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In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
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Enzymes require additional components for proper function. There are two such classes of molecules: cofactors and coenzymes. Cofactors are metallic ions and coenzymes are non-protein organic molecules. Both of these types of helper molecule can be tightly bound to the enzyme or bound only when the substrate binds.
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Related Experiment Video

Updated: Jul 15, 2026

Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability
09:27

Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability

Published on: April 22, 2016

Cofactor regeneration at the lab scale.

R Wichmann1, D Vasic-Racki

  • 1Biochemical Engineering Group, Department of Biochemical and Chemical Engineering, Universität Dortmund, 44221 Dortmund, Germany. wichmann@bci.uni-dortmund.de

Advances in Biochemical Engineering/Biotechnology
|March 29, 2005
PubMed
Summary

Lab-scale coenzyme regeneration systems, particularly for NAD+/NADH and NADP+/NADPH, have advanced significantly. Various in situ methods, including enzymatic and electrochemical approaches, show promise for efficient biocatalysis.

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Area of Science:

  • Biotechnology
  • Biocatalysis
  • Enzyme Engineering

Background:

  • Coenzymes like NAD+/NADH and NADP+/NADPH are crucial for redox reactions in biological systems.
  • Efficient regeneration of these coenzymes is essential for cost-effective biocatalytic processes.
  • Lab-scale advancements in coenzyme regeneration have been a focus for two decades.

Purpose of the Study:

  • To review progress in lab-scale coenzyme regeneration systems.
  • To highlight NAD+/NADH and NADP+/NADPH-dependent oxidoreductase reactions.
  • To discuss various in situ regeneration strategies and enzyme reaction engineering.

Main Methods:

  • Review of in situ regeneration systems: whole cell, enzymatic, electro-enzymatic, chemical, and photochemical.
  • Analysis of efficiency and novelty of presented methods.
  • Reporting on progress in enzyme reaction engineering.

Main Results:

  • Significant progress in lab-scale coenzyme regeneration systems over the past 20 years.
  • Focus on NAD+/NADH and NADP+/NADPH-dependent oxidoreductase reactions.
  • Development and evaluation of diverse in situ regeneration techniques.

Conclusions:

  • Various coenzyme regeneration systems have been developed and assessed for lab-scale applications.
  • Enzymatic and electro-enzymatic methods show particular promise for efficient NAD+/NADH and NADP+/NADPH regeneration.
  • Continued progress in enzyme reaction engineering is vital for optimizing these systems.