Literature DB >> 34985745

Cell-Free Noncanonical Redox Cofactor Systems.

William B Black1, Han Li2.   

Abstract

Noncanonical redox cofactor systems utilize nicotinamide adenine dinucleotide (phosphate), NAD(P)H, mimics to perform biotransformation reactions. Compared to systems utilizing native NAD(P)H, these noncanonical redox cofactors can offer decreased cost of cofactor supply, improved system activities, and can even supply reducing power directly to targeted reactions in complex biological environments. When these systems are operated in cell-free settings, the high level of user control afforded by direct access to the reaction system enables specific tuning of cofactor parameters, enzyme activity, and reaction progression to maximize system productivity. In this chapter, we will describe methods for constructing these cell-free noncanonical redox cofactor systems. Specifically, methods, design concepts, and system adaptation will be discussed for applying noncanonical redox cofactors to both purified protein-based and crude lysate-based biotransformation systems.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Biomimetic cofactor; Cell-free biotransformation; Crude lysate; Noncanonical redox cofactor

Mesh:

Substances:

Year:  2022        PMID: 34985745     DOI: 10.1007/978-1-0716-1998-8_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  14 in total

1.  Engineering cytochrome P450 enzymes for improved activity towards biomimetic 1,4-NADH cofactors.

Authors:  Jessica D Ryan; Richard H Fish; Douglas S Clark
Journal:  Chembiochem       Date:  2008-11-03       Impact factor: 3.164

2.  Characterization of Biomimetic Cofactors According to Stability, Redox Potentials, and Enzymatic Conversion by NADH Oxidase from Lactobacillus pentosus.

Authors:  Claudia Nowak; André Pick; Lénárd-István Csepei; Volker Sieber
Journal:  Chembiochem       Date:  2017-08-25       Impact factor: 3.164

3.  Mimicking nature: synthetic nicotinamide cofactors for C═C bioreduction using enoate reductases.

Authors:  Caroline E Paul; Serena Gargiulo; Diederik J Opperman; Iván Lavandera; Vicente Gotor-Fernández; Vicente Gotor; Andreas Taglieber; Isabel W C E Arends; Frank Hollmann
Journal:  Org Lett       Date:  2012-12-20       Impact factor: 6.005

4.  Aldehyde Production in Crude Lysate- and Whole Cell-Based Biotransformation Using a Noncanonical Redox Cofactor System.

Authors:  Kelly N Richardson; William B Black; Han Li
Journal:  ACS Catal       Date:  2020-07-23       Impact factor: 13.084

Review 5.  Biomimetic cofactors and methods for their recycling.

Authors:  Ioannis Zachos; Claudia Nowak; Volker Sieber
Journal:  Curr Opin Chem Biol       Date:  2018-10-16       Impact factor: 8.822

6.  Structure-Guided Design of Formate Dehydrogenase for Regeneration of a Non-Natural Redox Cofactor.

Authors:  Xiaojia Guo; Xueying Wang; Yuxue Liu; Qing Li; Junting Wang; Wujun Liu; Zongbao K Zhao
Journal:  Chemistry       Date:  2020-11-16       Impact factor: 5.236

7.  Virtual cofactors for an Escherichia coli nitroreductase enzyme: relevance to reductively activated prodrugs in antibody directed enzyme prodrug therapy (ADEPT).

Authors:  R J Knox; F Friedlos; M Jarman; L C Davies; P Goddard; G M Anlezark; R G Melton; R F Sherwood
Journal:  Biochem Pharmacol       Date:  1995-05-26       Impact factor: 5.858

8.  Engineering a nicotinamide mononucleotide redox cofactor system for biocatalysis.

Authors:  William B Black; Linyue Zhang; Wai Shun Mak; Sarah Maxel; Youtian Cui; Edward King; Bonnie Fong; Alicia Sanchez Martinez; Justin B Siegel; Han Li
Journal:  Nat Chem Biol       Date:  2019-11-25       Impact factor: 15.040

9.  Better than Nature: Nicotinamide Biomimetics That Outperform Natural Coenzymes.

Authors:  Tanja Knaus; Caroline E Paul; Colin W Levy; Simon de Vries; Francesco G Mutti; Frank Hollmann; Nigel S Scrutton
Journal:  J Am Chem Soc       Date:  2016-01-13       Impact factor: 15.419

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