Ngtet Dioxygenase

Ngtet dioxygenase is an oxygen-dependent enzyme that catalyzes the incorporation of both atoms of molecular oxygen into an organic substrate, making it a useful tool for selective chemical transformation. The enzyme binds its substrate and activates O₂ at a catalytic center, enabling oxidation reactions that can introduce hydroxyl, epoxide, or other oxygen-containing functionalities under mild conditions. In bioengineering, Ngtet dioxygenase can support metabolic pathway design, biocatalyst development, and the production or modification of valuable molecules. Understanding its substrate selectivity, reaction mechanism, and operating conditions helps researchers improve enzyme performance and develop more sustainable alternatives to conventional chemical oxidation.

Ngtet Dioxygenase - Related Videos

Research

JoVE Journal - Bioengineering

Precise Phage Mutagenesis with NgTET-Assisted CRISPR-Cas Systems

0 Views •

2025

Here, we present a protocol to reduce DNA modifications in bacteriophages using the NgTET enzyme, enabling efficient and scarless CRISPR-Cas mutagenesis. This method facilitates the genetic engineering of phages for applications in biotechnology and phage therapy.

Expression and Purification of Nuclease-Free Oxygen Scavenger Protocatechuate 3,4-Dioxygenase

0 Views •

Cited by 3 •

2019

Protocatechuate 3,4-dioxygenase (PCD) can enzymatically remove free diatomic oxygen from an aqueous system using its substrate protocatechuic acid (PCA). This protocol describes the expression, purification, and activity analysis of this oxygen scavenging enzyme.

Efficient Purification and LC-MS/MS-based Assay Development for Ten-Eleven Translocation-2 5-Methylcytosine Dioxygenase

0 Views •

Cited by 5 •

2018

Here, we present a protocol for an efficient single step purification of the active untagged human ten-eleven translocation-2 (TET2) 5-methylcytosine dioxygenase using ion-exchange chromatography and its assay using a liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based approach.

Anaerobic Protein Purification and Kinetic Analysis via Oxygen Electrode for Studying DesB Dioxygenase Activity and Inhibition

0 Views •

Cited by 3 •

2018

Here we present a protocol for anaerobic protein purification, anaerobic protein concentration, and subsequent kinetic characterization using an oxygen electrode system. The method is illustrated using the enzyme DesB, a dioxygenase enzyme which is more stable and active when purified and stored in an anaerobic environment.

Selective Enrichment and Isolation of Oil-Degrading Marine Bacteria from Seawater Samples

0 Views •

2025

Source: Villela, H. D. M., et al. Prospecting Microbial Strains for Bioremediation and Probiotics Development for Metaorganism Research and Preservation. J. Vis. Exp. (2019)This video demonstrates the selective isolation of oil-degrading marine bacteria by enriching seawater samples on oil-based media, enabling the recovery of pure strains with potential applications in crude oil bioremediation and environmental cleanup.

View All Results

FAQs

Related Topics