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The isolation of synthetic genetic polymers (XNAs) with catalytic activity demonstrates that catalysis is not limited to natural biopolymers, but it remains unknown whether such systems can achieve robust catalysis with Michaelis-Menten kinetics. Here, we describe an efficient RNA-cleaving 2'-fluoroarabino nucleic acid enzyme (FANAzyme) that functions with a rate enhancement of >10-fold over the uncatalyzed reaction and exhibits substrate saturation kinetics typical of most natural enzymes. The FANAzyme was generated by in vitro evolution using natural polymerases that were found to recognize FANA substrates with high fidelity. The enzyme comprises a small 25 nucleotide catalytic domain flanked by substrate-binding arms that can be engineered to recognize diverse RNA targets. Substrate cleavage occurs at a specific phosphodiester bond located between an unpaired guanine and a paired uracil in the substrate recognition arm. Our results expand the chemical space of nucleic acid enzymes to include nuclease-resistant scaffolds with strong catalytic activity.
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http://dx.doi.org/10.1038/s41467-018-07611-1 | DOI Listing |
Small
December 2024
Yangtze Delta Region Institute (Huzhou), University of Electronic Science and Technology of China, Huzhou, 313001, P. R. China.
In recent years, single-atom catalysts (SACs) with separated active centers and high atom utilization have grown significantly as a significant area of catalytic research. In catalytic applications, SACs of various kinds have demonstrated exceptional performance, so the study of the catalytic mechanism of SACs provides a clearer direction for the preparation of catalysts with high performance. Strong linkages between the single atoms and the support are necessary to overcome the tendency of single atoms to aggregate into clusters, which is called metal-support interaction (MSI).
View Article and Find Full Text PDFChemistry
December 2024
Shanghai University of Electric Power, College of Environmental and Chemical Engineering, 2103 Pingliang Road, Yangpu District,, 200090, Shanghai, CHINA.
Nickel-iron layered double hydroxide shows significant promise as an electrocatalyst in facilitating oxygen evolution reactions. But its development is hindered by low conductivity and insufficient cycling stability. Herein, the synthesis of a hierarchically structured heterostructure catalyst, CeO2@NiFe LDH, is reported through a straightforward two-step process involving hydrothermal treatment.
View Article and Find Full Text PDFJ Phys Chem Lett
December 2024
Toyota Central R&D Laboratories, Inc., Nagakute 480-1192, Aichi, Japan.
The modification of Pt surfaces with organic compounds like melamine enhances oxygen reduction reaction activity and catalyst durability. Through first-principles free energy calculations utilizing thermodynamic integration and finite-temperature molecular dynamics, enhanced by machine learning force fields for efficient sampling of nanosecond-scale interfacial water fluctuations and incorporating corrections to accurately reproduce first-principles free energies, we demonstrate that melamine destabilizes OH adsorbates, facilitating their removal and enhancing catalytic activity. Unlike alloys, where OH destabilization is driven by changes in electronic structure and surface strain, melamine disrupts hydrogen bonding between OH and interfacial water.
View Article and Find Full Text PDFInorg Chem
December 2024
State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources; College of Chemistry, Xinjiang University, Urumqi 830017, Xinjiang, PR China.
Piezoelectric catalytic production of HO is a novel and environmentally friendly HO production method, and many piezoelectric catalysts are currently being developed. However, all of them have the disadvantages of precious metals as cocatalysts and low catalytic efficiency. Herein, CaTiO was successfully prepared and loaded with the nonprecious metal CoP (CoP/CaTiO) for piezoelectric catalytic production of HO.
View Article and Find Full Text PDFEnviron Sci Technol
December 2024
Beijing Key Laboratory for Green Catalysis and Separation, Key Laboratory of Beijing on Regional Air Pollution Control, Key Laboratory of Advanced Functional Materials, Education Ministry of China, Laboratory of Catalysis Chemistry and Nanoscience, Department of Chemical Engineering and Technology, College of Materials Science and Engineering, Beijing University of Technology, Beijing 100124, China.
Chlorinated and oxygenated volatile organic compounds (CVOCs and OVOCs) pose a significant threat to human health. Catalytic oxidation effectively removes these pollutants, but catalyst deactivation is a challenge. Our study focused on the hydrolysis oxidation of chlorobenzene (CB) and ethyl acetate (EA) over Ru/MO/HZSM-5 (M = W, Mo).
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