuan Parquette, Jon R. Tabita, F. Robert Biotechnol Biofuels Research BACKGROUND: With increasing concerns over global warming and depletion of fossil-fuel reserves, it is attractive to develop innovative strategies to assimilate CO(2), a greenhouse gas, into usable organic carbon. Cell-free systems can be designed to operate as catalytic platforms with enzymes that offer exceptional selectivity and efficiency, without the need to support ancillary reactions of metabolic pathways operating in intact cells. Such systems are yet to be exploited for applications involving CO(2) utilization and subsequent conversion to valuable products, including biofuels. The Calvin–Benson–Bassham (CBB) cycle and the enzyme ribulose 1,5-bisphosphate carboxylase/oxygenase (RubisCO) play a pivotal role in global CO(2) fixation. RESULTS: We hereby demonstrate the co-assembly of two RubisCO-associated multienzyme cascades with self-assembled synthetic amphiphilic peptide nanostructures. The immobilized enzyme cascades sequentially convert either ribose-5-phosphate (R-5-P) or glucose, a simpler substrate, to ribulose 1,5-bisphosphate (RuBP), the acceptor for incoming CO(2) in the carboxylation reaction catalyzed by RubisCO. Protection from proteolytic degradation was observed in nanostructures associated with the small dimeric form of RubisCO and ancillary enzymes. Furthermore, nanostructures associated with a larger variant of RubisCO resulted in a significant enhancement of the enzyme’s selectivity towards CO(2), without adversely affecting the catalytic activity. CONCLUSIONS: The ability to assemble a cascade of enzymes for CO(2) capture using self-assembling nanostructure scaffolds with functional enhancements show promise for potentially engineering entire pathways (with RubisCO or other CO(2)-fixing enzymes) to redirect carbon from industrial effluents into useful bioproducts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0861-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-06 /pmc/articles/PMC5501267/ /pubmed/28694846 http://dx.doi.org/10.1186/s13068-017-0861-6 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 Satagopan, Sriram Sun, Yuan Parquette, Jon R. Tabita, F. Robert Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO |
title | Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO |
title_full | Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO |
title_fullStr | Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO |
title_full_unstemmed | Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO |
title_short | Synthetic CO(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO(2)/O(2) selectivity of RubisCO |
title_sort | synthetic co(2)-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance co(2)/o(2) selectivity of rubisco |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501267/ https://www.ncbi.nlm.nih.gov/pubmed/28694846 http://dx.doi.org/10.1186/s13068-017-0861-6 |
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