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Related Concept Videos

Nitriles to Carboxylic Acids: Hydrolysis01:08

Nitriles to Carboxylic Acids: Hydrolysis

Nitriles undergo acid-catalyzed hydrolysis or base-catalyzed hydrolysis to form a carboxylic acid. These reactions proceed via an amide intermediate.
Preparation of Nitriles01:12

Preparation of Nitriles

One of the common methods to prepare nitriles is the dehydration of amides. This method requires strong dehydrating agents like phosphorous pentoxide or boiling acetic anhydride for converting amides to nitriles. Another reagent namely, thionyl chloride also accomplishes the dehydration of amides, where amide acts as a nucleophile. The first step of the mechanism involves the nucleophilic attack by the amide on the thionyl chloride to form an intermediate. In the next step, the electron pairs...
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...
Preparation of Amines: Reduction of Oximes and Nitro Compounds01:29

Preparation of Amines: Reduction of Oximes and Nitro Compounds

Oximes can be reduced to primary amines using catalytic hydrogenation, hydride reduction, or sodium metal reduction. The reduction of aliphatic and aromatic nitro compounds to primary amines takes place by either catalytic hydrogenation or by using active metals like Fe, Zn, and Sn in the presence of an acid.
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Nitriles to Ketones: Grignard Reaction00:57

Nitriles to Ketones: Grignard Reaction

Organomagnesium halides, commonly known as Grignard reagents, convert nitriles to ketones and proceed through a nucleophilic acyl substitution. Nitriles react with a Grignard reagent, followed by an aqueous acid, to yield ketones. The reaction introduces a new carbon–carbon bond. The alkyl–magnesium bond in the Grignard reagent is highly polar, so the alkyl carbon develops a carbanionic character and acts as a nucleophile.
The mechanism begins with a nucleophilic attack by the Grignard reagent...
Nitrosation of Enols01:19

Nitrosation of Enols

The nitrosation reaction is one of the methods of preparing 1,2-diketones. The enol tautomer of the starting ketone reacts with sodium nitrite in hydrochloric acid, generating the 1,2-diketone after hydrolysis.

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Related Experiment Video

Updated: May 17, 2026

A Direct, Regioselective and Atom-Economical Synthesis of 3-Aroyl-N-hydroxy-5-nitroindoles by Cycloaddition of 4-Nitronitrosobenzene with Alkynones
07:30

A Direct, Regioselective and Atom-Economical Synthesis of 3-Aroyl-N-hydroxy-5-nitroindoles by Cycloaddition of 4-Nitronitrosobenzene with Alkynones

Published on: January 21, 2020

Nitrilases in nitrile biocatalysis: recent progress and forthcoming research.

Jin-Song Gong1, Zhen-Ming Lu, Heng Li

  • 1The Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi, People's Republic of China.

Microbial Cell Factories
|October 31, 2012
PubMed
Summary
This summary is machine-generated.

Nitrilases are versatile biocatalysts from various organisms, crucial for nitrile degradation and industrial applications like carboxylic acid production. Further research and development are ongoing for enhanced catalytic capabilities.

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Area of Science:

  • Biochemistry
  • Enzymology
  • Industrial Biotechnology

Background:

  • Nitrilases are enzymes widely studied for their role in nitrile degradation.
  • These biocatalysts are sourced from diverse organisms including bacteria, fungi, yeasts, and plants.
  • Significant research has focused on their mechanisms, structure, and screening.

Purpose of the Study:

  • To provide a comprehensive review of the current state of nitrilase research.
  • To discuss the challenges and advancements in the development of nitrilases.
  • To highlight the potential of nitrilases as industrial biocatalysts.

Main Methods:

  • Literature review of nitrilase research over recent decades.
  • Analysis of studies on nitrilase sources, functions, and properties.
  • Examination of research on enzyme modification, immobilization, and purification.

Main Results:

  • Nitrilases are effective biocatalysts for nitrile degradation and carboxylic acid production.
  • Commercial applications include waste treatment and surface modification.
  • Ongoing research addresses enzyme engineering and process optimization.

Conclusions:

  • Nitrilases represent a significant and promising class of biocatalysts for various catalytic applications.
  • Further development is essential to fully exploit their industrial potential.
  • Continued investigation into nitrilase properties and applications is warranted.