Reprint

Enzyme Catalysis: Advances, Techniques, and Outlooks

Edited by
August 2022
88 pages
  • ISBN978-3-0365-5087-9 (Hardback)
  • ISBN978-3-0365-5088-6 (PDF)

This book is a reprint of the Special Issue Enzyme Catalysis: Advances, Techniques, and Outlooks that was published in

Biology & Life Sciences
Chemistry & Materials Science
Computer Science & Mathematics
Engineering
Environmental & Earth Sciences
Physical Sciences
Summary

Enzyme-mediated catalysis offers special advantages over chemical methods. First of all, enzymes are considered an environmentally friendly tool as they help to avoid the requirements of toxic chemicals and high energy. In addition, more feasible processes can be accomplished through enzymatic reactions owing to the enzyme’s innate properties related to high substrate specificity and selectivity. For this reason, biotechnological production of a wide range of products, such as alternative fuels and value-added biochemicals, has been commercially applicable with the aid of enzymes, either in isolated form or in the whole-cell system. In particular, enzymatic transformation of low-value but cheap/abundant starting materials (i.g. biomass) into high-value materials can facilitate the circular and sustainable bioeconomy. This Special Issue on “Enzyme Catalysis: Advances, Techniques, and Outlooks” consists of six articles, which address diverse industrially relevant enzymes with applications in foods, detergent, cosmetics, medicine, etc. A robust methodology related to enzyme kinetics is also addressed.

Format
  • Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
CYP102A1; atorvastatin; 4-hydroxy atorvastatin; hydrogen peroxide; P450 peroxygenase; NADPH; enzyme inhibition; integrated Michaelis–Menten equations; reaction product inhibition; two mutually exclusive inhibitors; protease; detergent; surfactant; cleaning; glucose isomerase; xylose isomerase; high-fructose corn syrup; HFCS; bioethanol; structure; l-fucose isomerase; l-fucose; l-fuculose; extremophile; halothermophilic bacteria; Halothermothrix orenii; lysozyme; muramidase; N-acetylmuramide glycanhydrolase; human; N-acetyl-β-d-glucosaminidase; NAG; crystal structure; n/a