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meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H01:13

meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H

All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for the...
Role of Reduced Coenzymes NADH and FADH₂01:29

Role of Reduced Coenzymes NADH and FADH₂

The energy released from the breakdown of the chemical bonds within nutrients can be stored either through the reduction of electron carriers or in the bonds of adenosine triphosphate (ATP). In living systems, a small class of compounds functions as mobile electron carriers, molecules that bind to and shuttle high-energy electrons between compounds in pathways. The principal electron carriers that will be considered originate from the B vitamin group and are derivatives of nucleotides; they are...
Inorganic Nitrogen Assimilation01:22

Inorganic Nitrogen Assimilation

Nitrogen is an essential element in biological systems, forming a crucial component of proteins, nucleic acids, and other cellular constituents. Many bacteria and archaea acquire nitrogen in the form of nitrate (NO₃⁻) or ammonia (NH₃), which are then assimilated into biomolecules through specific enzymatic pathways.Assimilatory Nitrate ReductionWhen nitrate enters the cell, it undergoes a two-step reduction process known as assimilatory nitrate reduction. Initially, the enzyme nitrate reductase...
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
Carbon-dioxide Fixation01:28

Carbon-dioxide Fixation

Carbon dioxide fixation in prokaryotes enables the assimilation of inorganic carbon into organic molecules, supporting biosynthetic pathways, sustaining ecosystems, and contributing to the global carbon cycle. It also has industrial applications in carbon capture and bioproduct synthesis. Autotrophic organisms rely on this process to utilize CO₂ as a carbon source in diverse environments.The Calvin CycleThe Calvin cycle is the most widespread carbon fixation mechanism, primarily used by...
Overview of Nitrogen Metabolism01:20

Overview of Nitrogen Metabolism

Nitrogen is a very important element for life because it is a major constituent of proteins and nucleic acids. It is a macronutrient, and in nature, it is recycled from organic compounds and stored in the form of  ammonia, ammonium ions, nitrate, nitrite, or  nitrogen gas by many metabolic processes. Many of these metabolic processes are carried out only by prokaryotes.
The largest pool of nitrogen available in the terrestrial ecosystem is gaseous nitrogen (N2) from the air, but this nitrogen...

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Updated: Jun 10, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
10:57

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

La nitrogenasa de vanadio reduce el CO.

Chi Chung Lee1, Yilin Hu, Markus W Ribbe

  • 1Department of Molecular Biology and Biochemistry, University of California, Irvine, CA 92697-3900, USA.

Science (New York, N.Y.)
|August 7, 2010
PubMed
Resumen
Este resumen es generado por máquina.

La vanadium nitrogenase convierte el dinitrógeno en amoníaco y el monóxido de carbono en hidrocarburos. Esto sugiere un vínculo evolutivo y mecanicista compartido entre los ciclos de carbono y nitrógeno de la Tierra.

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Área de la Ciencia:

  • La bioquímica es la bioquímica.
  • Ciencias del medio ambiente Ciencias del medio ambiente.
  • La geoquímica es la geoquímica.

Sus antecedentes:

  • Las enzimas nitrogenasas son cruciales para convertir el nitrógeno atmosférico en amoníaco, un proceso vital para la vida.
  • La nitrogenasa dependiente de vanadio (V-nitrogenasa) es una variante única con un sitio activo distinto.
  • Las capacidades catalíticas de la V-nitrogenasa más allá de la reducción de nitrógeno no se comprenden completamente.

Objetivo del estudio:

  • Investigar las capacidades reductoras de la vanadio nitrogenasa más allá de su papel conocido en la fijación del nitrógeno.
  • Explorar el potencial de la V-nitrogenasa para catalizar la reducción del monóxido de carbono.
  • Evaluar las implicaciones de estos hallazgos para comprender la interacción entre los ciclos de carbono y nitrógeno.

Principales métodos:

  • Los ensayos enzimáticos se realizaron utilizando nitrogenasas de vanadio purificadas.
  • Se realizaron experimentos de reducción de sustrato con dinitrógeno y monóxido de carbono en condiciones controladas.
  • El análisis del producto se llevó a cabo utilizando cromatografía de gases.

Principales resultados:

  • La vanadium nitrogenase reduce eficientemente el dinitrógeno a amoníaco.
  • La enzima también catalizó la reducción del monóxido de carbono a etileno, etano y propano.
  • Los productos de hidrocarburos observados indican una vía de reducción compleja.

Conclusiones:

  • La vanadio nitrogenasa posee un rango de sustrato más amplio de lo que se reconocía anteriormente, incluida la reducción de monóxido de carbono.
  • La doble funcionalidad en la reducción tanto de N2 como de CO sugiere una posible conexión mecánica y evolutiva entre los ciclos de nitrógeno y carbono.
  • Este hallazgo abre nuevas vías para explorar la catálisis de inspiración biológica y los primeros procesos biogeoquímicos de la Tierra.