Design of a Synthetic Enzyme Cascade for the in vitro Fixation of a C1 Carbon Source to a Functional C4 Sugar

2021 ◽  
Author(s):  
Samed Güner ◽  
Vanessa Wegat ◽  
André Pick ◽  
Volker Sieber
Keyword(s):  
Carbon Dioxide ◽  
Carbon Source ◽  
Greenhouse Gas ◽  
Value Added ◽  
Waste Stream ◽  
Enzyme Cascade ◽  
Sustainable Future ◽  
Value Added Products

Realizing a sustainable future requires intensifying the waste stream conversion, such as converting the greenhouse gas carbon dioxide into value-added products. In this paper, we focus on utilizing formaldehyde as...

CuAg nanoparticles/carbon aerogel for electrochemical CO2 reduction

2021 ◽  
Author(s):  
Wenbo Wang ◽  
Runqing Lu ◽  
Xin-Xin Xiao ◽  
Shanhe Gong ◽  
Daniel Kobina Sam ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Greenhouse Gas ◽  
Co2 Reduction ◽  
Value Added ◽  
Electrical Energy ◽  
Carbon Aerogel ◽  
Carbon Dioxide Reduction ◽  
Reduction Reaction ◽  
Electrochemical Co2 Reduction ◽  
Value Added Products

Electrochemical carbon dioxide reduction reaction (eCO2RR) is a promising technology that uses electrical energy to catalytically reduce the greenhouse gas-CO2, which can convert CO2 into high value-added products such as...

scholarly journals Conversion of stranded waste-stream carbon and nutrients into value-added products via metabolically coupled binary heterotroph-photoautotroph system

2018 ◽  
Vol 260 ◽  
pp. 68-75 ◽  
Author(s):  
Pavlo Bohutskyi ◽  
Leo A. Kucek ◽  
Eric Hill ◽  
Grigoriy E. Pinchuk ◽  
Sagadevan G. Mundree ◽  
...  
Keyword(s):  
Value Added ◽  
Waste Stream ◽  
Value Added Products

scholarly journals Biosynthesis of Polyhydroxyalkanoate Terpolymer from Methanol via the Reverse β-Oxidation Pathway in the Presence of Lanthanide

2022 ◽  
Vol 10 (1) ◽  
pp. 184
Author(s):  
Izumi Orita ◽  
Gento Unno ◽  
Risa Kato ◽  
Toshiaki Fukui
Keyword(s):  
Carbon Source ◽  
Sole Carbon Source ◽  
Ralstonia Eutropha ◽  
Negative Impact ◽  
Value Added ◽  
Pha Synthase ◽  
Growth Impairment ◽  
Oxidation Pathway ◽  
Methylotrophic Growth ◽  
Value Added Products

Methylorubrum extorquens AM1 is the attractive platform for the production of value-added products from methanol. We previously demonstrated that M. extorquens equipped with PHA synthase with broad substrate specificity synthesized polyhydroxyalkanoates (PHAs) composed of (R)-3-hydroxybutyrate and small fraction of (R)-3-hydroxyvalerate (3HV) and (R)-3-hydroxyhexanoate (3HHx) units on methanol. This study further engineered M. extorquens for biosynthesis of PHAs with higher 3HV and 3HHx composition focusing on the EMC pathway involved in C1 assimilation. The introduction of ethylmalonyl-CoA decarboxylase, catalyzing a backward reaction in the EMC pathway, aiming to increase intracellular propionyl/butyryl-CoA precursors did not affect PHA composition. Reverse b-oxidation pathway and subsequent (R)-specific hydration of 2-enoyl-CoA were then enhanced by heterologous expression of four genes derived from Ralstonia eutropha for the conversion of propionyl/butyryl-CoAs to the corresponding (R)-3-hydroxyacyl-CoA monomers. The resulting strains produced PHAs with higher 3HV and 3HHx compositions, while the methylotrophic growth was severely impaired. This growth impairment was interestingly restored by the addition of La3+ without a negative impact on PHA biosynthesis, suggesting the activation of the EMC pathway by La3+. The engineered M. extorquens synthesized PHA terpolymer composed of 5.4 mol% 3HV and 0.9% of 3HHx with 41% content from methanol as a sole carbon source in the presence of La3+.

Salen ligand complexes as electrocatalysts for direct electrochemical reduction of gaseous carbon dioxide to value added products

RSC Advances ◽  
2015 ◽  
Vol 5 (5) ◽  
pp. 3581-3589 ◽  
Author(s):  
Surya Singh ◽  
Bedika Phukan ◽  
Chandan Mukherjee ◽  
Anil Verma
Keyword(s):  
Carbon Dioxide ◽  
Electrochemical Reduction ◽  
Value Added ◽  
Salen Complexes ◽  
Gaseous Carbon Dioxide ◽  
Salen Ligand ◽  
Centrosymmetric Molecule ◽  
Value Added Products

CO2, being a linear and centrosymmetric molecule, is very stable, and the electrochemical reduction of CO2 requires energy. However, the salen complexes are found to be very efficient to minimize overpotential as compared to their metal counterparts.

scholarly journals Positional effects of second-sphere amide pendants on electrochemical CO2 reduction catalyzed by iron porphyrins

2018 ◽  
Vol 9 (11) ◽  
pp. 2952-2960 ◽  
Author(s):  
Eva M. Nichols ◽  
Jeffrey S. Derrick ◽  
Sepand K. Nistanaki ◽  
Peter T. Smith ◽  
Christopher J. Chang
Keyword(s):  
Carbon Dioxide ◽  
Greenhouse Gas ◽  
Electrochemical Reduction ◽  
Energy Input ◽  
Sustainable Energy ◽  
Co2 Reduction ◽  
Value Added ◽  
Iron Porphyrins ◽  
Electrochemical Co2 Reduction ◽  
Positional Effects

The development of catalysts for electrochemical reduction of carbon dioxide offers an attractive approach to transforming this greenhouse gas into value-added carbon products with sustainable energy input.

scholarly journals Electrocatalytic Processes for the Valorization of CO2: Synthesis of Cyanobenzoic Acid Using Eco-Friendly Strategies

Catalysts ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 413 ◽  
Author(s):  
Silvia Mena ◽  
Iluminada Gallardo ◽  
Gonzalo Guirado
Keyword(s):  
Carbon Dioxide ◽  
Global Warming ◽  
Electrochemical Techniques ◽  
Value Added ◽  
Green Technology ◽  
Green Solvents ◽  
Silver Cathodes ◽  
Carbon Dioxide Co2 ◽  
Environmentally Friendly Process ◽  
Value Added Products

Carbon dioxide (CO2) is a known greenhouse gas, and is the most important contributor to global warming. Therefore, one of the main challenges is to either eliminate or reuse it through the synthesis of value-added products, such as carboxylated derivatives. One of the most promising approaches for activating, capturing, and valorizing CO2 is the use of electrochemical techniques. In the current manuscript, we described an electrocarboxylation route for synthesizing 4-cyanobenzoic acid by valorizing CO2 through the synergistic use of electrochemical techniques (“green technology”) and ionic liquids (ILs) (“green solvents”)—two of the major entries in the general green chemistry tool kit. Moreover, the use of silver cathodes and ILs enabled the electrochemical potential applied to be reduced by more than 0.4 V. The “green” synthesis of those derivatives would provide a suitable environmentally friendly process for the design of plasticizers based on phthalate derivatives.

scholarly journals Exploiting xylan as sugar donor for the synthesis of an antiproliferative xyloside using an enzyme cascade

2019 ◽  
Vol 18 (1) ◽  
Author(s):  
Manuel Nieto-Domínguez ◽  
José Alberto Martínez-Fernández ◽  
Beatriz Fernández de Toro ◽  
Juan A. Méndez-Líter ◽  
Francisco Javier Cañada ◽  
...  
Keyword(s):  
Chemical Synthesis ◽  
Biomass Conversion ◽  
Value Added ◽  
Cost Effective ◽  
Raw Material ◽  
Birchwood Xylan ◽  
Enzyme Cascade ◽  
Antiproliferative Agent ◽  
Xylanolytic Enzymes ◽  
Value Added Products

Abstract Background Currently, industrial societies are seeking for green alternatives to conventional chemical synthesis. This demand has merged with the efforts to convert lignocellulosic biomass into value-added products. In this context, xylan, as one of main components of lignocellulose, has emerged as a raw material with high potential for advancing towards a sustainable economy. Results In this study, the recombinant endoxylanase rXynM from the ascomycete Talaromyces amestolkiae has been heterologously expressed in Pichia pastoris and used as one of the catalysts of an enzyme cascade developed to synthesize the antiproliferative 2-(6-hydroxynaphthyl) β-d-xylopyranoside, by transglycosylation of 2,6-dihydroxynaphthalene. The approach combines the use of two fungal xylanolytic enzymes, rXynM and the β-xylosidase rBxTW1 from the same fungus, with the cost-effective substrate xylan. The reaction conditions for the cascade were optimized by a Central Composite Design. Maximal productions of 0.59 and 0.38 g/L were reached using beechwood xylan and birchwood xylan, respectively. For comparison, xylans from other sources were tested in the same reaction, suggesting that a specific optimization is required for each xylan variety. The results obtained using this enzyme cascade and xylan were similar or better to those previously reported for a single catalyst and xylobiose, an expensive sugar donor. Conclusions Beechwood and birchwood xylan, two polysaccharides easily available from biomass, were used in a novel enzyme cascade to synthetize an antiproliferative agent. The approach represents a green alternative to the conventional chemical synthesis of 2-(6-hydroxynaphthyl) β-d-xylopyranoside using a cost-effective substrate. The work highlights the role of xylan as a raw material for producing value-added products and the potential of fungal xylanolytic enzymes in the biomass conversion.

scholarly journals Photoelectrochemical Conversion of Carbon Dioxide (CO2) into Fuels and Value-Added Products

2020 ◽  
Vol 5 (2) ◽  
pp. 486-519 ◽  
Author(s):  
Vignesh Kumaravel ◽  
John Bartlett ◽  
Suresh C. Pillai
Keyword(s):  
Carbon Dioxide ◽  
Value Added ◽  
Carbon Dioxide Co2 ◽  
Value Added Products

scholarly journals Elucidation of the Roles of Ionic Liquid in CO2 Electrochemical Reduction to Value-Added Chemicals and Fuels

Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6962
Author(s):  
Sulafa Abdalmageed Saadaldeen Mohammed ◽  
Wan Zaireen Nisa Yahya ◽  
Mohamad Azmi Bustam ◽  
Md Golam Kibria
Keyword(s):  
Carbon Dioxide ◽  
Ionic Liquids ◽  
Reaction Mechanism ◽  
Electrochemical Reduction ◽  
Value Added ◽  
Faradaic Efficiency ◽  
Renewable Source ◽  
Carbon Dioxide Co2 ◽  
Physical And Chemical ◽  
Value Added Products

The electrochemical reduction of carbon dioxide (CO2ER) is amongst one the most promising technologies to reduce greenhouse gas emissions since carbon dioxide (CO2) can be converted to value-added products. Moreover, the possibility of using a renewable source of energy makes this process environmentally compelling. CO2ER in ionic liquids (ILs) has recently attracted attention due to its unique properties in reducing overpotential and raising faradaic efficiency. The current literature on CO2ER mainly reports on the effect of structures, physical and chemical interactions, acidity, and the electrode–electrolyte interface region on the reaction mechanism. However, in this work, new insights are presented for the CO2ER reaction mechanism that are based on the molecular interactions of the ILs and their physicochemical properties. This new insight will open possibilities for the utilization of new types of ionic liquids. Additionally, the roles of anions, cations, and the electrodes in the CO2ER reactions are also reviewed.

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