Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Satagopan, Sriram, Sun, Yuan, Parquette, Jon R., Tabita, F. Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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
_version_ 1783248765267738624
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
work_keys_str_mv AT satagopansriram syntheticco2fixationenzymecascadesimmobilizedonselfassemblednanostructuresthatenhanceco2o2selectivityofrubisco
AT sunyuan syntheticco2fixationenzymecascadesimmobilizedonselfassemblednanostructuresthatenhanceco2o2selectivityofrubisco
AT parquettejonr syntheticco2fixationenzymecascadesimmobilizedonselfassemblednanostructuresthatenhanceco2o2selectivityofrubisco
AT tabitafrobert syntheticco2fixationenzymecascadesimmobilizedonselfassemblednanostructuresthatenhanceco2o2selectivityofrubisco